Tuesday, May 12, 2026

 

CDI convenes leaders in translational immunology



From T Cell exhaustion to vaccine interception, the Applied Immunological Research Symposium (AIRS) unites renowned scientists in advancing cancer immunotherapy.




Hackensack Meridian Health

CDI AIRS Symposium 2026 

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The speakers at the third annual Applied Immunological Research Symposium (AIRS) at the Hackensack Meridian CDI.

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Credit: Hackensack Meridian Health






NUTLEY, N.J. – The Hackensack Meridian Center for Discovery and Innovation (CDI) leveraged its continued platform as a nexus for research by hosting its third annual Applied Immunological Research Symposium (AIRS).

The symposium was held at the CDI’s state-of-the-art facility in a bid to bridge the gap between advanced immunological research and its practical application for patient care. The vehicle for this central message was the Center’s focus on innovation and translational science in cellular immunotherapy 

The event brought together a world-class assembly of scientists to share groundbreaking findings aimed at accelerating the next generation of cancer immunotherapies.

According to David Perlin, Ph.D., chief scientific officer and executive vice president of the CDI, “this symposium is a direct reflection of our mission to create a dynamic, collaborative environment translating promising research into clinical practice.”

Flipping the Switch

Keynote speaker and world-renowned immunologist Rafi Ahmed, Ph.D., of Emory University, provided the event’s centerpiece with his keynote address, "What is T Cell Exhaustion?"

In a two-part presentation, Dr. Ahmed first explained the science of T cell exhaustion, where immune cells are "switched off" by inhibitory receptor PD-1—an immune checkpoint protein found on T Cells that acts as that “switch” to turn off immune responses—during chronic disease. 

He then connected this science to patient care, presenting clinical data in oncology patients with the Human Papillomavirus (HPV-positive). His data showed how blocking this PD-1 switch reawakens a core population of "stem-like" T cells, unleashing them to fight disease as the body shifts its natural reaction to an acute infection becoming chronic. 

“Big decisions have to be made early,” marveled Dr. Ahmed during his presentation. He’d continue that our immune systems are “always prepared for chronic, but adjust to acute, infection.”

After an amusing anecdote about collaborating with CDI scientist and colleague Hai-Hui “Howard” Xue, M.D., Ph.D., who provided his own animal models to help with the research process after a quick airport phone call, Dr. Ahmed concluded that these studies have further treatment implications in cancer treatment, a myriad of chronic infections, and various autoimmune diseases.

“Dr. Ahmed’s work has fundamentally reshaped our ability to treat diseases that were once considered intractable,” said Binfeng Lu, Ph.D., director of the CDI’s Institute for Immunologic Intervention (3i) and one of the symposium organizers. “His pioneering work on T cell exhaustion established a foundational conceptual framework for modern immunology and oncoimmunology, and is already saving lives by guiding the development of transformative therapies.”

The Common Threads: Weaving the Science Together

Dr. Ahmed’s address set the stage for a day of robust scientific exchange, featuring presentations from leaders at top research institutions nationwide. 

Key studies and their talking points included:

  • Yi Zhang, M.D., Ph.D., Center for Discovery and Innovation: Dr. Zhang—also one of the symposium organizers—presented novel strategies for the epigenetic reprogramming of T cells. He highlighted the importance of the EZH2 gene in CAR T cell therapy and in tumor control. His work offers a pathway to enhance cancer immunotherapy while simultaneously preventing graft-versus-host disease (GvHD) in transplant patients.

  • Dean Lee, M.D., Ph.D., Nationwide Children's Hospital: Dr. Lee discussed the creation of a universal-donor manufacturing platform for NK and CAR-NK products, especially in pediatric cancers such as leukemia, where treatments such as bone marrow transplant is essential. This breakthrough is a crucial step toward making advanced, off-the-shelf cell therapies more accessible and affordable in multi-site clinical trials.

  • Geoffrey R. Hill, M.D., Fred Hutchinson Cancer Center: Dr. Hill explored complex regulatory networks that govern patient responses to cancer immunotherapy, specializing in the EOMES gene (short for eomesodermin) in commanding T Cell and NK cell cancer response against acute graft-vs.-host disease. While imploring the need for more human studies, he provided key insights into overcoming therapeutic resistance, improving patient outcomes.

  • Olivera J. Finn, Ph.D., University of Pittsburgh School of Medicine: Dr. Finn outlined her pioneering research in developing vaccines for human cancer interception, a triumph in the face of discouraging results over decades of vaccine studies for cancer-therapeutic use. Her work—in itself, an inspiring message of perseverance in the field—presented a shift from treatment to proactive prevention in the fight against cancer.

  • Ming Li, Ph.D., Memorial Sloan Kettering Cancer Center: Dr. Li detailed the fundamental immunological mechanisms of cancer defense. His laboratory’s findings are uncovering new molecular targets to bolster the body’s natural ability to fight tumors. His presentation ended with the suggestion that we “go beyond checkpoint inhibitors” to continue meeting unmet needs in immunotherapy.

The event concluded with one cohesive message: 

The future of cancer treatment lies in collaborative, translational research across public and private sectors.

“We’re passionate about providing a forum for the brightest minds in immunology,” said Dr. Perlin, also a professor of Medical Sciences at the Hackensack Meridian School of Medicine. “By convening such a powerful collection of scientific leaders, the CDI affirms its central role in the global effort to bridge the academic and clinical gap in fighting the world’s most challenging diseases.”

 

The birds and the babies: Humans and zebra finches have a similar technique for learning to speak #ASA190



Humans and zebra finches both rely on caregiver reinforcement to learn complex vocalizations




Acoustical Society of America

Researchers can use zebra finches as a model for infant language development 

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Since zebra finches are similar to humans in how they learn to communicate, researchers can use them as a model for infant language development.

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Credit: Michael H. Goldstein





PHILADELPHIA, May 11, 2026 — We are all born completely helpless, with little of the knowledge and skills we will need to survive as adults. Even our ability to communicate is almost entirely learned from our parents or caregivers.

Some animals are the same. Zebra finches, in particular, are so similar to humans in how they learn to communicate that researchers often study them to better understand how we develop language.

To help answer these questions, Steven Elmlinger, from Princeton University, will present his research on early vocalizations in both human infants and zebra finches Monday, May 11, at 1 p.m. ET as part of the 190th Meeting of the Acoustical Society of America, running May 11-15.

Elmlinger studies vocal learning, piecing together how individuals develop and change their vocalizations to interact with others. He conducted three studies, two with human infants and one with finches, to understand how immature babbling transitions into adultlike speech.

In the first experiment, he observed infants interacting with their caregivers, noting that adults respond more to sequential vocalizations comprising multiple syllables than single syllable vocalizations. In the second study, he observed 30 infants across a period of several months to determine the role that these caregivers play in helping infants learn sequential vocalizations.

“We might assume that early learning of vocal sequences is primarily driven by motor practice,” said Elmlinger. “Prior research suggests social feedback guides infants’ vocal advances at the level of individual syllables. Here we wanted to know if social feedback also influences infants’ vocal sequence development.”

In this study, he and his colleagues found that caregiver responses to sequential vocalizations significantly increased the rate at which infants learned to produce those sequences. By encouraging complex vocalizations, caregivers could help their children learn faster.

In the third study, Elmlinger repeated this experiment with zebra finches, with the same finding. Like humans, zebra finches use social feedback to teach their young.

“Taken together, our results suggest that not only do both humans and zebra finches use social feedback to guide advances in the acoustics of their vocal repertoire, but their social environment also guides low-level temporal foundations of their vocal communication,” said Elmlinger.

When it comes to language learning, humans are not as unique as we once thought. At least one other species learns to vocalize in the same way we do, and there may be others awaiting discovery.

“I would love to collaborate with new-world monkey, cetacean, and bat scientists,” said Elmlinger. “There are good hints that at least some of these animals should show socially guided vocal learning as well — perhaps it is not rare, just understudied.”

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Main Meeting Website: https://acousticalsociety.org/philadelphia/

Technical Program: https://eppro01.ativ.me/web/planner.php?id=ASASPRING2026

ASA PRESS ROOM

In the coming weeks, ASA’s Press Room will be updated with newsworthy stories and the press conference schedule at https://acoustics.org/asa-press-room/.

LAY LANGUAGE PAPERS

ASA will also share dozens of lay language papers about topics covered at the conference. Lay language papers are summaries (300-500 words) of presentations written by scientists for a general audience. They will be accompanied by photos, audio, and video. Learn more at https://acoustics.org/lay-language-papers/.

PRESS REGISTRATION

ASA will grant free registration to the in-person conference at the Philadelphia Marriott Downtown for credentialed and professional freelance journalists. If you are a reporter and would like to attend the meeting and/or press conferences, contact AIP Media Services at media@aip.org. For urgent requests, AIP staff can also help with setting up interviews and obtaining images, sound clips, or background information.

ABOUT THE ACOUSTICAL SOCIETY OF AMERICA

The Acoustical Society of America is the premier international scientific society in acoustics devoted to the science and technology of sound. Its 7,000 members worldwide represent a broad spectrum of the study of acoustics. ASA publications include The Journal of the Acoustical Society of America (the world’s leading journal on acoustics), JASA Express Letters, Proceedings of Meetings on Acoustics, Acoustics Today magazine, books, and standards on acoustics. The society also holds two major scientific meetings each year. See https://acousticalsociety.org/.

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Oxytocin linked to group competition




University of Zurich
Oxytocin Linked to Group Competition 

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Oxytocin also plays a significant role in team competitions. Oxytocin levels rose most sharply following matches against well-known rivals.

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Credit: University of Zurich






Oxytocin – often referred to as the “love hormone” – also plays a role in competitions between groups, a new study led by Charlotte Debras and Adrian Jaeggi from UZH’s Institute of Evolutionary Medicine shows. “Previous work showed that receiving oxytocin via a nasal spray can make people more ‘groupish’,” says Debras, who conducted the study as part of her doctoral research. “But it wasn’t known whether OT naturally increased during group competition.”

Oxytocin levels linked to social context

To systematically study competition, the researchers organized football tournaments together with the Indigenous Tsimane’ people in the Bolivian Amazon. “The Tsimane’ lifestyle has an effect on their hormone levels,” says Jaeggi, who has been conducting research on site since 2011. For example, levels of reproductive hormones like testosterone or progesterone are lower when calories are harder to come by. Meanwhile, the kinds of social factors linked to OT are likely especially important in these highly interdependent societies. To test their hypothesis, the researchers measured oxytocin levels in the urine of football players before and after the matches.

Oxytocin levels increased most strongly after matches against familiar rivals but less so among teams from different communities. When Tsimane’ played against non-Tsimane’ people, however, the increase was again higher. “This suggests that oxytocin is sensitive to the salience of the opposition – showing heightened reactivity both toward familiar competitors and toward a clearly defined out-group,” says Jaeggi.

Higher oxytocin levels in men

One particularly striking finding of the study was that women’s OT levels did not differ before or after games, unlike men’s. Debras mentions several possible explanations for this. “Firstly, women start from higher baseline levels, as many of them were breastfeeding, which could make it harder to detect a change.” It is also possible that football may not hold the same significance for women, as they play less often than men. Another explanation is provided by the “male warrior hypothesis,” which proposes that men have evolved to be generally more invested in group competition. “The most important forms of rivalry for Tsimane’ women may involve relational dynamics, such as managing reputations or jostling for social support, rather than physical competition,” says Debras.

Relevant for cooperation and group boundaries

The study does not make it possible to determine whether the increase in OT primarily promotes cohesion within the team or competition with the opposing group. In team sports, both aspects are closely intertwined. “Cooperation can be a successful way to compete in the game of life, and OT seems to be a key ingredient for this,” says Jaeggi. “OT has been linked to group conflict in many different species, from fish to chimpanzees. Our findings suggest that similar mechanisms are at play in humans.” 

Literature
Charlotte C. Debras et al. Us against Them: Oxytocin Response to Competition in a Small-Scale Human Society. Proceedings of the Royal Society B. 6 May, 2026. DOI: https://doi.org/10.17605/OSF.IO/UK8PA

Contact 

Prof. Adrian V. Jaeggi
Institute of Evolutionary Medicine
University of Zurich
Tel. +41 44 635 05 40
E-mail: adrian.jaeggi@iem.uzh.ch

 

Probing links between decision-making and mental resilience


Some people display differences in brain responses to rewards and costs from choices they make that are associated with higher psychological resilience.



Society for Neuroscience






Whether people are mulling over the pros and cons of a purchase or assessing their interactions with new people, they may show a bias in placing more value on perceived positive or negative information. In a new JNeurosci paper, Ulrike Basten and colleagues, from RPTU University Kaiserslautern-Landau and the University of Amsterdam, explored whether individual differences in processing benefits and costs are linked to psychological resilience. 

The researchers presented 82 participants with images of different colored shapes. Colors and shapes were associated with gains or losses that culminated in real earned money or costs at the end of the experiment. Given the same presentation of different colored shapes, some participants generally put less value on minor losses, which led them to accept more of the offers. Emphasizing this point further, says Basten, “These individuals don’t put more value on rewards, they put less value on negative consequences and have a higher tendency to accept offers with mixed consequences. How they process negative information is different.” Why might this be the case? The researchers found that participants who put less value on minor losses had stronger increases in prefrontal brain activity to the losses and more reduced activity when they received gains. These brain response differences mediated the link between the acceptance bias in decision-making and higher self-reported psychological resilience. 

According to the researchers, their work suggests that stronger prefrontal brain responses to negative information may enable people to control their thoughts and feelings about losses. This control may be what makes these people more psychologically resilient. Says Basten, “We can’t claim causality from our findings, so one next step could be to manipulate the bias by rewarding certain answers—essentially training people to show more positive bias in decision-making—and see if that leads to better resilience.” 

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Please contact media@sfn.org for full-text PDF. 

About JNeurosci 

JNeurosci was launched in 1981 as a means to communicate the findings of the highest quality neuroscience research to the growing field. Today, the journal remains committed to publishing cutting-edge neuroscience that will have an immediate and lasting scientific impact, while responding to authors' changing publishing needs, representing breadth of the field and diversity in authorship. 

About The Society for Neuroscience 

The Society for Neuroscience is the world's largest organization of scientists and physicians devoted to understanding the brain and nervous system. The nonprofit organization, founded in 1969, now has nearly 35,000 members in more than 95 countries. 

 

Can new research findings help overcome challenges to malaria treatment?




Wiley






Research published in The FEBS Journal may help overcome challenges to the treatment of malaria—a tropical disease caused by infection of red blood cells with Plasmodium parasites, which are transmitted through infected mosquito bites. The research is based on a strategy that targets an enzyme specific to the parasite, Falcipain-2 (FP2), which is essential for parasite survival and growth within the host.

FP2 allows the parasite to digest human hemoglobin so that it can replicate inside red blood cells, which leads to severe malaria symptoms, including red blood cell destruction. Although FP2 is parasite-specific, it is highly similar to a class of human enzymes called cathepsins. This study therefore sought to determine the detailed structural and functional characterizations of FP2 so that it could be targeting without harming cathepsins.

Previously, the researchers identified that polyethylene glycol (PEG) can form stable interactions with FP2. In this latest study, they focused on how different PEG molecules bind to FP2 and its target, hemoglobin. Their computational analyses identified a binding region, or pocket, of a particular PEG called PEG400 with FP2. This pocket exhibits minimal conservation in human cathepsins. PEG400 was capable of binding FP2 and affecting its digestion of hemoglobin.

“The findings pave the way for designing and incorporating new small molecule inhibitors of FP2 activity, suggesting opportunities for selective antimalarial therapies with a cumulative benefit of reducing off-target specificity,” said corresponding author Sampa Biswas, PhD, who conducted this work while at the Saha Institute of Nuclear Physics, in India, and is currently at InBOL (Indian Barcode of Life) Health Care.

URL upon publication: https://onlinelibrary.wiley.com/doi/10.1111/febs.70546

 

Additional Information
NOTE:
 The information contained in this release is protected by copyright. Please include journal attribution in all coverage. For more information or to obtain a PDF of any study, please contact: Sara Henning-Stout, newsroom@wiley.com.

About the Journal
The FEBS Journal is a multidisciplinary, non-profit society journal that publishes full-length high-quality papers and expert reviews relevant to the molecular, cellular and biochemical life sciences. The journal is free to publish in, while offering open-access options.

About Wiley      
Wiley is a global leader in authoritative content and research intelligence for the advancement of scientific discovery, innovation, and learning. With more than 200 years at the center of the scholarly ecosystem, Wiley combines trusted publishing heritage with AI-powered platforms to transform how knowledge is discovered, accessed, and applied. From individual researchers and students to Fortune 500 R&D teams, Wiley enables the transformation of scientific breakthroughs into real-world impact. From knowledge to impact—Wiley is redefining what's possible in science and learning. Visit us at Wiley.com and Investors.Wiley.com. Follow us on FacebookXLinkedIn and Instagram.

 

BRIGHT and LanzaTech launch new partnership to accelerate carbon to value biotechnology in Europe



A multi-year collaboration will establish a next-generation C1 biofoundry at DTU to convert industrial carbon emissions into fuels, chemicals, and materials



Technical University of Denmark

Biofoundry inside 

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Biofoundry inside. Photo: BRIGHT.

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Credit: BRIGHT





SKOKIE, IL., May 5, 2026 - BRIGHT, the Novo Nordisk Foundation Biotechnology Research Institute for the Green Transition at the Technical University of Denmark (DTU), and LanzaTech Global, Inc. (NASDAQ: LNZA) (“LanzaTech”), a global leader in gas fermentation, have entered a multi‑year agreement to accelerate development of technologies that convert carbon emissions into valuable products.

The partnership runs until April 2028 and includes the design and installation of a next‑generation C1 biofoundry at DTU. This allows LanzaTech to extend its world-class synthetic biology expertise, leveraging BRIGHT’s infrastructure, talent, and regional reach. At the same time, DTU will gain the tools and expertise needed to establish Denmark and Europe as an important player in the emerging field of carbon‑to‑value biotechnology, accelerating innovation in the field of circular and competitive bioeconomy.

“DTU has a history of driving innovation from the lab to commercial deployment. Our new partnership with LanzaTech emphasizes our commitment to accelerate bio-solutions innovation for the benefit of Denmark, Europe and beyond,” says DTU provost, Christine Nellemann.

 

From carbon emissions to sustainable products

The new biofoundry will use gas fermentation, in which microbes convert CO₂, CO, and methane into fuels, chemicals, and materials. The technology is emerging as a key pathway for reducing industrial emissions and enabling circular, climate‑positive solutions. Engineering these specialized microbes is, however, difficult, requiring advanced automation, AI, robotics, gas‑handling and high‑throughput strain‑development tools.

“This partnership brings unique capabilities to Denmark and accelerates our ambition to turn carbon emissions into valuable products. Working with LanzaTech strengthens our ability to drive sustainable innovation with real impact,” says Luuk van der Wielen, Director of BRIGHT.

LanzaTech has spent more than 15 years developing world‑leading synthetic biology capabilities for carbon‑fixing, gas‑fermenting organisms, including the first dedicated biofoundry for these challenging microbes. LanzaTech’s unique biofoundry solution is purpose-built for non-model organisms with highly customized anaerobic and gas-handling capabilities and advanced workflows validated through many years of operation.

“We are delighted to partner with BRIGHT, whose vision, expertise, and commitment to transformative research make them the ideal partner for LanzaTech. This marks a significant milestone in our transformation. By creating a dedicated team that consolidates our biotechnology know-how, we can focus the broader team on our commitment to delivering commercial sustainable aviation fuel and biorefining projects,” says LanzaTech CEO Jennifer Holmgren.

Under the new agreement, a LanzaTech team will develop tailored methods and workflows for BRIGHT’s research missions, provide a non‑exclusive license to relevant IP for tools and biofoundry workflows, and design and install a customized C1 biofoundry at DTU.

 

FACTS

Why this partnership matters

Recent advances in C1 biofoundry design at LanzaTech have created new opportunities to develop production strains more efficiently, enabling conversion of CO, CO₂ and methane off‑gases into valuable fuels, chemicals and materials. Access to these capabilities is currently limited, slowing research and technology development worldwide.

Establishing a next‑generation C1 biofoundry at BRIGHT will close this gap and create a shared platform for researchers, partners and innovation activities in Denmark and across Europe.

A C1 biofoundry specialized in microbes that utilize C1 gases will enable:

  • Faster strain development cycles
    Automation and parallelization allow thousands of microbial designs to be generated and tested at once.
  • Reduced innovation risk
    High‑throughput workflows enable testing many more variants, helping teams fail faster and optimize sooner.
  • Integration of AI‑driven design tools
    Data from large-scale strain screening feeds into models that guide the next design cycle, accelerating the Design–Build–Test–Learn loop.
  • Safe, high‑precision research on challenging organisms
    Working with non-model, often anaerobic microbes — and with flammable or toxic gases — requires specialized equipment and know‑how.

Biofoundry Outside 

Biofoundry Outside. Photo: BRIGHT.

Credit

BRIGHT

About BRIGHT

BRIGHT is a research center at the Technical University of Denmark (DTU) focused on enabling transformative research and innovation for a circular and competitive bioeconomy. Through cutting‑edge science, leading research infrastructure, interdisciplinary collaboration, and strong industry partnerships, BRIGHT develops next‑generation biological solutions for foods, materials, and chemicals.

https://bright.dtu.dk/

About LanzaTech

LanzaTech is a global leader in gas fermentation and carbon recycling. With over 15 years of experience engineering carbon‑fixing microbes and operating the world’s first biofoundry for gas‑fermenting organisms, the company develops technologies that turn waste carbon into sustainable fuels, chemicals, and materials.

https://lanzatech.com/