T cell markers recount the course of immunosenescence in healthy individuals and chronic kidney disease

Aging results in substantial changes in almost all cellular subpopulations within the immune system, including functional and phenotypic alterations. T lymphocytes, as the main representative population of cellular immunity, have been extensively studied in terms of modifications and adjustments during aging. Phenotypic alterations are attributed to three main mechanisms; a reduction of naive T cell population with a shift to more differentiated forms, a subsequent oligoclonal expansion of naive T cells characterized by repertoire restriction, and replicative insufficiency after repetitive activation. These changes and the subsequent phenotypic disorders are comprised in the term immunosenescence. Similar changes seem to occur in chronic kidney disease, with T cells of young patients resembling those of healthy older individuals. A broad range of surface markers can be utilized to identify immunosenescent T cells. In this review, we will discuss the most important senescence markers and their potential connection with impaired renal function.

Automated summary

Aging leads to significant changes in almost all cellular subpopulations within the immune system, with T lymphocytes undergoing functional and phenotypic alterations. These changes, known as immunosenescence, are also observed in chronic kidney disease, where T cells of young patients resemble those of healthy older individuals. Various surface markers can be used to identify immunosenescent T cells, which may have potential connections with impaired renal function.