TY - JOUR
T1 - Prophylactic and long-lasting efficacy of senolytic CAR T cells against age-related metabolic dysfunction
AU - Amor, Corina
AU - Fernández-Maestre, Inés
AU - Chowdhury, Saria
AU - Ho, Yu Jui
AU - Nadella, Sandeep
AU - Graham, Courtenay
AU - Carrasco, Sebastian E.
AU - Nnuji-John, Emmanuella
AU - Feucht, Judith
AU - Hinterleitner, Clemens
AU - Barthet, Valentin J.A.
AU - Boyer, Jacob A.
AU - Mezzadra, Riccardo
AU - Wereski, Matthew G.
AU - Tuveson, David A.
AU - Levine, Ross L.
AU - Jones, Lee W.
AU - Sadelain, Michel
AU - Lowe, Scott W.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/3
Y1 - 2024/3
N2 - Senescent cells, which accumulate in organisms over time, contribute to age-related tissue decline. Genetic ablation of senescent cells can ameliorate various age-related pathologies, including metabolic dysfunction and decreased physical fitness. While small-molecule drugs that eliminate senescent cells (‘senolytics’) partially replicate these phenotypes, they require continuous administration. We have developed a senolytic therapy based on chimeric antigen receptor (CAR) T cells targeting the senescence-associated protein urokinase plasminogen activator receptor (uPAR), and we previously showed these can safely eliminate senescent cells in young animals. We now show that uPAR-positive senescent cells accumulate during aging and that they can be safely targeted with senolytic CAR T cells. Treatment with anti-uPAR CAR T cells improves exercise capacity in physiological aging, and it ameliorates metabolic dysfunction (for example, improving glucose tolerance) in aged mice and in mice on a high-fat diet. Importantly, a single administration of these senolytic CAR T cells is sufficient to achieve long-term therapeutic and preventive effects.
AB - Senescent cells, which accumulate in organisms over time, contribute to age-related tissue decline. Genetic ablation of senescent cells can ameliorate various age-related pathologies, including metabolic dysfunction and decreased physical fitness. While small-molecule drugs that eliminate senescent cells (‘senolytics’) partially replicate these phenotypes, they require continuous administration. We have developed a senolytic therapy based on chimeric antigen receptor (CAR) T cells targeting the senescence-associated protein urokinase plasminogen activator receptor (uPAR), and we previously showed these can safely eliminate senescent cells in young animals. We now show that uPAR-positive senescent cells accumulate during aging and that they can be safely targeted with senolytic CAR T cells. Treatment with anti-uPAR CAR T cells improves exercise capacity in physiological aging, and it ameliorates metabolic dysfunction (for example, improving glucose tolerance) in aged mice and in mice on a high-fat diet. Importantly, a single administration of these senolytic CAR T cells is sufficient to achieve long-term therapeutic and preventive effects.
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U2 - 10.1038/s43587-023-00560-5
DO - 10.1038/s43587-023-00560-5
M3 - Article
C2 - 38267706
AN - SCOPUS:85182978671
SN - 2662-8465
VL - 4
SP - 336
EP - 349
JO - Nature Aging
JF - Nature Aging
IS - 3
ER -