Abstract
Although DNA damage is a common cellular event, T cells experience significant genotoxic stresses because of rapid antigen-stimulated expansion and their presence in various nonlymphoid microenvironments. In addition to the well-established link between genomic instability and malignancy, recent genomic studies have uncovered a substantial mutational burden in nonmalignant T cells in both normal aging and disease contexts. Furthermore, genomic damage in T cells is accelerated in autoimmune diseases and in older individuals because of both intrinsic and extrinsic factors. This review highlights the different genotoxic stressors affecting T cells and the detrimental effects of persistent DNA damage and identifies the most critical knowledge gaps.
Original language | English |
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Journal | Trends in Immunology |
DOIs | |
State | Accepted/In press - 2025 |
Keywords
- DNA damage
- aging
- autoimmune
- cancer immunotherapy
- immunosenescence
- senescence
- tumor microenvironment
All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Immunology