Friday, January 23, 2026

 

ISSCR statement in response to new NIH policy on research using human fetal tissue 




International Society for Stem Cell Research




The abrupt ending of NIH support for fetal tissue research will undermine the development of new therapies for diseases that affect American families. Research with human fetal tissue (HFT) and HFT-derived cell lines has been integral to biomedical progress for nearly a century and has long been supported on a bipartisan basis under many U.S. administrations. This research has contributed to fundamental advances in understanding human development, infertility, infectious diseases, and chronic and neurodegenerative conditions. HFT-derived cell lines have played a critical role in the development of vaccines that have saved millions of lives worldwide.

This research is also governed by a well-established ethical and legal framework that includes rigorous scientific review, robust informed consent, and prohibition of profit from tissue donation. While continued investment in alternative research models is important and should be encouraged, HFT remains a necessary tool for addressing certain research questions that cannot yet be adequately answered by organoids, tissue chips, and other emerging technologies.

The announcement of this immediate change to NIH policy without prior engagement with the scientific community and without advance notice for ongoing, peer-reviewed projects is highly disruptive. Engagement with researchers in advance of policy changes helps ensure that NIH’s decisions are grounded in the latest scientific evidence and that the agency is fully informed about which lines of research may be constrained or lost due to its changes in oversight. Immediate withdrawal of research support risks the loss of life-saving biomedical research and undermines responsible stewardship of public resources.

We urge reconsideration of this policy and call for NIH to engage constructively with the scientific community to support biomedical research that advances discovery and improves human health.

About ISSCR
Across more than 80 countries, the International Society for Stem Cell Research (@ISSCR) is the preeminent global, cross-disciplinary, science-based organization dedicated to advancing stem cell research and its translation to medicine.

 

Biologists and engineers follow goopy clues to plant-wilting bacteria




University of California - Davis
Biologists and Engineers Follow Goopy Clues to Plant-Wilting Bacteria 

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Ralstonia bacteria cause rapid wilting and death in plants. The bacteria also make an unusually fluid "goopy" secretion. A collaboration between UC Davis plant scientists and engineers shows that this goop is a viscoelastic fluid and that its properties help the bacteria spread rapidly in a host plant. 

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Credit: Jael Mackendorf, UC Davis




Slippery, drippy goop makes Ralstonia bacteria devastating killers of plants, causing rapid wilting in tomato, potato and a wide range of other crops, according to new research. The work, published Jan. 22 in Proceedings of the National Academy of Sciences, comes from an unusual collaboration between plant pathologists and engineers at the University of California, Davis. 

Ralstonia solanacearum can lurk in damp soils for years before infecting a plant, spreading rapidly through the water-carrying vessels (xylem). Infected plants wilt and die within days. 

“My analogy is that they cause a heart attack for plants, because they clog up the vessels and cause plants to wilt and die,” said Tiffany Lowe-Power, associate professor of plant pathology in the UC Davis College of Agricultural and Environmental Sciences. 

Like many bacteria, Ralstonia colonies can secrete a film or coat around themselves. Typically, these films help trap or conserve moisture. In the case of Ralstonia, this secreted film is unusually sloppy and can make them quite difficult to work with, Lowe-Power said. 

“Ralstonia are charismatically disgusting, there's this like, real grossness to them,” she said.

Ralstonia’s secreted film is made up of a long, sugar-like molecule called exo polysaccharide 1 (EPS-1). It has been known that EPS-1 is somehow tied to Ralstonia’s ability to kill plants. But how? 

“With the ways that microbiologists and geneticists go about answering questions, we are able to get somewhat close, but not really to the mechanism,” Lowe-Power said. “We need a physicist.” 

Hari Manikantan, associate professor in the UC Davis Department of Chemical Engineering, studies the mechanics and dynamics of complex multiphase fluids. 

“I love goop of all forms -- saliva, foams, lung surfactants, tears,” Manikantan said. 

Goopy fluids are both viscous and elastic in different degrees. Elasticity measures whether a material can snap back after being stretched. Viscosity measures how easily it flows. 

Silly putty, for example, is elastic over a short time scale. 

“You bounce it, it’s a perfectly solid object. If you keep it on a table, it slowly flows out over minutes to hours,” Manikantan said. “The question is what's the relevant time scale.”

A mutual love of goop

Manikantan and Lowe-Power discovered their mutual love of goop when they met during a new faculty training before the pandemic. Using equipment in Manikantan’s laboratory, they were able to make highly precise measurements of the viscoelastic properties of secretions collected from Ralstonia colonies by Matthew Cope-Arguello, a graduate student in Lowe-Power’s lab. 

They discovered that the goop from pathogenic Ralstonia flows easily under the kind of shear forces that would be found in the xylem vessels of plants. This allows the bacteria to spread rapidly throughout an infected plant. 

How common is this trait? Cope-Arguello developed a simple test. If you grow bacteria making a biofilm on a plate and hold the plate at an angle, does it drip? They looked at other Ralstonia strains, including those that don’t make EPS-1, and also asked colleagues around the country to test other bacteria that are evolutionary cousins of the Ralstonia wilt pathogens. 

“We were really able to show, both from the data that our collaborators collected as well as data that we mined through publicly available genomes, that this polysaccharide is unique to the plant pathogens,” Cope-Arguello said. 

For biologists, the research shows why EPS-1 makes these bacteria especially pathogenic. For engineers and soft matter physicists, it provides an experimental system to study. 

“Now we have this actual relevant change that's guided by genetics that my community can begin to mathematically model. So I'm very excited about how this feeds back into that soft matter physics world,” Manikantan said. 

Additional coauthors are: Jiayu Li, Nathali Aoun, Tabitha Cowell and Samantha Wong at UC Davis; Zachary Konkel and Jonathan Jacobs, The Ohio State University; Nicholas Wagner and Tuan Tran, University of South Alabama; A. Lin Han Chan and Kristen DeAngelis, University of Massachusetts, Amherst; Lan Thanh Chu and Loan Bui, University of Dayton, Ohio; Mariama Carter and Caitlyn Allen, University of Wisconsin-Madison; Lindsay Caverly, University of Michigan Medical School; Matthew Wargo, University of Vermont. 

The work was supported in part by grants from the Academic Senate at UC Davis, the U.S. Department of Agriculture and the National Science Foundation. 

 

Jumping giants: Fossils show giant prehistoric kangaroos could still hop




University of Bristol
Jumping giants: Fossils show giant prehistoric kangaroos could still hop 

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Reconstruction of Sthenurine Hopping.

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Credit: Megan Jones




Scientists studying the fossil remains of giant prehistoric kangaroos have found that even animals weighing more than 200kg may not have been too big to bounce, overturning long-held assumptions about the limits of hopping.

Today, the red kangaroo is the largest living hopping animal and weighs around 90kg. But during the Ice Age, some kangaroos grew more than twice the size of that - some reaching up to 250kg.

For years, researchers believed these giants must have abandoned hopping, as earlier studies suggested that hopping would become mechanically impossible above about 150kg. Those conclusions were largely based on simply scaling up modern kangaroos, which scientists from the University of Manchester, in collaboration with the University of Bristol and the University of Melbourne suspected might be misleading.

Now, by combining measurements from living kangaroos with direct evidence from fossil bones, the new study, published today in the Nature journal Scientific Reports finds that giant kangaroos may have been capable of hopping.

Lead researcher Megan Jones, Postgraduate Researcher at the University of Manchester, said: “Previous estimates were based on simply scaling up modern kangaroos, which may mean we miss crucial anatomical differences. Our findings show that these animals weren’t just larger versions of today’s kangaroos, they were built differently, in ways that helped them manage their enormous size.”

The team examined two potential limiting factors for hopping - the strength of the foot bones and the ability of the ankle to anchor the powerful tendons that drive a hop.

Their analysis show that the giant kangaroos had shorter, thicker foot bones capable of withstanding landing forces and their heel bones were broad enough to support much thicker ankle tendons than those of modern kangaroos.

However, these giants probably did not bounce across the landscape like today’s red kangaroos.

“Thicker tendons are safer, but they store less elastic energy,” explained Dr Katrina Jones, Royal Society Research Fellow at the University of Bristol.

 “This likely made giant kangaroos slower and less efficient hoppers, better suited to short bursts of movement rather than long-distance travel. But hopping does not have to be extremely energy efficient to be useful, these animals probably used their hopping ability to cross rough ground quickly or to escape danger.”

The fossil analysis also revealed a range of locomotion strategies among the extinct species. Some giant kangaroos may have mixed hopping with other forms of movement, including walking upright on two legs, or moving on all fours, suggesting that hopping was just one part of a broader “movement repertoire”.

But the diversity of prehistoric Australia extends beyond just movement.

Dr Robert Nudds, Senior Lecturer in Evolution, Infection and Genomics at the University of Manchester, said: “Our findings contribute to the notion that kangaroos had a broader ecological diversity in prehistoric Australia than we find today, with some large species grazers like modern kangaroos while others were browsers – an ecological niche not seen in today’s large kangaroos.” 

The findings provide the most comprehensive assessment to date of the mechanical feasibility of hopping in giant extinct kangaroos.

Sthenurine skeleton in the South Australian Museum.

Credit

Megan Jones


Heel bone of the largest giant kangaroo species, Procoptodon goliah.

Credit

Photos are by Megan Jones and the specimen is from UCMP, Berkeley (please credit both Megan and UCMP)

 

PBM profits obscured by mergers and accounting practices, USC Schaeffer white paper shows



Requiring more financial transparency from PBMs would help policymakers understand how money flows through the large healthcare companies that now own them



University of Southern California




Pharmacy benefit managers (PBMs) under the microscope for their role in high drug prices have often cited their reportedly slim profit margins as evidence that they do not drive up costs. The three leading PBMs, which control about 80% of the prescription drug market, have historically reported profit margins of 4% to 7%, among the lowest in the healthcare industry.

A new white paper from the USC Schaeffer Center for Health Policy & Economics demonstrates that these slim margins are dramatically influenced by the accounting practices PBMs elect to employ. The paper also shows how efforts to assess PBM profits have become more challenging after these companies merged with healthcare conglomerates that own other players in the pharmaceutical supply chain.

States in recent years have advanced or considered numerous measures seeking to increase PBM transparency, and Congress is currently pursuing legislation to reform PBM practices. The Federal Trade Commission, meanwhile, continues to scrutinize PBMs after accusing leading firms of inflating drug costs through strategies like rebates, markups and preferential treatment of affiliated pharmacies.

“Accounting practices make it difficult to judge the health and efficiency of the PBM market, particularly as dominant firms have become part of larger, more complex companies,” said lead author Karen Mulligan, a research scientist at the Schaeffer Center. “Greater financial disclosure requirements for PBMs are needed to develop a better picture of how PBMs make money and the extent to which these practices may raise costs for consumers.”

How accounting choices drive margins

PBMs sit at the center of the pharmaceutical supply chain, acting as intermediaries that pay pharmacies and negotiate rebates with drug manufacturers on behalf of insurers. PBMs retain transaction fees and a portion of manufacturer rebates while passing along payments between manufacturers, insurers and pharmacies.

Historically, PBMs have included these “pass-through payments” in financial reporting. This may also include the share of rebates sent directly to the insurer. While allowed under professional accounting guidelines, this practice may add hundreds of billions of dollars to PBMs’ reported revenue or expenses without affecting their actual earnings. This obscures key determinants of PBMs’ profitability, including the role of rebates, fees and other payments.

Using a simplified example with typical transaction fees and rebates, the white paper illustrates how accounting choices can produce vastly different profit margins for a hypothetical drug listed at $360. If pass-through payments were reported as revenues or expenses, the PBM’s margin would be 10% – or slightly higher at 13% if manufacturer rebates passed to the insurer were not reported. However, the margin jumps to 87% if pass-through payments were not reported at all. (See Figure 5 in the white paper.)

Vertical integration in the healthcare industry has further blurred PBMs’ financial picture. In the past decade, the three dominant PBMs have become part of diverse healthcare corporations that also own insurers, specialty pharmacies and group purchasing organizations (GOPs) that negotiate discounts.

Under this structure, payments between the PBM, insurer and the specialty pharmacy become internal transfers invisible to the public. Using the same hypothetical $360 drug as the previous example, the white paper shows how the publicly reported profit margin can be half of what’s recorded internally, as dollars are shifted to other units within the PBM’s parent company. (See Figure 6.)

Transparency reforms should illuminate revenue streams

The researchers suggest that policymakers consider requiring PBMs to exclude pass-through payments from financial reporting, as regulators have done for intermediaries in other industries.

Policymakers should also consider reforming financial reporting requirements so that healthcare conglomerates provide separate reporting for each distinct business unit, rather than allowing PBM operations to be combined with other units like specialty pharmacy. Further, requiring disclosure of internal transfers and pass-through payments in these companies would provide clarity about what’s driving profits.

“True transparency requires greater visibility into profit flows hidden inside increasingly complex corporate structures,” said co-author Darius Lakdawalla, chief scientific officer at the Schaeffer Center and the Quintiles Chair of Pharmaceutical Development and Regulatory Innovation at the USC Mann School. “Building a more efficient and sustainable pharmaceutical supply chain starts with a better understanding of where dollars are flowing.”

Missing Medicare data alters hospital penalties, study finds



Hospitals in areas with high Medicare Advantage enrollment face inflated financial penalties for readmissions, because government uses only traditional Medicare data



Michigan Medicine - University of Michigan




For more than a decade, hospitals have worked to help older adults avoid repeated inpatient stays, incentivized by a federal program that cuts Medicare reimbursements if hospitals have higher-than-expected rates of readmissions for people with certain conditions.

The Hospital Readmissions Reduction Program has helped spur innovation, including initiatives to better prepare patients and their families to manage care after hospitalization, and to support them virtually at home.

But a new University of Michigan study finds that these financial penalties have hit some hospitals harder than they should, even if those hospitals have done a reasonable job at keeping people with heart failure, pneumonia and other serious conditions from ending up back in a hospital within a month of leaving one.

Such hospitals have been paying inflated readmission penalties for a seemingly unrelated reason: They happen to serve higher percentages of older adults who have chosen to enroll in Medicare Advantage plans run by private insurance companies.

So what’s the connection?

Currently, the federal government only grades hospitals on their readmission performance for older adults with traditional Medicare, which is run by the federal government. Data from Medicare Advantage are not currently included in the calculations that determine these penalties.

This is a problem, because Medicare Advantage enrollees tend to be healthier than traditional Medicare beneficiaries. But the readmission penalty program’s risk-adjustment is unable to capture these differences.

So, the researchers find, hospital performance looks worse for hospitals treating fewer traditional Medicare beneficiaries and more Medicare Advantage enrollees, even if those hospitals take the same actions to prevent readmissions as other hospitals.

The study, published in JAMA Network Open, suggests that not incorporating Medicare Advantage data results in an unwarranted redistribution of nearly $300 million a year in readmission penalties across hospitals nationwide. That’s more than half the total amount of readmissions penalties incurred each year across all hospitals.

Penalties are publicly reported every year and covered by the news media.

The Centers for Medicare and Medicaid Services has issued a rule to begin using Medicare Advantage data in the program. But even when it takes effect later this year, it will not affect hospital penalties for several years.

An unintended consequence with major consequences

The analysis shows an unintended consequence of the intersection between two major health policies of the last 15 years: the rapid rise in Medicare plan enrollment, and the HRRP, says senior author Geoffrey Hoffman, Ph.D., a professor at the U-M School of Nursing and member of the U-M Institute for Healthcare Policy and Innovation.

“Medicare Advantage has experienced extraordinary growth in the past decade, yet policymakers haven’t caught up with implications of this growth for Medicare payment policy that is based purely on traditional Medicare enrollment,” says Hoffman. “The omission of Medicare Advantage data highlights the continuing issue of inadequate measurement of patient risk in the Hospital Readmission Reduction Program, with important implications for the penalties that hospitals face.”

When the HRRP started calculating readmission rates in 2012, only 29% of older adults and people with disabilities chose Medicare Advantage plans.

Today, it’s 54%. But the distribution is not even across the country.

Hoffman and lead author Zoey Chopra, M.A., mapped that distribution and divided more than 3,200 hospitals into five groups based on the MA enrollment levels in 1,486 counties.

Chopra is working toward both a medical degree in the U-M Medical School and a Ph.D. in economics in the U-M College of Literature, Science and the Arts. He is a Medical Scientist Training Program fellow at the Medical School.

Differences in hospitals and populations

The hospitals in the areas with the highest Medicare Advantage enrollment were much more likely to be larger, nonprofit, teaching-oriented and in urban areas than hospitals in the areas with the lowest levels of Medicare Advantage enrollment.

Even when the researchers took into account an aspect of the readmission penalty program that only judges hospitals against groups of their peer hospitals, they still found that the Medicare Advantage enrollment rate mattered.

Past studies have shown that older adults who choose Medicare Advantage plans tend to be in the younger age range of eligibility, and to have fewer serious health conditions.

Hoffman has studied patterns of migration back to traditional Medicare by adults who had previously chosen Medicare Advantage plans, and factors that cause older adults to leave a Medicare Advantage plan for another Medicare Advantage plan or traditional Medicare.

Even though the readmission penalty program adjusts penalties based on the health risks of hospitals’ patients with the conditions that are included in the program, the lack of Medicare Advantage data could be a source of bias, he said.

Areas with more Medicare Advantage enrollees may end up with higher-risk traditional Medicare beneficiaries, because healthier enrollees migrate to Medicare Advantage. But those risk differences can’t be captured in the data models used by CMS. Therefore, by basing the program’s penalties only on traditional Medicare enrollees, hospitals with more Medicare Advantage patients are at greater, unwarranted risk of readmission penalties.

“Our study observes an inadvertent consequence of restricting the readmissions program to traditional Medicare participants,” said Chopra. “At the time of the HRRP’s rollout, this made sense, given lower enrollment and concerns about accuracy of the Medicare Advantage data. However, including Medicare Advantage data now appears imperative to avoid unnecessary penalties for hospitals treating relatively more private pay patients.”

Potential solutions

The new policy taking effect later this year rule will add Medicare Advantage data to HRRP calculations of readmissions, but Hoffman and Chopra have concerns about the completeness of what may be available. Risk-coding and policy differences across Medicare Advantage and traditional Medicare could also complicate comparisons of hospital performance.

It will also base penalties on the last two years’ worth of readmission data, instead of three. While the inclusion of Medicare Advantage data nearly doubles the amount of data used for comparisons, given concerns about data completeness and accuracy, this change may nonetheless make it harder statistically to see how hospitals have really done on keeping readmissions as low as possible, Hoffman said.

In addition to the rule, they suggest, CMS could consider factoring the percentage of Medicare Advantage enrollees in a hospital’s area or patient base into the calculations for its readmission rate and potential penalty.

The study was funded by the National Institute on Aging of the National Institutes of Health (RO1AG074944, T32AG000221). Chopra’s funding is through the Population Studies Center at the U-M Institute for Social Research. Andrew Ryan, Ph.D., of Brown University is a co-author of the study.

Hospital Readmission Reduction Program Penalties for Hospitals with High Medicare Advantage Penetration, JAMA Network Open, DOI:10.1001/jamanetworkopen.2025.54972