They were given infected blood products in trials without their knowledge, the BBC has found.
Octopus inspires new suction mechanism for robots

A new robotic suction cup which can grasp rough, curved and heavy stone, has been developed by scientists at the University of Bristol.
The team, based at Bristol Robotics Laboratory, studied the structures of octopus biological suckers, which have superb adaptive suction abilities enabling them to anchor to rock.
In their findings, published in the journal PNAS today, the researchers show how they were able create a multi-layer soft structure and an artificial fluidic system to mimic the musculature and mucus structures of biological suckers.
Suction is a highly evolved biological adhesion strategy for soft-body organisms to achieve strong grasping on various objects. Biological suckers can adaptively attach to dry complex surfaces such as rocks and shells, which are extremely challenging for current artificial suction cups. Although the adaptive suction of biological suckers is believed to be the result of their soft body’s mechanical deformation, some studies imply that in-sucker mucus secretion may be another critical factor in helping attach to complex surfaces, thanks to its high viscosity.
Lead author Tianqi Yue explained: “The most important development is that we successfully demonstrated the effectiveness of the combination of mechanical conformation — the use of soft materials to conform to surface shape, and liquid seal — the spread of water onto the contacting surface for improving the suction adaptability on complex surfaces. This may also be the secret behind biological organisms ability to achieve adaptive suction.”
Their multi-scale suction mechanism is an organic combination of mechanical conformation and regulated water seal. Multi-layer soft materials first generate a rough mechanical conformation to the substrate, reducing leaking apertures to just micrometres. The remaining micron-sized apertures are then sealed by regulated water secretion from an artificial fluidic system based on the physical model, thereby the suction cup achieves long suction longevity on diverse surfaces but with minimal overflow.
Tianqi added: “We believe the presented multi-scale adaptive suction mechanism is a powerful new adaptive suction strategy which may be instrumental in the development of versatile soft adhesion.
“Current industrial solutions use always-on air pumps to actively generate the suction however, these are noisy and waste energy.
“With no need for a pump, it is well known that many natural organisms with suckers, including octopuses, some fishes such as suckerfish and remoras, leeches, gastropods and echinoderms, can maintain their superb adaptive suction on complex surfaces by exploiting their soft body structures.”
The findings have great potential for industrial applications, such as providing a next-generation robotic gripper for grasping a variety of irregular objects.
The team now plan to build a more intelligent suction cup, by embedding sensors into the suction cup to regulate suction cup’s behaviour.
Siblings with unique genetic change help scientists progress drug search for type 1 diabetes

Two siblings who have the only known mutations in a key gene anywhere in the world have helped scientists gain new insights that could help progress the search for new treatments in type 1 diabetes.
Type 1 diabetes (also known as autoimmune diabetes) is a devastating and life-long disease, in which the patient’s immune cells wrongly destroy the insulin producing beta cells in the pancreas. People living with autoimmune diabetes need to test their blood sugar and inject insulin throughout their lives to control their blood sugars and prevent complications.
Autoimmune diabetes with clinical onset in very early childhood is rare and can result from a variety of genetic variants. However, there are many cases of early onset diabetes without known genetic explanation. In addition, some cancer patients treated with a category of immunotherapy known as immune checkpoint inhibitors — which target the same pathway that the mutation was found in — are prone to developing autoimmune diabetes. The reason why only this category of cancer immunotherapy can trigger autoimmune diabetes is not well understood. Like type 1 diabetes, genetic or immunotherapy-associated autoimmune diabetes requires life-long insulin replacement therapy — there is currently no cure.
The new research, published in the Journal of Experimental Medicine, began when researchers studied two siblings who were diagnosed with a rare genetic form of autoimmune diabetes in the first weeks of life. The University of Exeter offers free genetic testing worldwide for babies diagnosed with diabetes before they are nine months old. For most of these babies, this service provides a genetic diagnosis and in around half of these babies, it allows for a change in treatment.
When researchers tested the two siblings in the study, no mutation in any of the known causes was identified. The Exeter team then performed whole genome sequencing to look for previously unknown causes of autoimmune diabetes. Through this sequencing, they found a mutation in the gene encoding PD-L1 in the siblings and realised it could be responsible for their very-early-onset autoimmune diabetes.
Study authorDr Matthew Johnson, from the University of Exeter, UK, said: “PD-L1 has been particularly well studied in animal models because of its crucial function in sending a stop signal to the immune system and its relevance to cancer immunotherapy. But, to our knowledge, nobody has ever found humans with a disease-causing mutation in the gene encoding PD-L1. We searched the globe, looking at all the large-scale datasets that we know of, and we haven’t been able to find another family. These siblings therefore provide us with a unique and incredibly important opportunity to investigate what happens when this gene is disabled in humans.”
The PD-L1 protein is expressed on many different cell types. Its receptor, PD-1, is expressed exclusively on immune cells. When the two proteins bind together it provides a stop signal to the immune system, preventing collateral damage to the bodies tissues and organs.
Researchers from the Rockefeller Institute in New York and King’s College London joined forces with Exeter to study the siblings, with funding from Wellcome, The Leona M. and Harry B. Helmsley Charitable Trust, Diabetes UK, and the US National Institutes for Health. After contacting the family’s clinician in Morocco, the Exeter team visited the siblings where they were living to collect samples and return them to King’s College London, within the crucial ten-hour window for analysis while the immune cells were still alive. The London and New York teams then performed extensive analysis on the siblings’ cells.
Study co-author Dr Masato Ogishi, from the Rockefeller University in New York, said: “We first showed that the mutation completely disabled the function of PD-L1 protein. We then studied the immune system of the siblings to look for immunological abnormalities that could account for their extremely early-onset diabetes. As we previously described another two siblings with PD-1 deficiency, both of whom had multi-organ autoimmunity including autoimmune diabetes and extensive dysregulation in their immune cells, we expected to find severe dysregulation of the immune system in the PD-L1-deficient siblings. To our great surprise, their immune systems looked pretty much normal in almost all aspects throughout the study. Therefore, PD-L1 is certainly indispensable for preventing autoimmune diabetes but is dispensable for many other aspects of human immune system. We think that PD-L2, another ligand of PD-1, albeit less well-studied than PD-L1, may be serving as a back-up system when PD-L1 is not available. This concept needs to be further investigated in the context of artificial blockade for PD-L1 as cancer immunotherapy.”
Study co-author Professor Timothy Tree, from King’s College London, said: “Through studying this one set of siblings — unique in the world to our knowledge — we have found that the PD-L1 gene is essential for avoiding autoimmune diabetes, but is not essential for ‘everyday’ immune function. This leads us to the grand question; ‘what is the role of PD-L1 in our pancreas making it critical for preventing our immune cells destroying our beta cells?’ We know that under certain conditions beta cells express PD-L1. However, certain types of immune cells in the pancreas also express PD-L1. We now need to work out the “communication” between different cell types that is critical for preventing autoimmune diabetes.
“This finding increases our knowledge of how autoimmune forms of diabetes such as type 1 diabetes develop. It opens up a new potential target for treatments that could prevent diabetes in the future. Simultaneously, it gives new knowledge to the cancer immunotherapy field by uniquely providing the results of completely disabling PD-L1 in a person, something you could never manipulate in studies. Reducing PD-L1 is already effective for cancer treatment, and boosting it is now being investigated as a type 1 diabetes treatment — our findings will help accelerate the search for new and better drugs.”
Dr Lucy Chambers, Head of Research Communications at Diabetes UK, said: “Pioneering treatments that alter the behaviour of the immune system to hold off its attack on the pancreas are already advancing type 1 diabetes treatment in the USA, and are awaiting approval here in the UK.
“By zeroing in on the precise role of an important player in the type 1 diabetes immune attack, this exciting discovery could pave the way for treatments that are more effective, more targeted and more transformational for people with or at risk of type 1 diabetes.”
Helmsley Program Officer Ben Williams said: “New drugs often fail in development because scientific discoveries made in animal models don’t translate into humans. As such, drug developers strongly prefer to pursue new drugs where human genetic evidence supports the drug’s target. This study provides such compelling evidence that PD-L1 is a high-priority target to treat T1D, and should be pursued with the ambition of eventually reducing the burden of this difficult to manage disease.”
The paper is entitled ‘Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency’ and is published in the Journal of Experimental Medicine. The research was supported by the National Institute of Health and Care Research (NIHR) Exeter Biomedical Research Centre and The NIHR Exeter Clinical Research Facility.
New urine-based test detects high-grade prostate cancer, helping men avoid unnecessary biopsies

Researchers at the University of Michigan Rogel Cancer Center have developed a new urine-based test that addresses a major problem in prostate cancer: how to separate the slow-growing form of the disease unlikely to cause harm from more aggressive cancer that needs immediate treatment.
The test, called MyProstateScore2.0, or MPS2, looks at 18 different genes linked to high-grade prostate cancer. In multiple tests using urine and tissue samples from men with prostate cancer, it successfully identified cancers classified as Gleason 3+4=7 or Grade Group 2 (GG2), or higher. These cancers are more likely to grow and spread compared to Gleason 6 or Grade Group 1 prostate cancers, which are unlikely to spread or cause other impact. More than one-third of prostate cancer diagnoses are this low-grade form. Gleason and Grade Group are both used to classify how aggressive prostate cancer is.
Results are published in JAMA Oncology.
“Our standard test is lacking in terms of its ability to clearly pick out those who have significant cancer. Twenty years ago, we were looking for any kind of cancer. Now we realize that slow-growing cancer doesn’t need to be treated. All of a sudden, the game changed. We went from having to find any cancer to finding only significant cancer,” said co-senior study author John T. Wei, M.D., David A. Bloom Professor of Urology at Michigan Medicine.
Prostate-specific antigen, or PSA, remains the linchpin of prostate cancer detection. MPS2 improves upon a urine-based test developed by the same U-M team nearly a decade ago, following a landmark discovery of two genes that fuse to cause prostate cancer. The original MPS test, which is used today, looked at PSA, the gene fusion TMPRSS2::ERG, and another marker called PCA3.
“There was still an unmet need with the MyProstateScore test and other commercial tests currently available. They were detecting prostate cancer, but in general they were not doing as good a job in detecting high-grade or clinically significant prostate cancer. The impetus for this new test is to address this unmet need,” said co-senior author Arul M. Chinnaiyan, M.D., Ph.D., director of the Michigan Center for Translational Pathology. Chinnaiyan’s lab discovered the T2::ERG gene fusion and developed the initial MPS test.
To make MyProstateScore even stronger at identifying high-grade cancers, researchers used RNA sequencing of more than 58,000 genes and narrowed it to 54 candidates uniquely overexpressed specifically in higher-grade cancers. They tested the biomarkers against urine samples collected and stored at U-M through another major study, the National Cancer Institute’s Early Detection Research Network. This included about 700 patients from 2008-2020 who came for a prostate biopsy due to an elevated PSA level.
This first step narrowed the field to 18 markers that consistently correlated with higher grade disease. The test still includes the original MPS markers, plus 16 additional biomarkers to complement them.
From there, the team reached out to the larger Early Detection Research Network (EDRN), a consortium of more than 30 labs across the country that are similarly collecting samples. This ensured a diverse, national sampling. Knowing no specific details about the samples, the U-M team performed MPS2 testing on more than 800 urine samples and sent results back to collaborators at the NCI-EDRN. The NCI-EDRN team assessed MPS2 results against the patient records.
MPS2 was shown to be better at identifying GG2 or higher cancers. More importantly, it was nearly 100% correct at ruling out GG1 cancer.
“If you’re negative on this test, it’s almost certain that you don’t have aggressive prostate cancer,” said Chinnaiyan, S. P. Hicks Endowed Professor of Pathology and professor of urology at Michigan Medicine.
Moreover, MPS2 was more effective at helping patients avoid unnecessary biopsies. While 11% of unnecessary biopsies were avoided with PSA testing alone, MPS2 testing would avoid up to 41% of unnecessary biopsies.
“Four of 10 men who would have a negative biopsy will have a low risk MPS2 result and can confidently skip a biopsy. If a man has had a biopsy before, the test works even better,” Wei explained.
For example, a patient may get a prostate biopsy due to an elevated PSA, but no cancer is detected. The patient is followed over time and if his PSA inches up, he would typically need another biopsy.
“In those men who have had a biopsy before and are being considered for another biopsy, MPS2 will identify half of those whose repeat biopsy would be negative. Those are practical applications for patients out there. Nobody wants to say sign me up for another biopsy. We are always looking for alternatives and this is it,” Wei said.
MPS2 is currently available through LynxDx, which is University of Michigan spin-off company that has an exclusive license from the university to commercialize MPS2. Patients interested in learning more can call the Michigan Medicine Cancer AnswerLine at 800-865-1125.
The paper’s first authors are Jeffrey J. Tosoian, M.D., M.P.H., who is now at Vanderbilt University, and Yuping Zhang, Ph.D., and Lanbo Xiao, Ph.D., at U-M. Additional authors are Cassie Xie; Nathan L. Samora, M.D.; Yashar S. Niknafs, Ph.D.; Zoey Chopra; Javed Siddiqui; Heng Zheng, M.D.; Grace Herron; Neil Vaishampayan; Hunter S. Robinson, M.D.; Kumaran Arivoli; Bruce J. Trock, Ph.D.; Ashley E. Ross, M.D., Ph.D.; Todd M. Morgan, M.D.; Ganesh S. Palapattu, M.D.; Simpa S. Salami, M.D., M.P.H.; Lakshmi P. Kunju, M.D.; Scott A. Tomlins, M.D., Ph.D.; Lori J. Sokoll, Ph.D.; Daniel W. Chan, Ph.D.; Sudhir Srivastava, Ph.D.; Ziding Feng, Ph.D.; Martin G. Sanda, M.D.; Yingye Zheng, Ph.D.
Funding for this work is from the Michigan-Vanderbilt Early Detection Research Network Biomarker Characterization Center and Data Management and Coordinating Center, which are through the National Cancer Institute grants U2C CA271854 and U24 CA086368. Additional funding is from NCI grants P50 CA186786, R35 CA231996, U24 CA115102, U01 CA113913; Prostate Cancer Foundation; Howard Hughes Medical Institute; and the American Cancer Society.
Disclosures: Chinnaiyan serves on the advisory boards of Tempus, LynxDx, Ascentage Pharmaceuticals, Medsyn therapeutics, Esanik and RAAPTA therapeutics. Tomlins is an equity holder and chief medical officer of Strata Oncology. LynxDx has obtained an exclusive license from the University of Michigan to commercialize MPS2 and the TMPRSS2-ERG gene fusion. Tosoian and Chinnaiyan are equity holders and scientific advisers to LynxDx. Siddiqui, Zhang, Xiao and Niknafs have served as scientific advisers to LynxDx.
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Brian Cox Pulls Zero Punches When It Comes To Joaquin Phoenix’s ‘Appalling’ Napoleon Performance
Brian Cox’s assessment of Joaquin Phoenix’s performance in Napoleon was always Logan Roy-esque in its bluntness.
Earlier this week, the Succession star put in an appearance at HitFest where he was interviewed by BBC News anchor Clive Myrie.
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When the conversation turned to Ridley Scott’s recent Napoleon biopic – which divided opinion upon its release last year – the Emmy winner made his feelings clear.
“It’s terrible,” Brian said, as reported by the Evening Standard. “A truly terrible performance by Joaquin Phoenix. It really is appalling. I don’t know what he was thinking.
“I think it’s totally his fault and I don’t think Ridley Scott helps him. I would have played it a lot better than Joaquin Phoenix, I tell you that. You can say it’s good drama. No – it’s lies.”

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He added of Napoleon’s Oscar-winning star: “I think he’s well-named. Joaquin…wha-keen… wacky. It’s a sort of wacky performance.”
Brian was similarly critical of another historical drama, 1995’s Braveheart, branding it “a load of nonsense” and “a bollocks” (although he did praise Mel Gibson’s “wonderful” performance in the lead role).

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And as for Method acting, the controversial technique employed by his former co-star Jeremy Strong?
“Oh no that’s all bollocks. It’s a kind of nonsense,” he insisted. “We’re transmitters. That’s what we are as actors. We transmit energy.”
During a Town & Country magazine interview last year, Brian was similarly critical of Method acting, insisting his “fucking gifted” colleague should “celebrate [his] gift” and “go back to [his] trailer and have a hit of marijuana” rather than putting himself through so much in the name of acting.
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“It’s fucking annoying, don’t get me going on it…” he said of Jeremy’s technique.
‘Do You Think It’s Funny?’: Kay Burley Clashes With Grant Shapps Over Tory Sleaze

The Sky News presenter grilled the defence secretary after Mark Menzies became the latest Conservative MP to lose the party whip.
He is accused of using Tory campaign funds to pay off “bad people” he claimed had locked him in a flat, as well as for medical bills.
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Menzies, the MP for Flyde in Lancashire, denies the allegations but has agreed to “relinquish” the Tory whip while the party investigates the claims, which were first reported by The Times.
As Burley grilled Shapps on the claims, he said: “I thought I was coming on to talk about the situation in Iran and the Middle East.”
Burley replied: “We’ll come to that, Mr Shapps. In the next door constituency of Blackpool South, the whip was removed from Scott Benton over a lobbying scandal.
“Peter Bone, a former Conservative MP, [lost the whip] for sexual bullying, Neil Parish for viewing porn or was it tractors in the chamber of the House of Commons. Chris Pincher allegedly molesting men at the Carlton Club.
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“Eight independent MPs, former Tories. What is that saying about your party and the state of British politics this morning.”
Shapps said: “I understand what you’re driving at here. I thought I was coming on to talk about two wars in the world and you’re pressing me about some issues that I’m not particularly close to.”
As the defence secretary appeared to smirk, Burley asked him: “Do you think it’s funny, Mr Shapps?”
He replied: “I don’t think it’s funny, no one said it was funny, Kay.”
Burley said: “You seemed to be smirking about it. I’m asking you about the state of British politics this morning.”
The minister responded: “I’m not, you’re just pursuing a line of questioning about something which I didn’t come on to talk about because there two world wars, wars in the world, going on.”
Burley then interrupted him to point out: “They’re not world wars at the moment, Mr Shapps, and I’ll come onto those.
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“I want to ask you about your party’s previous Tory MPs. At least eight of them are now independent MPs and I’ve listed why they are not any longer representing their constituencies as members of the Conservative Party.
“I’m asking you what people in those constituencies should be thinking about the Conservative Party ahead of the next general election.”
A clearly-annoyed Shapps replied: “I think you’re trying to draw a thread between all of them. There are MPs from other parties who have experienced similar problems or misdemeanours and it’s right that there are processes in place, but I can’t really add much to this.”
Warwick Davis Pays Emotional Tribute Following The Death Of His Wife Samantha, Aged 53
Warwick Davis has announced the death of his wife of more than 30 years, Samantha, at the age of 53.
On Wednesday evening, the Star Wars performer shared a statement with BBC News confirming that Samantha, a fellow actor and the founder of the charity Little People UK, had died on 24 March.
Describing his wife as his “most trusted confidant and an ardent supporter of everything I did in my career”, Warwick said: “Her passing has left a huge hole in our lives as a family. I miss her hugs.”
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He continued: “She was a unique character, always seeing the sunny side of life she had a wicked sense of humour and always laughed at my bad jokes.”
“With her by my side, I was sure I could achieve anything, it was like having a super-power,” he added. “Without Sammy, there would have been no Tenable quiz show, no Willow series. No Idiot Abroad series three.”
Warwick and Samantha met in 1988 on the set of the film Willow, in which he played the titular sorcerer, and eventually married in 1991.
Their grown-up children, Harrison and Annabelle, told the BBC their mother’s “love and happiness carried us through our whole lives”.
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Dave J Hogan via Getty Images
Warwick and Samantha also had a son, Lloyd, who died just days after he was born, and another, George, who was stillborn.
As well as her charity work, Samantha appeared in the children’s TV show Through The Dragon’s Eye, and shared the screen with her husband in films like the comedy-horror Leprechaun 2 and the final film in the Harry Potter series.
She and her family also appeared in the ITV travel series Weekend Escapes With Warwick Davis in 2014.
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