Benefit delayed immunosenescence by regulating CD4<sup>+</sup>T cells: A promising therapeutic target for aging-related diseases.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 39155409.
- Also identified by DOI 10.1111/acel.14317 and PMC identifier 11464113.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
CD4<sup>+</sup>T cells play a notable role in immune protection at different stages of life. During aging, the interaction between the body's internal and external environment and CD4<sup>+</sup>T cells results in a series of changes in the CD4<sup>+</sup>T cells pool making it involved in immunosenescence. Many studies have extensively examined the subsets and functionality of CD4<sup>+</sup>T cells within the immune system, highlighted their pivotal role in disease pathogenesis, progression, and therapeutic interventions. However, the underlying mechanism of CD4<sup>+</sup>T cells senescence and its intricate association with diseases remains to be elucidated and comprehensively understood. By summarizing the immunosenescent progress and network of CD4<sup>+</sup>T cell subsets, we reveal the crucial role of CD4<sup>+</sup>T cells in the occurrence and development of age-related diseases. Furthermore, we provide new insights and theoretical foundations for diseases targeting CD4<sup>+</sup>T cell subsets aging as a treatment focus, offering novel approaches for therapy, especially in infections, cancers, autoimmune diseases, and other diseases in the elderly.
Medical subject headings
- Immunosenescence
- CD4-Positive T-Lymphocytes
- Aging