Large numbers of dysfunctional CD8+ T lymphocytes bearing receptors for a single dominant CMV epitope in the very old

被引:179
作者
Qin, OY
Wagner, WM
Wikby, A
Walter, S
Aubert, G
Dodi, AI
Travers, P
Pawelec, G
机构
[1] Univ Tubingen, Sect Transplantat Immunol & Immunohematol, Tuebingen Ageing & Tumour Immunol Grp, Tubingen, Germany
[2] Jonkoping Univ, Sch Hlth Sci, Dept Nat Sci & Biomed, Jonkoping, Sweden
[3] Univ Tubingen, Dept Immunol, Tubingen, Germany
[4] UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London, England
关键词
ageing; T cell; tetramer; cytomegalovirus; ELISPOT;
D O I
10.1023/A:1024580531705
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Longitudinal studies suggest that a set of immune parameters including high percentages of peripheral CD8(+), CD28(-), CD57(+) T lymphocytes, low CD4 and B cell counts, and poor T cell proliferative responses to mitogens is associated with decreased remaining longevity in the free-living very elderly (> 85 years). This combination of immune parameters was also significantly associated with an inverted CD4/CD8 ratio and cytomegalovirus seropositivity. Here, using tetramer technology, we show markedly increased numbers of CD8(+) T cells bearing receptors for one single CMV epitope in the very elderly. Moreover, the fraction of these tetramer-reactive cells secreting interferon-gamma after specific antigenic stimulation was significantly lower in the old than in the young, as was the percentage of CD28- positive cells in this population. Therefore, we conclude that marked expansions of CMV-specific CD8(+) T cells have occurred and that the obsession of a large fraction of the entire CD8(+) T cell subset with one single viral epitope may contribute to the increased incidence of infectious disease in the elderly by shrinking the T cell repertoire available for responses to other antigens.
引用
收藏
页码:247 / 257
页数:11
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