Numbers and odds: TCR repertoire size and its age changes impacting on T cell functions

被引:8
作者
Weng, Nan -ping [1 ]
机构
[1] NIA, Lab Mol Biol & Immunol, NIH, Baltimore, MD 20814 USA
关键词
alpha beta TCR; TCR repertoire; Diversity index; Species richness; Aging; CD4+T cells; CD8+T cells; IAV; CMV; RECEPTOR ALPHA; DIVERSITY; SEQUENCE; DIFFERENTIATION; SEROPOSITIVITY; POPULATION; GENERATION; DISTINCT; CD4(+); OUTPUT;
D O I
10.1016/j.smim.2023.101810
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A vast array of alpha beta T cell receptors (TCRs) is generated during T cell development in the thymus through V(D)J recombination, which involves the rearrangement of multiple V, D, and J genes and the pairing of alpha and beta chains. These diverse TCRs provide protection to the human body against a multitude of foreign pathogens and internal cancer cells. The entirety of TCRs present in an individual's T cells is referred to as the TCR repertoire. Despite an estimated 4 x 10(11) T cells in the adult human body, the lower bound estimate for the TCR repertoire is 3.8 x 10(8). While the number of circulating T cells may slightly decrease with age, the changes in the diversity of the TCR repertoire is more apparent. Here, I review recent advancements in TCR repertoire studies, the methods used to measure it, how richness and diversity change as humans age, and some of the known consequences associated with these changes.
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页数:7
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