Prophylactic and long-lasting efficacy of senolytic CAR T cells against age-related metabolic dysfunction.
Corina AmorInés Fernández-MaestreSaria ChowdhuryYu-Jui HoSandeep NadellaCourtenay GrahamSebastian E CarrascoEmmanuella Nnuji-JohnJudith FeuchtClemens HinterleitnerValentin J A BarthetJacob A BoyerRiccardo MezzadraMatthew G WereskiDavid A TuvesonRoss L LevineLee W JonesMichel SadelainScott W LowePublished in: Nature aging (2024)
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.
Keyphrases
- induced apoptosis
- cell cycle arrest
- high fat diet
- small molecule
- oxidative stress
- cell death
- endoplasmic reticulum stress
- physical activity
- dna methylation
- dna damage
- type diabetes
- drug delivery
- genome wide
- mouse model
- mesenchymal stem cells
- cancer therapy
- endothelial cells
- skeletal muscle
- stress induced
- pi k akt
- smoking cessation