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Clare Hall, Cambridge and LUT University, Finland sign agreement on fellowships and global climate prize

Tue, 28/05/2024 - 16:11

Clare Hall, Cambridge and LUT University, Finland, establish a Visiting Fellowship programme and joint Global Prize for Solutions to Climate Change Threats. Please read more about this story here

We very much look forward to welcoming high-flying academics from LUT over the years to come to our unique interdisciplinary research communityClare Hall President Alan ShortCredit/Clare HallLUT Rector Juha-Matti Saksa and Clare Hall President President Alan Short and signing the joint agreement

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YesLicence type: Public Domain

Cambridge research receives £5 million boost for ‘world-leading’ cardiovascular research

Tue, 28/05/2024 - 12:10

The funding will support the university to cultivate a world-class research environment that encourages collaboration, inclusion and innovation, and where visionary scientists can drive lifesaving breakthroughs.

Professor Martin Bennett, BHF Professor of Cardiovascular Sciences at the University of Cambridge, said: “This is a fantastic achievement from the whole Cambridge team. This award will support our multiple research programmes identifying new targets and treatments for vascular disease and heart failure, new ways to reduce the consequences of diabetes and obesity, and how we can get our research used to treat patients.”

The Cambridge award is part of a £35 million boost to UK cardiovascular disease research from the British Heart Foundation. It comes from the charity’s highly competitive Research Excellence Awards funding scheme. The £5 million award to the University of Cambridge will support researchers to:

Combine their expertise to work on cardiovascular diseases and in populations with high unmet need.
Identify new markers and disease targets for a wide range of cardiovascular diseases, and test new drugs in clinical trials.
Develop new ways to diagnose cardiovascular disease and harness the power of artificial intelligence from imaging and health records to identify people at highest risk.
Generate user-friendly risk communication and management tools to improve the prevention and management of cardiovascular disease.

Professor Bryan Williams, Chief Scientific and Medical Officer at the British Heart Foundation, said: “We’re delighted to continue to support research at the University of Cambridge addressing the biggest challenges in cardiovascular disease. This funding recognises the incredible research happening at Cambridge and will help to further its reputation as a global leader in the field.

“With generous donations from our supporters, this funding will attract the brightest talent, power cutting-edge science, and unlock lifesaving discoveries that can turn the tide on the devastation caused by heart and circulatory diseases.”

Research Excellence Awards offer greater flexibility than traditional research funding, allowing scientists to quickly launch ambitious projects that can act as a springboard for larger, transformative funding applications.

The funding also aims to break down the silos that have traditionally existed in research, encouraging collaboration between experts from diverse fields. From clinicians to data scientists, biologists to engineers, the funding will support universities to attract the brightest minds, nurture new talent and foster collaboration to answer the biggest questions in heart and circulatory disease research.

The University of Cambridge has previously been awarded £9 million funding through the BHF’s Research Excellence Awards scheme. This funding has supported research that will lay the foundations for future breakthroughs, including:

Research showing that low doses of a cancer drug could improve recovery after a heart attack. The drug boosts activity of anti-inflammatory immune cells that can cause harmful inflammation in blood vessels supplying the heart. It’s currently being tested in clinical trials to see if it benefits patients.
A new risk calculator to enable doctors across the UK and Europe predict who is at risk of having a heart attack or stroke in the next 10 years with greater accuracy. The calculator has been adopted by the European Guidelines on Cardiovascular Disease Prevention in Clinical Practice.
Developing imaging and artificial intelligence tools to improve diagnosis of heart and vascular disease by enhancing analysis of scans for disease activity and high-risk fatty plaques. These tools can be rapidly implemented to support diagnosis, treatment and prevention.
A study investigating whether an epilepsy medication could help to prevent strokes in people with a common gene variant. The change in the gene HDAC9 can cause it to become ‘overactive’ and increase stroke risk. The epilepsy medication sodium valproate blocks the HDAC9 activity, so could reduce stroke risk in people with the variant.
Discovery of rare and common changes in the genetic code that influences proteins and small molecules in the blood, helping us understand the development of cardiovascular diseases and identify novel drug targets.

Adapted from a press release by BHF

The University of Cambridge has received £5 million funding from the British Heart Foundation (BHF) to support its world-class cardiovascular disease research over the next five years, the charity has announced.

This is a fantastic achievement from the whole Cambridge team. This award will support our multiple research programmes.Martin BennettLloyd MannProfessor Martin Bennett standing outside the Victor Phillip Dahdaleh Heart and Lung Research Institute

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US Food and Drug Administration approves Cambridge-developed artificial pancreas

Fri, 24/05/2024 - 13:39

This means that even more people living with the disease will be able to use this life-changing app. For the first time, the FDA authorised the use of the artificial pancreas system in pregnancy.

CamAPS FX, produced by Cambridge spinout company CamDiab (www.camdiab.com), is an Android app that can be used to help manage glucose levels in people with type 1 diabetes, including during pregnancy.

The app allows a compatible insulin pump and a compatible continuous glucose monitor to ‘talk to each other’, creating an artificial pancreas.

The CamAPS FX closed loop algorithm was given FDA authorisation on Thursday 23 May. It had already been CE-marked for use in the UK and the EU.

CamAPS FX creator Roman Hovorka is Professor of Metabolic Technology at the Institute of Metabolic Science and Department of Paediatrics at the University of Cambridge, where the technology was developed.

He said: "We set out to help people with type 1 diabetes and their families live better lives and we’re delighted that the FDA has reviewed the safety and effectiveness of CamAPS FX and has given the technology its approval."

"It has been extensively tested and we’re proud that it is considered by many to be the best algorithm out there."

CamAPS FX is already used by more than 27,000 people in 15 countries across Europe and Australia. Artificial pancreas systems such as CamAPS FX have been granted approval for wide use by the NHS in November 2023 by the National Institute for Health and Care Excellence (NICE).

Imperceptible sensors made from ‘electronic spider silk’ can be printed directly on human skin

Fri, 24/05/2024 - 10:23

The method, developed by researchers from the University of Cambridge, takes its inspiration from spider silk, which can conform and stick to a range of surfaces. These ‘spider silks’ also incorporate bioelectronics, so that different sensing capabilities can be added to the ‘web’.

The fibres, at least 50 times smaller than a human hair, are so lightweight that the researchers printed them directly onto the fluffy seedhead of a dandelion without collapsing its structure. When printed on human skin, the fibre sensors conform to the skin and expose the sweat pores, so the wearer doesn’t detect their presence. Tests of the fibres printed onto a human finger suggest they could be used as continuous health monitors.

This low-waste and low-emission method for augmenting living structures could be used in a range of fields, from healthcare and virtual reality, to electronic textiles and environmental monitoring. The results are reported in the journal Nature Electronics.

Although human skin is remarkably sensitive, augmenting it with electronic sensors could fundamentally change how we interact with the world around us. For example, sensors printed directly onto the skin could be used for continuous health monitoring, for understanding skin sensations, or could improve the sensation of ‘reality’ in gaming or virtual reality application.

While wearable technologies with embedded sensors, such as smartwatches, are widely available, these devices can be uncomfortable, obtrusive and can inhibit the skin’s intrinsic sensations.

“If you want to accurately sense anything on a biological surface like skin or a leaf, the interface between the device and the surface is vital,” said Professor Yan Yan Shery Huang from Cambridge’s Department of Engineering, who led the research. “We also want bioelectronics that are completely imperceptible to the user, so they don’t in any way interfere with how the user interacts with the world, and we want them to be sustainable and low waste.”

There are multiple methods for making wearable sensors, but these all have drawbacks. Flexible electronics, for example, are normally printed on plastic films that don’t allow gas or moisture to pass through, so it would be like wrapping your skin in cling film. Other researchers have recently developed flexible electronics that are gas-permeable, like artificial skins, but these still interfere with normal sensation, and rely on energy- and waste-intensive manufacturing techniques.

3D printing is another potential route for bioelectronics since it is less wasteful than other production methods, but leads to thicker devices that can interfere with normal behaviour. Spinning electronic fibres results in devices that are imperceptible to the user, but don't have a high degree of sensitivity or sophistication, and they’re difficult to transfer onto the object in question.

Now, the Cambridge-led team has developed a new way of making high-performance bioelectronics that can be customised to a wide range of biological surfaces, from a fingertip to the fluffy seedhead of a dandelion, by printing them directly onto that surface. Their technique takes its inspiration in part from spiders, who create sophisticated and strong web structures adapted to their environment, using minimal material.

The researchers spun their bioelectronic ‘spider silk’ from PEDOT:PSS (a biocompatible conducting polymer), hyaluronic acid and polyethylene oxide. The high-performance fibres were produced from water-based solution at room temperature, which enabled the researchers to control the ‘spinnability’ of the fibres. The researchers then designed an orbital spinning approach to allow the fibres to morph to living surfaces, even down to microstructures such as fingerprints.

Tests of the bioelectronic fibres, on surfaces including human fingers and dandelion seedheads, showed that they provided high-quality sensor performance while being imperceptible to the host.

“Our spinning approach allows the bioelectronic fibres to follow the anatomy of different shapes, at both the micro and macro scale, without the need for any image recognition,” said Andy Wang, the first author of the paper. “It opens up a whole different angle in terms of how sustainable electronics and sensors can be made. It’s a much easier way to produce large area sensors.”

Most high-resolution sensors are made in an industrial cleanroom and require the use of toxic chemicals in a multi-step and energy-intensive fabrication process. The Cambridge-developed sensors can be made anywhere and use a tiny fraction of the energy that regular sensors require.

The bioelectronic fibres, which are repairable, can be simply washed away when they have reached the end of their useful lifetime, and generate less than a single milligram of waste: by comparison, a typical single load of laundry produces between 600 and 1500 milligrams of fibre waste.

“Using our simple fabrication technique, we can put sensors almost anywhere and repair them where and when they need it, without needing a big printing machine or a centralised manufacturing facility,” said Huang. “These sensors can be made on-demand, right where they’re needed, and produce minimal waste and emissions.”

The researchers say their devices could be used in applications from health monitoring and virtual reality, to precision agriculture and environmental monitoring. In future, other functional materials could be incorporated into this fibre printing method, to build integrated fibre sensors for augmenting the living systems with display, computation, and energy conversion functions. The research is being commercialised with the support of Cambridge Enterprise, the University’s commercialisation arm.

The research was supported in part by the European Research Council, Wellcome, the Royal Society, and the Biotechnology and Biological Sciences Research Council (BBSRC), part of UK Research and Innovation (UKRI).

Reference:
Wenyu Wang et al. ‘Sustainable and imperceptible augmentation of living structures with organic bioelectronic fibres.’ Nature Electronics (2024). DOI: 10.1038/s41928-024-01174-4

Researchers have developed a method to make adaptive and eco-friendly sensors that can be directly and imperceptibly printed onto a wide range of biological surfaces, whether that’s a finger or a flower petal.

Huang Lab, CambridgeSensors printed on human fingers

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One in two children with ADHD experience emotional problems, study finds

Wed, 22/05/2024 - 09:00

In research published in Nature Mental Health, the team found that as many as one in two children with ADHD show signs of emotional dysregulation, and that Ritalin – the commonly-prescribed drug to help the condition – appears to be less effective at treating this symptom.

ADHD affects around one in 14 young people under the age of 18 and in around half of these cases it persists into adulthood. The condition causes problems including hyperactivity, impulsivity and a difficulty to focus attention.

It has become increasingly clear that some people with ADHD also have self-control problems, affecting their ability to regulate emotions. For example, one in 50 (2.1%) children with a diagnosis of ADHD also have a mood disorder, such as depression, while more than one in four (27.4%) have an anxiety disorder. Many also have verbal or physical outbursts due to an inability to regulate their emotions.

These problems were thought to be a result of other symptoms associated with ADHD, such as problems with cognition and motivation. But today’s study shows that emotional dysregulation occurs independently of these.

The researchers examined data from the ABCD Study, a large longitudinal cohort that tracks the brain development and mental health of children from across the United States. Data on ADHD symptoms was available for just over 6,000 of these children, allowing the researchers to attribute a score to each individual indicating their likelihood of having ADHD.

A team of scientists from Fudan University in Shanghai, China, and the University of Cambridge identified 350 individuals within the cohort who had high symptom scores that met the clinical cut-off for ADHD. Two-thirds (65.7%) of these were male.

Parents or guardians of the children and adolescents in the cohort had previously completed a series of questionnaires, which included questions that related to emotional behaviour, for example:

When my child is upset, he/she has difficulty controlling his/her behaviours.

When my child is upset, he/she knows that he/she can find a way to eventually feel better.

When my child is upset, he/she starts to feel very bad about him/herself.

The researchers found that half (51.4%) of the individuals in the high-symptom group showed signs of emotion dysregulation and this was independent of cognitive and motivational problems.

Among children with only low-ADHD symptoms at both ages 12 and 13 years, those with a high scores of emotion dysregulation at age 13 years were 2.85 times more likely to have developed high-ADHD symptoms by age 14 years compared with those with a low score of emotion dysregulation.

When the researchers examined brain imaging data available for some of the participants, they discovered a particular region of the brain known as the pars orbitalis that was smaller among children who scored highly for ADHD and emotional problems. The pars orbitalis is at the front of the brain and plays an important role in understanding and processing of emotion and communication as well as inhibitory control over behaviour, which may explain some of the behaviours seen in ADHD.

Professor Barbara Sahakian from the Department of Psychiatry at the University of Cambridge and a Fellow of Clare Hall said: “The pars orbitalis is a well-connected part of the brain, and if it hasn’t developed properly it might make it difficult for individuals to control their emotions and communicate with others appropriately, especially in social situations.

“Parents and teachers often say they have problems controlling children with ADHD, and it could be that when the children can’t express themselves well – when they hit emotional difficulties – they may not be able to control their emotions and have an outburst rather than communicating with the parent, teacher or the other child.”

Professor Sahakian hopes that acknowledging emotion dysregulation as a key part of ADHD will help people better understand the problems the child is experiencing. This could lead to using effective treatments for regulation of emotion, such as cognitive behavioural therapy.

The findings may also point to potential ways to help the child manage their emotions, for example by using cognitive behavioural techniques to learn to stop and think before they react and to express their feelings verbally, or use techniques such as exercise or relaxation to calm themselves or alleviate symptoms of depression and anxiety.

This may be particularly important as the researchers found that Ritalin, the drug used to help manage ADHD symptoms, does not appear to fully treat symptoms of emotion dysregulation. Identifying the problem earlier would allow for alternative, more effective interventions to help the child better manage their emotions, potentially helping the individual in adulthood.

Professor Qiang Luo from Fudan University and a Life Member at Clare Hall, Cambridge, said: “If you're having trouble controlling your emotions, this can lead to problems with social interactions, which further exacerbates any depression or anxiety that you might have. It also might mean that you're saying things or doing things that exacerbate a situation rather than calming it down. Teaching vulnerable individuals from an early age how to manage your emotions and express yourself could help them overcome such problems further down the line.”

While it is not clear exactly what causes these problems in the first place, the researchers found signs of a link to possible dysfunction of the immune system, with individuals who exhibited signs of emotion dysregulation showing higher percentages of certain types of immune cell.

Professor Sahakian added: “We already know that problems with the immune system can be linked to depression, and we’ve seen similar patterns in individuals with ADHD who experience emotion dysregulation.”

The research was supported by the National Key Research and Development Program of China, the National Natural Science Foundation of China, the Program of Shanghai Academic Research Leader and the Shanghai Municipal Science and Technology Major Project.

Reference
Hou, W et al. Emotion dysregulation and right pars orbitalis constitute a neuropsychological pathway to attention deficit hyperactivity disorder. Nature Mental Health; 13 May 2024: DOI: 10.1038/s44220-024-00251-z

Cambridge scientists have shown that problems regulating emotions – which can manifest as depression, anxiety and explosive outbursts – may be a core symptom of attention deficit hyperactivity disorder (ADHD).

When the children can’t express themselves well – when they hit emotional difficulties – they may not be able to control their emotions and have an outburst rather than communicatingBarbara SahakianConstantinis (Getty Images)Teenage boys fighting on way to school

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More than 1,000 may have died in Nazi camps on island of Alderney, report finds

Wed, 22/05/2024 - 07:51

A review of evidence, gathered by a panel of 13 international experts, including Cambridge archaeologist Dr Gilly Carr, has sought to give the most accurate possible assessment of how many prisoners and labourers died on the Channel Island between 1941 to 1945.

During this time, crimes were committed against forced and slave labourers, transported from countries across Europe and brought to Alderney to construct fortifications as part of the German war effort. Housed in camps that shared many of the traits of those in mainland Europe, these labourers were subject to atrocious living and working conditions, and, in some cases, executions. 

Commissioned by Lord Eric Pickles, UK Special Envoy on Post Holocaust Issues, the investigation aims to dispel conspiracy theories and provide the most accurate figure possible of those who lost their lives on the island. The report also aims to bring justice for those who died, and ensure that this period of history, and the Holocaust, is remembered fully and accurately.

The team’s calculation of the minimum number of prisoners or labourers sent to Alderney throughout the German occupation stands between 7,608 and 7,812 people. Death figures calculated after Alderney was liberated by the British originally suggested that 389 people died as a result of ill-treatment. Now, the Alderney Expert Review Panel has found that the number of deaths in Alderney is likely to range between 641 and 1,027.

The review panel has concluded that there is no evidence that many thousands of victims died, and that claims Alderney constituted a ‘mini-Auschwitz’ are unsubstantiated.

Dr Carr, Associate Professor in Archaeology at Cambridge’s Institute of Continuing Education, and Fellow of St Catharine’s College, who co-ordinated the panel, said: “I am proud of the way the team of experts came together to provide answers to the questions set by Lord Pickles. It shows what can be achieved when you bring together the right people with the right experience and expertise who are committed to working in memory of those who suffered in Alderney during the Occupation.”

Chief Rabbi Sir Ephraim Mirvis KBE said: “The findings of the Alderney Review are a significant and welcome development. Having an authoritative account of this harrowing element of the island’s history is vital. It enables us to accurately remember the individuals who so tragically suffered and died on British soil. Marking the relevant sites will now be an appropriate step to take, to ensure that this information is widely available.”

The panel also sought to discover why German perpetrators were not tried by Britain for war crimes committed in Alderney. It concluded that a war crimes investigation carried out in Alderney immediately after the war was “wholly serious in intent”. But because most of the victims were Soviet citizens, the case was handed to the Russians. In exchange, Germans who murdered British servicemen in Stalag Luft III during the “Great Escape” were handed over to Britain.

The report says the Soviet Union did not follow up the Alderney case and were thus responsible for the failure to bring the perpetrators to justice, causing much anger among members of the British government.

The number of people killed during the Nazi Occupation of Alderney is far greater than the figure previously thought, according to a new report published today, which says more than 1,000 could have perished.

[The report] shows what can be achieved when you bring together the right people with the right experience and expertise who are committed to working in memory of those who suffered in Alderney during the OccupationDr Gilly Carr, Institute of Continuing Education"Nazi Fire Control Tower on Alderney" by neilalderney123 is licensed under CC BY-NC 2.0.

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Cambridge experts awarded 2024 Academy of Medical Sciences Fellowships

Tue, 21/05/2024 - 00:01

Professor Nita Forouhi from the Medical Research Council (MRC) Epidemiology Unit and Professor Susan Gathercole from the MRC Cognition and Brain Sciences Unit join an esteemed Fellowship of over 1,400 researchers who have been recognised for their remarkable contributions to advancing biomedical and health sciences, ground-breaking research discoveries and translating developments into benefits for patients and wider society.

Professor Nita Forouhi is a clinical scientist whose research is focused on the link between diet, nutrition and the risk of diabetes, obesity and related disorders. She is Professor of Population Health and Nutrition and leads the Nutritional Epidemiology programme, which was awarded the Vice-Chancellor’s Best Impact Award in 2016. She frequently engages with the media to promote knowledge in the area of diet and health.

Professor Susan Gathercole is a cognitive psychologist with interests in memory and learning, including the causes of specific learning difficulties in children and how they might be overcome. Susan became a Fellow of the British Academy in 2014 and was awarded an OBE for services to psychology and education in 2016.

Professor Andrew Morris PMedSci, President of the Academy of Medical Sciences, said: “It is an honour to welcome these brilliant minds to our Fellowship. Our new Fellows lead pioneering work in biomedical research and are driving remarkable improvements in healthcare. We look forward to working with them, and learning from them, in our quest to foster an open and progressive research environment that improves the health of people everywhere through excellence in medical science.

“It is also welcoming to note that this year's cohort is our most diverse yet, in terms of gender, ethnicity and geography. While this progress is encouraging, we recognise that there is still much work to be done to truly diversify our Fellowship. We remain committed to our EDI goals and will continue to take meaningful steps to ensure our Fellowship reflects the rich diversity of the society we serve."

The new Fellows will be formally admitted to the Academy at a ceremony on Wednesday 18 September 2024.

Two Cambridge Fellows are among the new Academy of Medical Sciences Fellows announced today.

Academy of Medical Sciences Academy of Medical Sciences logo

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“I feel like I’m Alice in Wonderland”: nightmares and ‘daymares’ could be early warning signs of autoimmune disease

Mon, 20/05/2024 - 23:30

The researchers argue that there needs to be greater recognition that these types of mental health and neurological symptoms can act as an early warning sign that an individual is approaching a ‘flare’, where their disease worsens for a period.

In a study published today in eClinicalMedicine, researchers surveyed 676 people living with lupus and 400 clinicians, as well as carrying out detailed interviews with 69 people living with systemic autoimmune rheumatic diseases (including lupus) and 50 clinicians. Lupus is an autoimmune inflammatory disease known for its effect on many organs including the brain.

In the study, the team also asked patients about the timing of 29 neurological and mental health symptoms (such as depression, hallucinations and loss of balance). In interviews, patients were also asked if they could list the order that symptoms usually occurred when their disease was flaring.

One of the more common symptoms reported was disrupted dream sleep, experienced by three in five patients, a third of whom reported this symptom appearing over a year before onset of lupus disease.

Just under one in four patients reported hallucinations, though for 85% of these the symptom did not appear until around the onset of disease or later. When the researchers interviewed the patients, however, they found that three in five lupus patients and one in three with other rheumatology-related conditions reported increasingly disrupted dreaming sleep – usually vivid and distressing nightmares – just before their hallucinations. These nightmares were often vivid and distressing, involving being attacked, trapped, crushed, or falling.

One patient from Ireland described their nightmares as: “Horrific, like murders, like skin coming off people, horrific…I think it’s like when I’m overwhelmed which could be the lupus being bad…So I think the more stress my body is under then the more vivid and bad the dreaming would be.”

The study interviewers found that using the term ‘daymares’ to talk about hallucinations often led to a ‘lightbulb’ moment for patients, and they felt that it was a less frightening and stigmatised word.

A patient from England said: “[When] you said that word daymare and as soon as you said that it just made sense, it’s like not necessarily scary, it’s just like you’ve had a dream and yet you’re sitting awake in the garden…I see different things, it’s like I come out of it and it’s like when you wake up and you can’t remember your dream and you’re there but you’re not there… it’s like feeling really disorientated, the nearest thing I can think of is that I feel like I’m Alice in Wonderland.”

Patients experiencing hallucinations were reluctant to share their experiences, and many specialists said they had never considered nightmares and hallucinations as being related to disease flares. Most said they would talk to their patients about nightmares and hallucinations in future, agreeing that recognising these early flare symptoms may provide an ‘early warning system’ enabling them to improve care and even reduce clinic times by averting flares at any earlier stage.

Lead author Dr Melanie Sloan from the Department of Public Health and Primary Care at the University of Cambridge said: “It’s important that clinicians talk to their patients about these types of symptoms and spend time writing down each patient’s individual progression of symptoms. Patients often know which symptoms are a bad sign that their disease is about to flare, but both patients and doctors can be reluctant to discuss mental health and neurological symptoms, particularly if they don’t realise that these can be a part of autoimmune diseases.”

Senior study author Professor David D’Cruz from Kings College London said: “For many years, I have discussed nightmares with my lupus patients and thought that there was a link with their disease activity. This research provides evidence of this, and we are strongly encouraging more doctors to ask about nightmares and other neuropsychiatric symptoms – thought to be unusual, but actually very common in systemic autoimmunity – to help us detect disease flares earlier.”

The importance of recognising these symptoms was highlighted by reports that some patients had initially been misdiagnosed or even hospitalised with a psychotic episode and/or suicidal ideation, which was only later found to be the first sign of their autoimmune disease.

One patient from Scotland said: “At 18 I was diagnosed with borderline personality disorder, and then 6 months later with lupus at 19, so it’s all very close together and it was strange that when my [borderline personality disorder] got under control and my lupus got under control was within 6 months.”

A nurse from Scotland said: “I’ve seen them admitted for an episode of psychosis and the lupus isn’t screened for until someone says ‘oh I wonder if it might be lupus’...but it was several months and very difficult… especially with young women and it’s learning more that that is how lupus affects some people and it’s not anti-psychotic drugs they needed, it’s like a lot of steroids.”

Professor Guy Leschziner, a study author and neurologist at Guys’ and St Thomas’ hospital, and author of The Secret World of Sleep, said: "We have long been aware that alterations in dreaming may signify changes in physical, neurological and mental health, and can sometimes be early indicators of disease. However, this is the first evidence that nightmares may also help us monitor such a serious autoimmune condition like lupus, and is an important prompt to patients and clinicians alike that sleep symptoms may tell us about impending relapse."

The research was funded by The Lupus Trust and is part of the INSPIRE project (Investigating Neuropsychiatric Symptom Prevalence and Impact in Rheumatology patient Experiences).

Reference
Sloan, M. et al. Neuropsychiatric prodromes and symptom timings in relation to disease onset and/or flares in SLE: results from the mixed methods international INSPIRE study. eClinicalMedicine; 21 May 2024; DOI: 10.1016/j.eclinm.2024.102634

An increase in nightmares and hallucinations – or ‘daymares’ – could herald the onset of autoimmune diseases such as lupus, say an international team led by researchers at the University of Cambridge and King’s College London.

Both patients and doctors can be reluctant to discuss mental health and neurological symptoms, particularly if they don’t realise that these can be a part of autoimmune diseasesMel SloanDavid Wall (Getty Images)A ghostly figure silhouetted between trees in a forest

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Winners of Vice-Chancellor’s Social Impact Awards 2024 announced

Mon, 20/05/2024 - 16:04

The awards, organised by Cambridge Hub and sponsored by the Vice Chancellor’s Office, recognise and celebrate exceptional achievement in contributing to society. University of Cambridge Vice-Chancellor Professor Deborah Prentice hosted the ceremony on 30 April, which saw 15 students recognised with awards.

Undergraduate Student Awards

Sakshi Jha from Clare College

Sakshi is a law finalist, who co-founded Cambridge Freedom from Torture, a refugee-aid group, where she formed part of the first student volunteering convoy to Calais, France. Sakshi is also leading a policy paper examining UK asylum policy; she is on the Managing Board of the Cambridge Human Rights Law Journal, and she is the founding Co-Editor in Chief of the Clare College Law Journal, where she interviewed Supreme Court Justices on prevalent legal issues such as human rights and international law enforcement. Sakshi has also aided fundraising efforts as Treasurer of Cambridge Amnesty International, and is a legal researcher for a social consulting firm, completing commissioned research for the United Nations High Commissioner for Refugees.

Millie May from St John's College

Millie is a third-year politics and social anthropology undergraduate at St John's College. She is extremely passionate about climate and social justice-related work and has been the Lead of the Cambridge Climate Society Education Team for two academic years. She has led several projects in this role, the main being a campaign and student-faculty collaborative effort to integrate climate-related content across degrees at Cambridge, which she presented at COP28 to advocate for an integrated climate change curriculum on an international level.

Faustine Petron from Department of Sociology

Faustine is a final-year Human, Social and Political Sciences student specialising in Sociology. She is interested in gendered violence and feminist modes of resistance in the Maghreb and South Asia. Outside of academia, Faustine is an award-winning campaigner who works with the government and charities in using education as a tool to prevent gendered violence in the UK.

Josephine Somerville from Clare College

Jo is a third-year English student who has acted on her passion for making long-lasting positive changes for biodiversity and climate change, centrally in the role of lead of the Cambridge Climate Society Action team. In 2023 she led the prosecution in the Generation on Trial project and more recently has initiated collaborations between the student bodies and the local community. The most extensive campaign she has been running is the Pesticide-Free Cambridge Colleges Campaign.

Master’s Student Award

Ming Hong Choi from Hughes Hall

Ming is a Master of Finance candidate at Cambridge Judge Business School, supported by both the UK Government’s Chevening Scholarship and Cambridge Trust Scholarship. He has made contributions across and beyond Cambridge through various leadership and advisory roles in youth leadership and development, real estate, investment, arts, sustainability, and educational initiatives.

PhD Student Awards

Samantha Hodder from Clare College

Sam is a final year PhD student studying cancer biology in the Department of Biochemistry. During a clinical placement early on in her PhD, Sam saw how important it is for children with cancer to be well informed about what they’ll be going through during the course of their treatment. This experience led Sam to begin the development of Chum, an app based learning and support platform for children with cancer and their families.

Swetha Kannan from Trinity Hall

Swetha is a PhD student at the Department of Medicine, as well as a successful junior scientist, educator, and social entrepreneur. Her key contributions to the local Cambridge community have been a result of her involvement with Make-A-Smile Cambridge, Student Minds Cambridge and the Cambridge Development Initiative. Swetha also established The Lalitha Foundation, a non-profit organisation in India dedicated to the betterment of lives of cancer- and post-sepsis patients.

Mine Koprulu from Pembroke College

Mine is a final year PhD student in Medical Sciences at MRC Epidemiology Unit. Improving the lives of others and making the world a better place to live in has been a long-standing aspiration of Mine’s. Professionally, she is aiming to improve healthcare by better understanding the biological basis of diseases and identifying effective treatment opportunities. In parallel, she also has been leading and contributing to various social impact projects, ranging from building more inclusive communities to promoting gender equity.

Nazifa Rafa from Lucy Cavendish College

Nazifa is a PhD student in Geography and a pioneering researcher dedicated to addressing pressing environmental and social justice issues. Her work spans biodiversity conservation, climate change, disaster risk, water and energy security, environmental health, and sustainable development, with a focus on empowering marginalised communities.

Mayumi Sato from Trinity Hall

Mayumi is a PhD student and Gates Cambridge Scholar, and the founder and director of SustainED. She has several years' experience working with climate-affected groups, predominantly in the Global South. Her academic and advocacy interests involve leading campaigns and initiatives for impact-based community development and justice-oriented research. Her interests focus on the intersection between social equity, environmental justice, and community engagement.

Volunteering Award

Kate Lucas from Homerton College

Kate is a third year undergraduate studying Manufacturing Engineering, who is dedicated to increasing diversity in engineering. As well as being President of Cambridge University Robotics Society and organising Unibots UK 2023 and 2024, she also mentors Year 13 students through platforms such as Zero Gravity and is also an active ambassador for Homerton Changemakers.

Innovation Award

William Lan from St Catharine's College

William is an MPhil student in Medical Science who has significantly contributed to mental health advocacy and community support. He is the Postgraduate Welfare Officer at St Catharine’s College, Vice-Chair of the International Students’ Campaign, and a Mental Health Foundation Young Leader, launching crucial welfare programmes and peer-support systems. William says his innovative methods and steadfast commitment to mental health advocacy have broadened his impact, establishing him as a force for positive change within and beyond the academic community.

Global Impact Award

Paulina Pérez-Duarte Mendiola from Sidney Sussex College

Paulina is a PhD candidate focusing on play and health at the Faculty of Education. She is a paediatrician, medical anthropologist and advocate for children’s holistic health and healthcare equity. Her work focuses on the role and impact of play in sick children’s development, learning and healthcare experiences. She is the Founder and Director of Semana JIM, which is the acronym of Play in Hospital Awareness Week in Mexico.

Impact in the Local Community Award

Zara Crapper from Robinson College

Zara is a third-year undergraduate in Natural Sciences. She has been involved in Scouting since she was young, and before her arrival in Cambridge she was an adult volunteer for a Cub Scout group in Andover. Since coming to Cambridge, she has opened a new section in a local Group, enabling the youngest members in the Scouting family from across the community to come together and learn in an enjoyable and inclusive environment.

Sustainability Award

Clara Ma from Selwyn College

Clara is a Gates Cambridge Scholar at Selwyn College, an alumna of Churchill College and a PhD student in environmental science and policy at the Cambridge Centre for Environment, Energy and Natural Resource Governance. She assists departments, colleges, and organisations across the University in transitioning to more sustainable food procurement.

The winners of this year’s Vice-Chancellor’s Social Impact Awards have been announced.

The winners of this year’s Vice-Chancellor’s Social Impact Awards

Yes

Earth’s earliest sea creatures drove evolution by stirring the water

Fri, 17/05/2024 - 16:01

A study involving the University of Cambridge has used virtual recreations of the earliest animal ecosystems, known as marine animal forests, to demonstrate the part they played in the evolution of our planet.

Using state-of-the-art computer simulations of fossils from the Ediacaran time period - approximately 565 million years ago - scientists discovered how these animals mixed the surrounding seawater. This may have affected the distribution of important resources such as food particles and could have increased local oxygen levels.

Through this process, the scientists think these early communities could have played a crucial role in shaping the initial emergence of large and complex organisms prior to a major evolutionary radiation of different forms of animal life, the so-called Cambrian ‘explosion’.

Over long periods of time, these changes might have allowed life forms to perform more complicated functions, like those associated with the evolution of new feeding and movement styles.

The study was led by the Natural History Museum and is published today in the journal Current Biology.

Dr Emily Mitchell at the University of Cambridge’s Department of Zoology, a co-author of the report, said: “It’s exciting to learn that the very first animals from 580 million years ago had a significant impact on their environment, despite not being able to move or swim. We’ve found they mixed up the water and enabled resources to spread more widely - potentially encouraging more evolution.”

Scientists know from modern marine environments that nutrients like food and oxygen are carried in seawater, and that animals can affect water flow in ways that influence the distribution of these resources.

To test how far back this process goes in Earth’s history, the team looked at some of the earliest examples of marine animal communities, known from rocks at Mistaken Point, Newfoundland, Canada. This world-famous fossil site perfectly preserves early life forms thanks to a cover of volcanic ash (sometimes referred to as an ‘Ediacaran Pompeii’).

Although some of these life forms look like plants, analysis of their anatomy and growth strongly suggests they are animals. Owing to the exceptional preservation of the fossils, the scientists could recreate digital models of key species, which were used as a basis for further computational analyses.

First author Dr Susana Gutarra, a Scientific Associate at the Natural History Museum, said: “We used ecological modelling and computer simulations to investigate how 3D virtual assemblages of Ediacaran life forms affected water flow. Our results showed that these communities were capable of ecological functions similar to those seen in present-day marine ecosystems.”

The study showed that one of the most important Ediacaran organisms for disrupting the flow of water was the cabbage-shaped animal Bradgatia, named after Bradgate Park in England. The Bradgatia from Mistaken Point are among some of the largest fossils known from this site, reaching diameters of over 50 centimetres.

Through their influence on the water around them, the scientists believe these Ediacaran organisms might have been capable of enhancing local oxygen concentrations. This biological mixing might also have had repercussions for the wider environment, possibly making other areas of the sea floor more habitable and perhaps even driving evolutionary innovation.

Dr Imran Rahman, lead author and Principal Researcher at the Natural History Museum, said: “The approach we’ve developed to study Ediacaran fossil communities is entirely new in palaeontology, providing us with a powerful tool for studying how past and present marine ecosystems might shape and influence their environment.”

The research was funded by the UK Natural Environment Research Council and the US National Science Foundation.

Reference: Gutarra-Diaz, S.“Ediacaran marine animal forests and the ventilation of the oceans.” May 2024, Current Biology. DOI: 10.1016/j.cub.2024.04.059

Adapted from a press release by the Natural History Museum

3D reconstructions suggest that simple marine animals living over 560 million years ago drove the emergence of more complex life by mixing the seawater around them

It’s exciting to learn that the very first animals from 580 million years ago had a significant impact on their environment, despite not being able to move or swim.Emily MitchellHugo Salais, Metazoa StudioArtistic recreation of the marine animal forest

YesLicence type: Attribution-Noncommerical

Webb detects most distant black hole merger to date

Thu, 16/05/2024 - 18:34

Astronomers have found supermassive black holes with masses of millions to billions times that of the Sun in most massive galaxies in the local Universe, including in our Milky Way galaxy. These black holes have likely had a major impact on the evolution of the galaxies they reside in. However, scientists still don’t fully understand how these objects grew to become so massive.

The finding of gargantuan black holes already in place in the first billion years after the Big Bang indicates that such growth must have happened very rapidly, and very early. Now, the James Webb Space Telescope is shedding new light on the growth of black holes in the early Universe.

The new Webb observations have provided evidence for an ongoing merger of two galaxies and their massive black holes when the Universe was just 740 million years old. The system is known as ZS7.

Massive black holes that are actively accreting matter have distinctive spectrographic features that allow astronomers to identify them. For very distant galaxies, like those in this study, these signatures are inaccessible from the ground and can only be seen with Webb.

“We found evidence for very dense gas with fast motions in the vicinity of the black hole, as well as hot and highly ionised gas illuminated by the energetic radiation typically produced by black holes in their accretion episodes,” said lead author Dr Hannah Übler of Cambridge’s Cavendish Laboratory and Kavli Institute for Cosmology. “Thanks to the unprecedented sharpness of its imaging capabilities, Webb also allowed our team to spatially separate the two black holes.”

The team found that one of the two black holes has a mass that is 50 million times the mass of the Sun. “The mass of the other black hole is likely similar, although it is much harder to measure because this second black hole is buried in dense gas,” said team member Professor Roberto Maiolino, also from the Kavli Institute.

“Our findings suggest that merging is an important route through which black holes can rapidly grow, even at cosmic dawn,” said Übler. “Together with other Webb findings of active, massive black holes in the distant Universe, our results also show that massive black holes have been shaping the evolution of galaxies from the very beginning.”

The team notes that once the two black holes merge, they will also generate gravitational waves. Events like this will be detectable with the next generation of gravitational wave observatories, such as the upcoming Laser Interferometer Space Antenna (LISA) mission, which was recently approved by the European Space Agency and will be the first space-based observatory dedicated to studying gravitational waves.

This discovery was from observations made as part of the Galaxy Assembly with NIRSpec Integral Field Spectroscopy programme. The team has recently been awarded a new Large Programme in Webb’s Cycle 3 of observations, to study in detail the relationship between massive black holes and their host galaxies in the first billion years. An important component of this programme will be to systematically search for and characterise black hole mergers. This effort will determine the rate at which black hole merging occurs at early cosmic epochs and will assess the role of merging in the early growth of black holes and the rate at which gravitational waves are produced from the dawn of time.

These results have been published in the Monthly Notices of the Royal Astronomical Society.

Reference:
Hannah Übler et al. ‘GA-NIFS: JWST discovers an offset AGN 740 million years after the big bang’ Monthly Notices of the Royal Astronomical Society (2024). DOI: 10.1093/mnras/stae943

Adapted from a press release by the European Space Agency.

An international team of astronomers, led by the University of Cambridge, has used the James Webb Space Telescope to find evidence for an ongoing merger of two galaxies and their massive black holes when the Universe was only 740 million years old. This marks the most distant detection of a black hole merger ever obtained and the first time that this phenomenon has been detected so early in the Universe.

Massive black holes have been shaping the evolution of galaxies from the very beginningHannah ÜblerESA/Webb, NASA, CSA, J. Dunlop, H. Übler, R. Maiolino, et. alThe environment of the galaxy system ZS7 from the JWST PRIMER programme as seen by Webb's NIRCam instrument

YesLicence type: Attribution

Nine Cambridge scientists elected as Fellows of the Royal Society 2024

Thu, 16/05/2024 - 09:51

The Royal Society is a self-governing Fellowship of many of the world’s most distinguished scientists drawn from all areas of science, engineering and medicine.

The Society’s fundamental purpose, as it has been since its foundation in 1660, is to recognise, promote and support excellence in science and to encourage the development and use of science for the benefit of humanity.

This year, over 90 researchers, innovators and communicators from around the world have been elected as Fellows of the Royal Society for their substantial contribution to the advancement of science. Nine of these are from the University of Cambridge.

Sir Adrian Smith, President of the Royal Society said: “I am pleased to welcome such an outstanding group into the Fellowship of the Royal Society.

“This new cohort have already made significant contributions to our understanding of the world around us and continue to push the boundaries of possibility in academic research and industry.

“From visualising the sharp rise in global temperatures since the industrial revolution to leading the response to the Covid-19 pandemic, their diverse range of expertise is furthering human understanding and helping to address some of our greatest challenges. It is an honour to have them join the Fellowship.”

The Fellows and Foreign Members join the ranks of Stephen Hawking, Isaac Newton, Charles Darwin, Albert Einstein, Lise Meitner, Subrahmanyan Chandrasekhar and Dorothy Hodgkin.

The new Cambridge fellows are:

Professor Sir John Aston Kt FRS

Aston is the Harding Professor of Statistics in Public Life at the Statistical Laboratory, Department of Pure Mathematics and Mathematical Statistics, where he develops techniques for public policy and improves the use of quantitative methods in public policy debates.

From 2017 to 2020 he was the Chief Scientific Adviser to the Home Office, providing statistical and scientific advice to ministers and officials, and was involved in the UK’s response to the Covid pandemic. He was knighted in 2021 for services to statistics and public policymaking, and is a Fellow of Churchill College.

Professor Sarah-Jayne Blakemore FBA FMedSci FRS

Blakemore is the Professor of Psychology and Cognitive Neuroscience, Department of Psychology, and leader of the Developmental Cognitive Neuroscience Group. Her research focuses on the development of social cognition and decision making in the human adolescent brain, and adolescent mental health.

Blakemore has been awarded several national and international prizes for her research, and is a Fellow of the British Academy, the American Association of Psychological Science and the Academy of Medical Sciences.

Professor Patrick Chinnery FMedSci FRS

Chinnery is Professor of Neurology and head of the University’s Department of Clinical Neurosciences, and a Fellow of Gonville & Caius College. He was appointed Executive Chair of the Medical Research Council last year, having previously been MRC Clinical Director since 2019.

His principal research is the role of mitochondria in human disease and developing new treatments for mitochondrial disorders. Chinnery is a Wellcome Principal Research Fellow with a lab based in the MRC Mitochondrial Biology Unit and jointly chairs the NIHR BioResource for Translational Research in Common and Rare Diseases. He is a Fellow of the Academy of Medical Sciences.

Professor Rebecca Fitzgerald FMedSci FRS

Fitzgerald is Professor of Cancer Prevention in the Department of Oncology and the inaugural Director of the University’s new Early Cancer Institute, which launched in 2022. She is a Fellow of Trinity College.

Her pioneering work to devise a first-in-class, non-endoscopic capsule sponge test for identifying individuals at high risk for oesophageal cancer has won numerous prizes, including the Westminster Medal, and this test is now being rolled out in the NHS and beyond by her spin-out Cyted Ltd.

Professor David Hodell FRS

Hodell is the Woodwardian Professor of Geology and Director of the Godwin Laboratory for Palaeoclimate Research in the Department of Earth Sciences, and a Fellow of Clare College.

A marine geologist and paleoclimatologist, his research focuses on high-resolution paleoclimate records from marine and lake sediments, as well as mineral deposits, to better understand past climate dynamics. Hodell is a fellow of the American Geophysical Union and the American Association for the Advancement of Science. He has received the Milutin Milankovic Medal.

Professor Eric Lauga FRS

Lauga is Professor of Applied Mathematics in the Department of Applied Mathematics and Theoretical Physics, where his research is in fluid mechanics, biophysics and soft matter. Lauga is the author, or co-author, of over 180 publications and currently serves as Associate Editor for the journal Physical Review Fluids.

He is a recipient of three awards from the American Physical Society: the Andreas Acrivos Dissertation Award in Fluid Dynamics, the François Frenkiel Award for Fluid Mechanics and the Early Career Award for Soft Matter Research. He is a Fellow of the American Physical Society and of Trinity College.

Professor George Malliaras FRS

Malliaras is the Prince Philip Professor of Technology in the Department of Engineering, where he leads a group that works on the development and translation of implantable and wearable devices that interface with electrically active tissues, with applications in neurological disorders and brain cancer.

Research conducted by Malliaras has received awards from the European Academy of Sciences, the New York Academy of Sciences, and the US National Science Foundation among others. He is a Fellow of the Materials Research Society and of the Royal Society of Chemistry.

Professor Oscar Randal-Williams FRS

Randal-Williams is the Sadleirian Professor of Pure Mathematics in the Department of Pure Mathematics and Mathematical Statistics.

He has received the Whitehead Prize from the London Mathematical Society, a Philip Leverhulme Prize, the Oberwolfach Prize, the Dannie Heineman Prize of the Göttingen Academy of Sciences and Humanities, and was jointly awarded the Clay Research Award.

Randal-Williams is one of two managing editors of the Proceedings of the London Mathematical Society, and an editor of the Journal of Topology.

Professor Mihaela van der Schaar FRS

Van der Schaar is the John Humphrey Plummer Professor of Machine Learning, Artificial Intelligence and Medicine in the Departments of Applied Mathematics and Theoretical Physics, Engineering and Medicine.

She is the founder and director of the Cambridge Centre for AI in Medicine, and a Fellow at The Alan Turing Institute. Her work has received numerous awards, including the Oon Prize on Preventative Medicine, a National Science Foundation CAREER Award, and the IEEE Darlington Award.

Van der Schaar is credited as inventor on 35 US patents, and has made over 45 contributions to international standards for which she received three ISO Awards. In 2019, a Nesta report declared her the most-cited female AI researcher in the UK.

Nine outstanding Cambridge researchers have been elected as Fellows of the Royal Society, the UK’s national academy of sciences and the oldest science academy in continuous existence.

Royal SocietyThe Royal Society in central London

Yes

2023 was the hottest summer in two thousand years

Tue, 14/05/2024 - 16:00

Although 2023 has been reported as the hottest year on record, the instrumental evidence only reaches back as far as 1850 at best, and most records are limited to certain regions.

Now, by using past climate information from annually resolved tree rings over two millennia, scientists from the University of Cambridge and the Johannes Gutenberg University Mainz have shown how exceptional the summer of 2023 was.

Even allowing for natural climate variations over hundreds of years, 2023 was still the hottest summer since the height of the Roman Empire, exceeding the extremes of natural climate variability by half a degree Celsius.

“When you look at the long sweep of history, you can see just how dramatic recent global warming is,” said co-author Professor Ulf Büntgen, from Cambridge’s Department of Geography. “2023 was an exceptionally hot year, and this trend will continue unless we reduce greenhouse gas emissions dramatically.”

The results, reported in the journal Nature, also demonstrate that in the Northern Hemisphere, the 2015 Paris Agreement to limit warming to 1.5C above pre-industrial levels has already been breached.

Early instrumental temperature records, from 1850-1900, are sparse and inconsistent. The researchers compared early instrumental data with a large-scale tree ring dataset and found the 19th century temperature baseline used to contextualise global warming is several tenths of a degree Celsius colder than previously thought. By re-calibrating this baseline, the researchers calculated that summer 2023 conditions in the Northern Hemisphere were 2.07C warmer than mean summer temperatures between 1850 and 1900.

“Many of the conversations we have around global warming are tied to a baseline temperature from the mid-19th century, but why is this the baseline? What is normal, in the context of a constantly-changing climate, when we’ve only got 150 years of meteorological measurements?” said Büntgen. “Only when we look at climate reconstructions can we better account for natural variability and put recent anthropogenic climate change into context.”

Tree rings can provide that context, since they contain annually-resolved and absolutely-dated information about past summer temperatures. Using tree-ring chronologies allows researchers to look much further back in time without the uncertainty associated with some early instrumental measurements.

The available tree-ring data reveals that most of the cooler periods over the past 2000 years, such as the Little Antique Ice Age in the 6th century and the Little Ice Age in the early 19th century, followed large-sulphur-rich volcanic eruptions. These eruptions spew huge amounts of aerosols into the stratosphere, triggering rapid surface cooling. The coldest summer of the past two thousand years, in 536 CE, followed one such eruption, and was 3.93C colder than the summer of 2023.

Most of the warmer periods covered by the tree ring data can be attributed to the El Niño climate pattern, or El Niño-Southern Oscillation (ENSO). El Niño affects weather worldwide due to weakened trade winds in the Pacific Ocean and often results in warmer summers in the Northern Hemisphere. While El Niño events were first noted by fisherman in the 17th century, they can be observed in the tree ring data much further back in time.

However, over the past 60 years, global warming caused by greenhouse gas emissions are causing El Niño events to become stronger, resulting in hotter summers. The current El Niño event is expected to continue into early summer 2024, making it likely that this summer will break temperature records once again.

“It’s true that the climate is always changing, but the warming in 2023, caused by greenhouse gases, is additionally amplified by El Niño conditions, so we end up with longer and more severe heat waves and extended periods of drought,” said Professor Jan Esper, the lead author of the study from the Johannes Gutenberg University Mainz in Germany. “When you look at the big picture, it shows just how urgent it is that we reduce greenhouse gas emissions immediately.”

The researchers note that while their results are robust for the Northern Hemisphere, it is difficult to obtain global averages for the same period since data is sparse for the Southern Hemisphere. The Southern Hemisphere also responds differently to climate change, since it is far more ocean-covered than the Northern Hemisphere.

The research was supported in part by the European Research Council.

Reference:
Jan Esper, Max Torbenson, Ulf Büntgen. ‘2023 summer warmth unparalleled over the past 2,000 years.’ Nature (2024). DOI: 10.1038/s41586-024-07512-y

Researchers have found that 2023 was the hottest summer in the Northern Hemisphere in the past two thousand years, almost four degrees warmer than the coldest summer during the same period.

When you look at the long sweep of history, you can see just how dramatic recent global warming isUlf Büntgentrekandshoot via Getty ImagesMorning sun over Los Angeles

Yes

Over 20,000 people join search for new dementia treatments

Tue, 14/05/2024 - 10:00

Using the resource, scientists have already been able to show for the first time that two important bodily mechanisms – inflammation and metabolism – play a role in the decline in brain function as we age.

By 2050, approximately 139 million people are expected to be living with dementia worldwide. In the UK, in 2022, UK Prime Minister launched the Dame Barbara Windsor Dementia Mission, part of the government’s commitment to double increase research funding for dementia.

Although there has been recent progress developing drugs that slow down progression of the disease, the two leading treatments only have a small effect, and the vast majority of new approaches that work in animal studies fail when it comes to patient clinical trials.

One explanation for these failures is that the drugs are tested in people who already have memory loss – and by this point, it may be too late to stop or reverse the disease. Hence, there is an urgent need to understand what is going on before people develop symptoms at the very early stages of disease, and to test new treatments before people come to their doctor with cognitive problems. This approach requires a large cohort of participants willing to be recalled for clinical and experimental studies of cognitive decline.

Today, writing in the journal Nature Medicine, scientists led by the University of Cambridge in partnership with the Alzheimer’s Society report how they have recruited 21,000 people aged 17-85 to the Genes and Cognition Cohort within the National Institute for Health and Care Research (NIHR) BioResource.

The NIHR BioResource was established in 2007 to recruit volunteers keen to engage in experimental medicine and clinical trials across the whole of medicine. Approximately half of its participants are recruited to disease specific cohorts, but the other half are from the general public, and detailed information about their genetics and their physical makeup has been collected. They have all given their consent to be contacted about future research studies.

For the Genes and Cognition Cohort, researchers used a combination of cognitive tests and genetic data, combined with other health data and demographic information, to enable the first at-scale study of cognitive changes. This will allow the team to recruit participants for studies of cognitive decline and new treatments for this.

For example, a pharmaceutical company with a promising new drug candidate to slow the cognitive decline could recruit people through the BioResource based on their profile and invite them to join in the clinical trial. Having a baseline measurement for their cognitive performance will allow scientists to observe whether the drug slows their expected cognitive decline.

Professor Patrick Chinnery from the Department of Clinical Neurosciences at the University of Cambridge and co-Chair of the NIHR BioResource, who has led the project, said: “We’ve created a resource that is unmatched anywhere else in the world, recruiting people who are not showing any signs of dementia rather than people already having symptoms. It will allow us to match individuals to particular studies and speed up the development of much-needed new drugs to treat dementia.

“We know that over time our cognitive function decreases, so we’ve plotted out the expected trajectory of various different cognitive functions over our volunteers’ life course according to their genetic risk. We’ve also asked the question, ‘What are the genetic mechanisms that predispose you to slow or fast cognitive decline as you age?’.”

Using the research, the team have identified two mechanisms that appear to affect cognition as we age and could serve as potential targets to slow down cognitive decline and thereby delay the onset of dementia. The first of these is inflammation, with immune cells specific to the brain and central nervous system – known as microglia – causing gradual deterioration of the brain and hence its ability to perform key cognitive functions. The second mechanism relates to metabolism – in particular, how carbohydrates are broken down in the brain to release energy.

Professor Chinnery added: “Cognitive decline is a natural process, but when it drops below a particular threshold, that’s when there’s a problem – that is when we would diagnose dementia. Anything that slows that decline will delay when we drop below that threshold. If you could put off the onset of dementia from 65 to 75 or even 85, it would make a huge difference at an individual and at a population level.”

Dr Richard Oakley, Associate Director of Research and Innovation at Alzheimer’s Society, said: “This exciting study, funded by Alzheimer’s Society, is an important step in helping us to better understand how the diseases that cause dementia begin, and will aid in the development of new treatments that target the early stages of these diseases.

“The data, from over 20,000 volunteers, helps us to better understand the connection between participants’ genes and cognitive decline and allows for further ground-breaking analysis in future.

“One in three people born in the UK today will go on to develop dementia in their lifetime but research will beat dementia. We need to make it a reality sooner through more funding, partnership working and people taking part in dementia research.”

For further information about how you can join the BioResource and contribute to studies like this one and many others, please visit www.bioresource.nihr.ac.uk.

The research was carried out in collaboration with the Medical Research Council Biostatistics Unit and was supported by the Alzheimer’s Society and the NIHR BioResource. The researchers were also supported by Wellcome and the Medical Research Council.

Reference
Rahman, MS et al. Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition Cohort participants. Nat Med; 14 May 2024; DOI: 10.1038/s41591-024-02960-5

More than 20,000 volunteers have been recruited to a resource aimed at speeding up the development of much-needed dementia drugs. The cohort will enable scientists in universities and industry to involve healthy individuals who may be at increased risk of dementia in clinical trials to test whether new drugs can slow the decline in various brain functions including memory and delay the onset of dementia.

We’ve created a resource that is unmatched anywhere else in the world, recruiting people who are not showing any signs of dementia rather than people already having symptomsPatrick ChinneryHalfpoint Images (Getty Images)Smiling elderly woman speaking to a healthcare worker

Yes

Birth by C-section more than doubles odds of measles vaccine failure

Mon, 13/05/2024 - 10:01

A study by the University of Cambridge, UK, and Fudan University, China, has found that a single dose of the measles jab is up to 2.6 times more likely to be completely ineffective in children born by C-section, compared to those born naturally.

Failure of the vaccine means that the child’s immune system does not produce antibodies to fight against measles infection, so they remain susceptible to the disease.

A second measles jab was found to induce a robust immunity against measles in C-section children.

Measles is a highly infectious disease, and even low vaccine failure rates can significantly increase the risk of an outbreak.

A potential reason for this effect is linked to the development of the infant’s gut microbiome – the vast collection of microbes that naturally live inside the gut. Other studies have shown that vaginal birth transfers a greater variety of microbes from mother to baby, which can boost the immune system.

“We’ve discovered that the way we’re born - either by C-section or natural birth - has long-term consequences on our immunity to diseases as we grow up,” said Professor Henrik Salje in the University of Cambridge’s Department of Genetics, joint senior author of the report.

He added: “We know that a lot of children don't end up having their second measles jab, which is dangerous for them as individuals and for the wider population.

“Infants born by C-section are the ones we really want to be following up to make sure they get their second measles jab, because their first jab is much more likely to fail.”

The results are published today in the journal Nature Microbiology.

At least 95% of the population needs to be fully vaccinated to keep measles under control but the UK is well below this, despite the Measles, Mumps and Rubella (MMR) vaccine being available through the NHS Routine Childhood Immunisation Programme.

An increasing number of women around the world are choosing to give birth by caesarean section: in the UK a third of all births are by C-section, in Brazil and Turkey over half of all children are born this way.

“With a C-section birth, children aren’t exposed to the mother’s microbiome in the same way as with a vaginal birth. We think this means they take longer to catch up in developing their gut microbiome, and with it, the ability of the immune system to be primed by vaccines against diseases including measles,” said Salje.

To get their results, the researchers used data from previous studies of over 1,500 children in Hunan, China, which included blood samples taken every few weeks from birth to the age of 12. This allowed them to see how levels of measles antibodies in the blood change over the first few years of life, including following vaccination.

They found that 12% of children born via caesarean section had no immune response to their first measles vaccination, as compared to 5% of children born by vaginal delivery. This means that many of the children born by C-section did still mount an immune response following their first vaccination.

Two doses of the measles jab are needed for the body to mount a long-lasting immune response and protect against measles. According to the World Health Organisation, in 2022 only 83% of the world's children had received one dose of measles vaccine by their first birthday – the lowest since 2008.

Salje said: “Vaccine hesitancy is really problematic, and measles is top of the list of diseases we’re worried about because it’s so infectious.”

Measles is one of the world’s most contagious diseases, spread by coughs and sneezes. It starts with cold-like symptoms and a rash, and can lead to serious complications including blindness, seizures, and death.

Before the measles vaccine was introduced in 1963, there were major measles epidemics every few years causing an estimated 2.6 million deaths each year.

The research was funded by the National Natural Science Foundation of China.

Reference

Wang, W. et al: ‘Dynamics of measles immunity from birth and following vaccination.’ Nature Microbiology, 13 May 2024. DOI: 10.1038/s41564-024-01694-x

Researchers say it is vital that children born by caesarean section receive two doses of the measles vaccine for robust protection against the disease.

CHBD / E+ / Getty Images Very sick 5 year old little boy fighting measles infection, boy is laying in bed under the blanket with a agonizing expression, boy is covered with rash caused by virus.

Yes

Baby born deaf can hear after breakthrough gene therapy

Thu, 09/05/2024 - 08:32

Opal Sandy from Oxfordshire is the first patient treated in a global gene therapy trial, which shows “mind-blowing” results. She is the first British patient in the world and the youngest child to receive this type of treatment.

Opal was born completely deaf because of a rare genetic condition, auditory neuropathy, caused by the disruption of nerve impulses travelling from the inner ear to the brain.

Within four weeks of having the gene therapy infusion to her right ear, Opal responded to sound, even with the cochlear implant in her left ear switched off.

Clinicians noticed continuous improvement in Opal’s hearing in the weeks afterwards. At 24 weeks, they confirmed Opal had close to normal hearing levels for soft sounds, such as whispering, in her treated ear.

Now 18 months old, Opal can respond to her parents’ voices and can communicate words such as “Dada” and “bye-bye.”

Opal’s mother, Jo Sandy, said: “When Opal could first hear us clapping unaided it was mind-blowing - we were so happy when the clinical team confirmed at 24 weeks that her hearing was also picking up softer sounds and speech. The phrase ‘near normal’ hearing was used and everyone was so excited such amazing results had been achieved.”

Auditory neuropathy can be due to a variation in a single gene, known as the OTOF gene. The gene produces a protein called otoferlin, needed to allow the inner hair cells in the ear to communicate with the hearing nerve. Approximately 20,000 people across the UK, Germany, France, Spain, Italy and UK and are deaf due to a mutation in the OTOF gene.

The CHORD trial, which started in May 2023, aims to show whether gene therapy can provide hearing for children born with auditory neuropathy.

Professor Manohar Bance from the Department of Clinical Neurosciences at the University of Cambridge and an ear surgeon at Cambridge University Hospitals NHS Foundation Trust is chief investigator of the trial. He said:

“These results are spectacular and better than I expected. Gene therapy has been the future of otology and audiology for many years and I’m so excited that it is now finally here. This is hopefully the start of a new era for gene therapies for the inner ear and many types of hearing loss.”

Children with a variation in the OTOF gene often pass the newborn screening, as the hair cells are working, but they are not talking to the nerve. It means this hearing loss is not commonly detected until children are 2 or 3 years of age – when a delay in speech is likely to be noticed.

Professor Bance added: “We have a short time frame to intervene because of the rapid pace of brain development at this age. Delays in the diagnosis can also cause confusion for families as the many reasons for delayed speech and late intervention can impact a children’s development.”

“More than sixty years after the cochlear implant was first invented – the standard of care treatment for patients with OTOF related hearing loss – this trial shows gene therapy could provide a future alternative. It marks a new era in the treatment for deafness. It also supports the development of other gene therapies that may prove to make a difference in other genetic related hearing conditions, many of which are more common than auditory neuropathy.”

Mutations in the OTOF gene can be identified by standard NHS genetic testing. Opal was identified as being at risk as her older sister has the condition; this was confirmed by genetic test result when she was 3 weeks old.

Opal was given an infusion containing a harmless virus (AAV1). It delivers a working copy of the OTOF gene and is delivered via an injection in the cochlea during surgery under general anaesthesia. During surgery, while Opal was given the gene therapy in right ear, a cochlear implant was fitted in her left ear.

James Sandy, Opal’s father said: “It was our ultimate goal for Opal to hear all the speech sounds. It’s already making a difference to our day-to-day lives, like at bath-time or swimming, when Opal can’t wear her cochlear implant. We feel so proud to have contributed to such pivotal findings, which will hopefully help other children like Opal and their families in the future.”

Opal’s 24-week results, alongside other scientific data from the CHORD trial are being presented at the American Society of Gene and Cell Therapy (ASGC) in Baltimore, USA this week.

Dr Richard Brown, Consultant Paediatrician at CUH, who is an Investigator on the CHORD trial, said: “The development of genomic medicine and alternative treatments is vital for patients worldwide, and increasingly offers hope to children with previously incurable disorders. It is likely that in the long run such treatments require less follow up so may prove to be an attractive option, including within the developing world. Follow up appointments have shown effective results so far with no adverse reactions and it is exciting to see the results to date.

“Within the new planned Cambridge Children’s Hospital, we look forward to having a genomic centre of excellence which will support patients from across the region to access the testing they need, and the best treatment, at the right time.”

The CHORD trial has been funded by Regeneron. Patients are being enrolled in the study in the US, UK and Spain.

Patients in the first phase of the study receive a low dose to one ear. The second phase are expected to use a higher dose of gene therapy in one ear only, following proven safety of the starting dose. The third phase will look at gene therapy in both ears with the dose selected after ensuring the safety and effectiveness in parts 1 and 2. Follow up appointments will continue for five years for enrolled patients, which will show how patients adapt to understand speech in the longer term.

In Cambridge, the trial is supported by NIHR Cambridge Clinical Research Facility and NIHR Cambridge Biomedical Research Centre.

Adapted from a press release from CUH

A baby girl born deaf can hear unaided for the first time, after receiving gene therapy when she was eleven months old at Addenbrooke’s Hospital in Cambridge.

Gene therapy has been the future of otology and audiology for many years and I’m so excited that it is now finally hereManohar BanceCambridge University Hospitals NHS Foundation TrustBaby Opal and mother Jo

Yes

Call for safeguards to prevent unwanted ‘hauntings’ by AI chatbots of dead loved ones

Thu, 09/05/2024 - 08:06

Artificial intelligence that allows users to hold text and voice conversations with lost loved ones runs the risk of causing psychological harm and even digitally “haunting” those left behind without design safety standards, according to University of Cambridge researchers.

‘Deadbots’ or ‘Griefbots’ are AI chatbots that simulate the language patterns and personality traits of the dead using the digital footprints they leave behind. Some companies are already offering these services, providing an entirely new type of “postmortem presence”.

AI ethicists from Cambridge’s Leverhulme Centre for the Future of Intelligence outline three design scenarios for platforms that could emerge as part of the developing “digital afterlife industry”, to show the potential consequences of careless design in an area of AI they describe as “high risk”.

The research, published in the journal Philosophy and Technology, highlights the potential for companies to use deadbots to surreptitiously advertise products to users in the manner of a departed loved one, or distress children by insisting a dead parent is still “with you”.

When the living sign up to be virtually re-created after they die, resulting chatbots could be used by companies to spam surviving family and friends with unsolicited notifications, reminders and updates about the services they provide – akin to being digitally “stalked by the dead”.

Even those who take initial comfort from a ‘deadbot’ may get drained by daily interactions that become an “overwhelming emotional weight”, argue researchers, yet may also be powerless to have an AI simulation suspended if their now-deceased loved one signed a lengthy contract with a digital afterlife service.

“Rapid advancements in generative AI mean that nearly anyone with Internet access and some basic know-how can revive a deceased loved one,” said Dr Katarzyna Nowaczyk-Basińska, study co-author and researcher at Cambridge’s Leverhulme Centre for the Future of Intelligence (LCFI).

“This area of AI is an ethical minefield. It’s important to prioritise the dignity of the deceased, and ensure that this isn’t encroached on by financial motives of digital afterlife services, for example.

“At the same time, a person may leave an AI simulation as a farewell gift for loved ones who are not prepared to process their grief in this manner. The rights of both data donors and those who interact with AI afterlife services should be equally safeguarded.”

Platforms offering to recreate the dead with AI for a small fee already exist, such as ‘Project December’, which started out harnessing GPT models before developing its own systems, and apps including ‘HereAfter’. Similar services have also begun to emerge in China.

One of the potential scenarios in the new paper is “MaNana”: a conversational AI service allowing people to create a deadbot simulating their deceased grandmother without consent of the “data donor” (the dead grandparent).

The hypothetical scenario sees an adult grandchild who is initially impressed and comforted by the technology start to receive advertisements once a “premium trial” finishes. For example, the chatbot suggesting ordering from food delivery services in the voice and style of the deceased.

The relative feels they have disrespected the memory of their grandmother, and wishes to have the deadbot turned off, but in a meaningful way – something the service providers haven’t considered.

“People might develop strong emotional bonds with such simulations, which will make them particularly vulnerable to manipulation,” said co-author Dr Tomasz Hollanek, also from Cambridge’s LCFI.

“Methods and even rituals for retiring deadbots in a dignified way should be considered. This may mean a form of digital funeral, for example, or other types of ceremony depending on the social context.”

“We recommend design protocols that prevent deadbots being utilised in disrespectful ways, such as for advertising or having an active presence on social media.”

While Hollanek and Nowaczyk-Basińska say that designers of re-creation services should actively seek consent from data donors before they pass, they argue that a ban on deadbots based on non-consenting donors would be unfeasible.

They suggest that design processes should involve a series of prompts for those looking to “resurrect” their loved ones, such as ‘have you ever spoken with X about how they would like to be remembered?’, so the dignity of the departed is foregrounded in deadbot development.

Another scenario featured in the paper, an imagined company called “Paren’t”, highlights the example of a terminally ill woman leaving a deadbot to assist her eight-year-old son with the grieving process.

While the deadbot initially helps as a therapeutic aid, the AI starts to generate confusing responses as it adapts to the needs of the child, such as depicting an impending in-person encounter.

The researchers recommend age restrictions for deadbots, and also call for “meaningful transparency” to ensure users are consistently aware that they are interacting with an AI. These could be similar to current warnings on content that may cause seizures, for example.

The final scenario explored by the study – a fictional company called “Stay” – shows an older person secretly committing to a deadbot of themselves and paying for a twenty-year subscription, in the hopes it will comfort their adult children and allow their grandchildren to know them.

After death, the service kicks in. One adult child does not engage, and receives a barrage of emails in the voice of their dead parent. Another does, but ends up emotionally exhausted and wracked with guilt over the fate of the deadbot. Yet suspending the deadbot would violate the terms of the contract their parent signed with the service company.

“It is vital that digital afterlife services consider the rights and consent not just of those they recreate, but those who will have to interact with the simulations,” said Hollanek.

“These services run the risk of causing huge distress to people if they are subjected to unwanted digital hauntings from alarmingly accurate AI recreations of those they have lost. The potential psychological effect, particularly at an already difficult time, could be devastating.”

The researchers call for design teams to prioritise opt-out protocols that allow potential users terminate their relationships with deadbots in ways that provide emotional closure.

Added Nowaczyk-Basińska: “We need to start thinking now about how we mitigate the social and psychological risks of digital immortality, because the technology is already here.”

Cambridge researchers lay out the need for design safety protocols that prevent the emerging “digital afterlife industry” causing social and psychological harm.

Tomasz HollanekA visualisation of one of the design scenarios highlighted in the latest paper

Yes

‘Wraparound’ implants represent new approach to treating spinal cord injuries

Wed, 08/05/2024 - 19:01

A team of engineers, neuroscientists and surgeons from the University of Cambridge developed the devices and used them to record the nerve signals going back and forth between the brain and the spinal cord. Unlike current approaches, the Cambridge devices can record 360-degree information, giving a complete picture of spinal cord activity.

Tests in live animal and human cadaver models showed the devices could also stimulate limb movement and bypass complete spinal cord injuries where communication between the brain and spinal cord had been completely interrupted.

Most current approaches to treating spinal injuries involve both piercing the spinal cord with electrodes and placing implants in the brain, which are both high-risk surgeries. The Cambridge-developed devices could lead to treatments for spinal injuries without the need for brain surgery, which would be far safer for patients.

While such treatments are still at least several years away, the researchers say the devices could be useful in the near-term for monitoring spinal cord activity during surgery. Better understanding of the spinal cord, which is difficult to study, could lead to improved treatments for a range of conditions, including chronic pain, inflammation and hypertension. The results are reported in the journal Science Advances.

“The spinal cord is like a highway, carrying information in the form of nerve impulses to and from the brain,” said Professor George Malliaras from the Department of Engineering, who co-led the research. “Damage to the spinal cord causes that traffic to be interrupted, resulting in profound disability, including irreversible loss of sensory and motor functions.”

The ability to monitor signals going to and from the spinal cord could dramatically aid in the development of treatments for spinal injuries, and could also be useful in the nearer term for better monitoring of the spinal cord during surgery.

“Most technologies for monitoring or stimulating the spinal cord only interact with motor neurons along the back, or dorsal, part of the spinal cord,” said Dr Damiano Barone from the Department of Clinical Neurosciences, who co-led the research. “These approaches can only reach between 20 and 30 percent of the spine, so you’re getting an incomplete picture.”

By taking their inspiration from microelectronics, the researchers developed a way to gain information from the whole spine, by wrapping very thin, high-resolution implants around the spinal cord’s circumference. This is the first time that safe 360-degree recording of the spinal cord has been possible – earlier approaches for 360-degree monitoring use electrodes that pierce the spine, which can cause spinal injury.

The Cambridge-developed biocompatible devices – just a few millionths of a metre thick – are made using advanced photolithography and thin film deposition techniques, and require minimal power to function.

The devices intercept the signals travelling on the axons, or nerve fibres, of the spinal cord, allowing the signals to be recorded. The thinness of the devices means they can record the signals without causing any damage to the nerves, since they do not penetrate the spinal cord itself.

“It was a difficult process, because we haven’t made spinal implants in this way before, and it wasn’t clear that we could safely and successfully place them around the spine,” said Malliaras. “But because of recent advances in both engineering and neurosurgery, the planets have aligned and we’ve made major progress in this important area.”

The devices were implanted using an adaptation to routine surgical procedure so they could be slid under the spinal cord without damaging it. In tests using rat models, the researchers successfully used the devices to stimulate limb movement. The devices showed very low latency – that is, their reaction time was close to human reflexive movement. Further tests in human cadaver models showed that the devices can be successfully placed in humans.

The researchers say their approach could change how spinal injuries are treated in future. Current attempts to treat spinal injuries involve both brain and spinal implants, but the Cambridge researchers say the brain implants may not be necessary.

“If someone has a spinal injury, their brain is fine, but it’s the connection that’s been interrupted,” said Barone. “As a surgeon, you want to go where the problem is, so adding brain surgery on top of spinal surgery just increases the risk to the patient. We can collect all the information we need from the spinal cord in a far less invasive way, so this would be a much safer approach for treating spinal injuries.”

While a treatment for spinal injuries is still years away, in the nearer term, the devices could be useful for researchers and surgeons to learn more about this vital, but understudied, part of human anatomy in a non-invasive way. The Cambridge researchers are currently planning to use the devices to monitor nerve activity in the spinal cord during surgery.

“It’s been almost impossible to study the whole of the spinal cord directly in a human, because it’s so delicate and complex,” said Barone. “Monitoring during surgery will help us to understand the spinal cord better without damaging it, which in turn will help us develop better therapies for conditions like chronic pain, hypertension or inflammation. This approach shows enormous potential for helping patients.”

The research was supported in part by the Royal College of Surgeons, the Academy of Medical Sciences, Health Education England, the National Institute for Health Research, and the Engineering and Physical Sciences Research Council (EPSRC), part of UK Research and Innovation (UKRI).

Reference:
Ben J Woodington, Jiang Lei et al. ‘Flexible Circumferential Bioelectronics to Enable 360-degree Recording and Stimulation of the Spinal Cord.’ Science Advances (2024). DOI: 10.1126/sciadv.adl1230

A tiny, flexible electronic device that wraps around the spinal cord could represent a new approach to the treatment of spinal injuries, which can cause profound disability and paralysis.

Because of recent advances in both engineering and neurosurgery, the planets have aligned and we’ve made major progress in this important areaGeorge MalliarasSEBASTIAN KAULITZKI/SCIENCE PHOTO LIBRARYIllustration of spinal cord

Yes

New vaccine effective against coronaviruses that haven’t even emerged yet

Mon, 06/05/2024 - 10:00

This is a new approach to vaccine development called ‘proactive vaccinology’, where scientists build a vaccine before the disease-causing pathogen even emerges.

The new vaccine works by training the body’s immune system to recognise specific regions of eight different coronaviruses, including SARS-CoV-1, SARS-CoV-2, and several that are currently circulating in bats and have potential to jump to humans and cause a pandemic.

Key to its effectiveness is that the specific virus regions the vaccine targets also appear in many related coronaviruses. By training the immune system to attack these regions, it gives protection against other coronaviruses not represented in the vaccine – including ones that haven’t even been identified yet.

For example, the new vaccine does not include the SARS-CoV-1 coronavirus, which caused the 2003 SARS outbreak, yet it still induces an immune response to that virus.

“Our focus is to create a vaccine that will protect us against the next coronavirus pandemic, and have it ready before the pandemic has even started,” said Rory Hills, a graduate researcher in the University of Cambridge’s Department of Pharmacology and first author of the report.

He added: “We’ve created a vaccine that provides protection against a broad range of different coronaviruses – including ones we don’t even know about yet.”

The results are published today in the journal Nature Nanotechnology.

“We don’t have to wait for new coronaviruses to emerge. We know enough about coronaviruses, and different immune responses to them, that we can get going with building protective vaccines against unknown coronaviruses now,” said Professor Mark Howarth in the University of Cambridge’s Department of Pharmacology, senior author of the report.

He added: “Scientists did a great job in quickly producing an extremely effective COVID vaccine during the last pandemic, but the world still had a massive crisis with a huge number of deaths. We need to work out how we can do even better than that in the future, and a powerful component of that is starting to build the vaccines in advance.”

The new ‘Quartet Nanocage’ vaccine is based on a structure called a nanoparticle – a ball of proteins held together by incredibly strong interactions. Chains of different viral antigens are attached to this nanoparticle using a novel ‘protein superglue’. Multiple antigens are included in these chains, which trains the immune system to target specific regions shared across a broad range of coronaviruses.

This study demonstrated that the new vaccine raises a broad immune response, even in mice that were pre-immunised with SARS-CoV-2.

The new vaccine is much simpler in design than other broadly protective vaccines currently in development, which the researchers say should accelerate its route into clinical trials.

The underlying technology they have developed also has potential for use in vaccine development to protect against many other health challenges.

The work involved a collaboration between scientists at the University of Cambridge, the University of Oxford, and Caltech. It improves on previous work, by the Oxford and Caltech groups, to develop a novel all-in-one vaccine against coronavirus threats. The vaccine developed by Oxford and Caltech should enter Phase 1 clinical trials in early 2025, but its complex nature makes it challenging to manufacture which could limit large-scale production.

Conventional vaccines include a single antigen to train the immune system to target a single specific virus. This may not protect against a diverse range of existing coronaviruses, or against pathogens that are newly emerging.

The research was funded by the Biotechnology and Biological Sciences Research Council.

Reference: Hills, R.A. et al: ‘Proactive vaccination using multiviral Quartet Nanocages to elicit broad anti-coronavirus responses.’ Nature Nanotechnology, May 2024. DOI: 10.1038/s41565-024-01655-9

Researchers have developed a new vaccine technology that has been shown in mice to provide protection against a broad range of coronaviruses with potential for future disease outbreaks - including ones we don’t even know about

Our focus is to create a vaccine that will protect us against the next coronavirus pandemic, and have it ready before the pandemic has even started.Rory HillsStefan Cristian Cioata on GettySyringe and vaccine bottle

YesLicence type: Attribution-Noncommerical

Ice shelves fracture under weight of meltwater lakes

Fri, 03/05/2024 - 15:31

When air temperatures in Antarctica rise and glacier ice melts, water can pool on the surface of floating ice shelves, weighing them down and causing the ice to bend. Now, for the first time in the field, researchers have shown that ice shelves don’t just buckle under the weight of meltwater lakes — they fracture.

As the climate warms and melt rates in Antarctica increase, this fracturing could cause vulnerable ice shelves to collapse, allowing inland glacier ice to spill into the ocean and contribute to sea level rise.

Ice shelves are important for the Antarctic Ice Sheet’s overall health as they act to buttress or hold back the glacier ice on land. Scientists have predicted and modelled that surface meltwater loading could cause ice shelves to fracture, but no one had observed the process in the field, until now.

The new study, published in the Journal of Glaciology, may help explain how the Larsen B Ice Shelf abruptly collapsed in 2002. In the months before its catastrophic breakup, thousands of meltwater lakes littered the ice shelf’s surface, which then drained over just a few weeks.

To investigate the impacts of surface meltwater on ice shelf stability, a research team led by the University of Colorado Boulder, and including researchers from the University of Cambridge, travelled to the George VI Ice Shelf on the Antarctic Peninsula in November 2019.

First, the team identified a depression or ‘doline’ in the ice surface that had formed by a previous lake drainage event where they thought meltwater was likely to pool again on the ice. Then, they ventured out on snowmobiles, pulling all their science equipment and safety gear behind on sleds.

Around the doline, the team installed high-precision GPS stations to measure small changes in elevation at the ice’s surface, water-pressure sensors to measure lake depth, and a timelapse camera system to capture images of the ice surface and meltwater lakes every 30 minutes.

In 2020, the COVID-19 pandemic brought their fieldwork to a screeching halt. When the team finally made it back to their field site in November 2021, only two GPS sensors and one timelapse camera remained; two other GPS and all water pressure sensors had been flooded and buried in solid ice. Fortunately, the surviving instruments captured the vertical and horizontal movement of the ice’s surface and images of the meltwater lake that formed and drained during the record-high 2019/2020 melt season.

GPS data indicated that the ice in the centre of the lake basin flexed downward about a foot in response to the increased weight from meltwater. That finding builds upon previous work that produced the first direct field measurements of ice shelf buckling caused by meltwater ponding and drainage.

The team also found that the horizontal distance between the edge and centre of the meltwater lake basin increased by over a foot. This was most likely due to the formation and/or widening of circular fractures around the meltwater lake, which the timelapse imagery captured. Their results provide the first field-based evidence of ice shelf fracturing in response to a surface meltwater lake weighing down the ice.

“This is an exciting discovery,” said lead author Alison Banwell, from the Cooperative Institute for Research in Environmental Sciences (CIRES) at the University of Colorado Boulder. “We believe these types of circular fractures were key in the chain reaction style lake drainage process that helped to break up the Larsen B Ice Shelf.”

“While these measurements were made over a small area, they demonstrate that bending and breaking of floating ice due to surface water may be more widespread than previously thought,” said co-author Dr Rebecca Dell from Cambridge’s Scott Polar Research Institute. “As melting increases in response to predicted warming, ice shelves may become more prone to break up and collapse than they are currently.”

“This has implications for sea level as the buttressing of inland ice is reduced or removed, allowing the glaciers and ice streams to flow more rapidly into the ocean,” said co-author Professor Ian Willis, also from SPRI.

The work supports modelling results that show the immense weight of thousands of meltwater lakes and subsequent draining caused the Larsen B Ice Shelf to bend and break, contributing to its collapse.

“These observations are important because they can be used to improve models to better predict which Antarctic ice shelves are more vulnerable and most susceptible to collapse in the future,” Banwell said.

The research was funded by the U.S. National Science Foundation (NSF) and the Natural Environment Research Council (NERC), part of UK Research and Innovation (UKRI). The team also included researchers from the University of Oxford and the University of Chicago. Rebecca Dell is a Fellow of Trinity Hall, Cambridge.

Reference:
Alison F Banwell et al. ‘Observed meltwater-induced flexure and fracture at a doline on George VI Ice Shelf, Antarctica.’ Journal of Glaciology (2024). DOI: 10.1017/jog.2024.31

Adapted from a CIRES press release.

Heavy pooling meltwater can fracture ice, potentially leading to ice shelf collapse

Ian WillisAli Banwell and Laura Stevens installing the time-lapse camera used in this study on the George VI Ice Shelf in Antarctica.

Yes

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