Expert concerns temper promise of CAR T therapy for aging gut

A Cold Spring Harbor Laboratory study demonstrated CAR T-cell therapy can reverse age-related intestinal decline in mice by targeting senescent cells. While promising, experts caution on safety risks, off-target effects, dosing, and costs for human use.

Cold Spring Harbor Laboratory researchers, led by Semir Beyaz and Corina Amor, engineered CAR T-cells to target uPAR—a marker of senescent cells accumulating with age. In older mice, the therapy restored youthful stem cell-driven renewal of the gut lining (which turns over every 3-5 days), improved barrier integrity, and reduced inflammation, as detailed in initial reports.

"We didn’t just stop the ageing process, but also observed a reversal," said Amor. Beyaz noted: "The decline... is a deficit in the fitness of the stem cells," which the therapy addressed.

Experts praise the potential to mitigate age-related gut issues like infections, damage, and cancer risk (Tuomas Tammela, Memorial Sloan Kettering). However, challenges loom: uPAR appears on some healthy tissues, risking unintended effects elsewhere (Jesse Poganik, Harvard Medical School). Safety, dosing, and human efficacy remain unproven. The therapy's complexity and cost make routine use unlikely soon (Joana Neves, King’s College London).

With no existing treatments for faltering gut regeneration, this advances anti-aging research. Full study: Nature Aging (DOI: 10.1038/s43587-025-01022-w).

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Illustration of UBC scientists in a lab generating helper T cells from stem cells by tuning Notch signaling, advancing immune therapies.
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UBC researchers show how to reliably generate helper T cells from stem cells by tuning Notch signaling

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Scientists at the University of British Columbia report a method to consistently produce human helper T cells from pluripotent stem cells by carefully adjusting the timing of a developmental signal known as Notch. The work, published in Cell Stem Cell, is positioned as a step toward scalable “off-the-shelf” immune-cell therapies for cancer and other diseases.

Cold Spring Harbor Laboratory researchers report that engineered anti-uPAR CAR T cells cleared senescence-linked cells in mice, improving intestinal regeneration, reducing inflammation and strengthening gut barrier function. The approach also aided recovery from radiation-related intestinal injury and showed regenerative signals in experiments using human intestinal and colorectal cells, raising the possibility of future clinical trials.

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Researchers are exploring CAR T-cell therapy to slow the advancement of amyotrophic lateral sclerosis (ALS) by targeting overactive immune cells in the brain. The approach aims to reduce neuron damage without curing the disease. Early studies suggest potential benefits for other neurodegenerative conditions as well.

Scientists at University College London and Great Ormond Street Hospital have developed a base-edited therapy called BE-CAR7 that uses universal CAR T-cells to treat relapsed or refractory T-cell acute lymphoblastic leukemia. Early trial results published in the New England Journal of Medicine and presented at the American Society of Hematology Annual Meeting indicate deep remissions in most patients, including those who did not respond to standard treatments, by tackling long-standing challenges in T-cell–based therapies.

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Researchers at KAIST have developed an injection that transforms immune cells within tumors into active cancer-killing agents, bypassing the need for complex lab procedures. The method uses lipid nanoparticles to deliver instructions directly to macrophages, enabling them to recognize and attack cancer cells while boosting broader immune responses. In animal tests, the approach significantly slowed tumor growth in melanoma models.

Researchers report that small doses of the antibiotic cephaloridine can prompt certain gut bacteria to increase production of colanic acid, a microbial polysaccharide previously tied to longer lifespan in laboratory animals. In experiments, treated roundworms lived longer and mice showed shifts in cholesterol or insulin measures associated with aging, with the team arguing the approach works by acting in the gut rather than throughout the body.

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Researchers at Memorial Sloan Kettering Cancer Center report that colorectal tumors can contain two major subtypes of regulatory T cells with opposing effects—one associated with restraining tumor growth and another linked to suppressing anti-tumor immunity. The work, published in Immunity, helps explain why higher overall levels of these immune cells have been tied to better outcomes in colorectal cancer and suggests a potential strategy for more selective Treg-targeted therapies.

 

 

 

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