The cellular senescence–metabolism axis: emerging insights into T cell dynamics in the context of biological aging
The exponential growth of immunometabolism-related studies in the last 10 years has made it very clear that metabolism is a key player in the effector functions of immune cells. Such is the case in cells with lymphoid origin, as CD4 + and CD8 + T cells undergo a series of metabolic reprogramming steps during their differentiation process, which is associated with a change in their effector characteristics. Only recently have factors such as biological aging and cellular senescence been examined in relation to memory T-cell generation and the metabolic reprogramming that accompanies their differentiation. In this review, we examine the emerging roles of cellular senescence and biological aging in shaping T-cell metabolism and immune function, and how these changes in the T-cell landscape contribute to disease onset. We then discuss recent studies on T-cell metabolic reprogramming to highlight how understanding the impact of senescence on T-cell metabolism may reveal new therapeutic opportunities.
Authors
- Patricia Fitzgerald-Bocarsly
- Luis Garza-Martínez
Institutions
- Rutgers, The State University of New Jersey (US)
- Rutgers Sexual and Reproductive Health and Rights (NL)
Publication Details
- Journal
- Cell Communication and Signaling
- Published
- 2025-12-09
- DOI
- https://doi.org/10.1186/s12964-025-02525-0
- Primary Topic
- Telomeres, Telomerase, and Senescence
- Type
- article
- Field-Weighted Citation Impact
- 0.00