CD8 T cell clonal expansions & aging: A heterogeneous phenomenon with a common outcome

被引:32
作者
Clambey, Eric T.
Kappler, John W.
Marrack, Philippa
机构
[1] Univ Colorado, Hlth Sci Ctr, Natl Jewish Res & Med Ctr, Integrated Dept Immunol, Denver, CO 80206 USA
[2] Univ Colorado, Hlth Sci Ctr, Natl Jewish Res & Med Ctr, Howard Hughes Med Inst, Denver, CO 80206 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80206 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80206 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Biochem & Mol Genet, Denver, CO 80206 USA
关键词
CD8 memory T cells; CD8 clonal expansion; aging; homeostasis;
D O I
10.1016/j.exger.2006.11.008
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
A highly diverse CD8 T cell repertoire is thought to be critical for maintaining appropriate immune defenses against a variety of pathogens. However, in many aged individuals, the diversity of T cell receptors is significantly reduced by the presence of large, monoclonal expansions of CD8 memory T cells. While ongoing research is focused on understanding the molecular alterations in these expansions, one major hurdle to this goal is the apparent heterogeneity of CD8 clonal expansions, which is apparent even in reductionist systems. In this review, we discuss current evidence that CD8 clonal expansions are a heterogeneous phenomenon, and our evolving understanding of what this heterogeneity tells us about CD8 memory T cell homeostasis and how it is altered in aged individuals. (C) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:407 / 411
页数:5
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