A new study reveals that ageing weakens CAR-T cell therapy by disrupting cellular metabolism. Researchers found that restoring NAD levels can rejuvenate these immune cells in preclinical models. The findings emphasize the need for age-inclusive immunotherapy development. This breakthrough could improve cancer treatment for older patients.
May 21, 2025
Ageing reduces CAR-T cell effectiveness by impairing metabolism, study shows
"CAR-T
cells from older individuals are metabolically impaired and significantly less
effective." – Dr. Helen Carrasco Hope
People's
immune systems deteriorate as they age, making cancer therapies that rely on
immune cells difficult to implement.
Key
Points
1 Ageing lowers NAD levels in CAR-T cells
2 Impaired mitochondria reduce antitumor function
3 NAD boosters restore cell effectiveness
4 Study urges age-inclusive immunotherapy trials
In
a new study, researchers from the University of Lausanne (UNIL), the Lausanne
University Hospital (CHUV), the Geneva University Hospitals (HUG), and the
Ecole Polytechnique Federale de Lausanne (EPFL) show that age-related immune
decline has a measurable impact on CAR-T cell therapy, one of the most advanced
forms of cancer immunotherapy.
CAR-T
therapy works by engineering a patient's T-cells to recognize and destroy
cancer cells. But the study found that CAR-T cells from aged mice had poor
mitochondrial function, lower "stemness", and reduced antitumor
activity. The culprit: a drop in levels of nicotinamide adenine dinucleotide
(NAD), a molecule essential for cellular energy and metabolism of mitochondria.
"CAR-T
cells from older individuals are metabolically impaired and significantly less
effective," said first author Dr. Helen Carrasco Hope. "What's
exciting is that we were able to rejuvenate these aged cells by restoring their
NAD levels--reviving their antitumor function in preclinical models."
"Our
findings strengthen the growing recognition that aging fundamentally reshapes
immune cell function and metabolism," she added. "They highlight the
urgent need to model age more accurately in preclinical studies, so that
therapies are developed with the real-world cancer population in mind--where
most patients are older adults."
The
team used NAD-boosting compounds currently under clinical investigation for
other conditions, demonstrating that this approach is translatable and
potentially applicable in humans. "This is a major step toward
personalized and age-conscious immunotherapy," said senior author Dr.
Nicola Vannini. "By correcting age-related metabolic defects, we could
improve outcomes for a large segment of cancer patients."
The
study adds to a growing body of work showing that age is not just a
chronological number, but a biological factor that can shape therapy response.
The authors call for age to be systematically considered in the development and
evaluation of cell-based immunotherapies.
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