Gain and Loss of T Cell Subsets in Old Age-Age-Related Reshaping of the T Cell Repertoire

被引:130
作者
Arnold, Christoph R. [1 ]
Wolf, Juliane [1 ]
Brunner, Stefan [1 ]
Herndler-Brandstetter, Dietmar [1 ]
Grubeck-Loebenstein, Beatrix [1 ]
机构
[1] Austrian Acad Sci, Div Immunol, Inst Biomed Aging Res, A-6020 Innsbruck, Austria
关键词
Immunosenescence; T cells; aging; human; CYTOMEGALOVIRUS-SPECIFIC CD4(+); HUMAN-IMMUNODEFICIENCY-VIRUS; HEMATOPOIETIC STEM-CELLS; CHRONIC VIRAL-INFECTION; IMMUNE-RESPONSES; EFFECTOR MEMORY; ELDERLY PERSONS; HOMEOSTATIC PROLIFERATION; LYMPHOCYTE DEVELOPMENT; ENDOTHELIAL-CELLS;
D O I
10.1007/s10875-010-9499-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system is affected by the aging process and undergoes significant age-related changes, termed immunosenescence. Different T cell subsets are affected by this process. Alterations within the bone marrow and thymus lead to a shift in the composition of the T cell repertoire from na < ve to antigen-experienced T cells, thereby compromising the diversity of the T cell pool. Additional infection with latent pathogens such as cytomegalovirus aggravates this process. In this review, we focus on the major age-related changes that occur in the na < ve and the antigen-experienced T cell population. We discuss the mechanisms responsible for the generation and maintenance of these subsets and how age-related changes can be delayed or prevented by clinical interventions.
引用
收藏
页码:137 / 146
页数:10
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