High frequencies cytomegalovirus pp65495-503-specific CD8+ T cells in healthy young and elderly Chinese donors:: Characterization of their phenotypes and TCR vβ usage

被引:10
作者
He, Xian-Hui
Zha, Qing-Bing
Liu, Yi
Xu, Li-Hui
Chi, Xiao-Yun
机构
[1] Jinan Univ, Coll Life Sci & Technol, Inst Tissue Transplantat & Immunol, Guangzhou 510632, Peoples R China
[2] Jinan Univ, Coll Life Sci & Technol, Inst Bioengn, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
human cytomegalovirus; CD8(+) T cells; HLA-A2; tetramer staining; CD28; CD57; TCR usage;
D O I
10.1007/s10875-006-9035-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human cytomegalovirus (HCMV) is a ubiquitous beta-herpesvirus which persists lifelong after primary infection and can lead to a significant disease in the immunocompromised individuals. CD8(+) T cells are believed to play a crucial role in both the elimination of active infection and maintenance of HCMV latency. Large expansions of CD8(+) T cells specific for a single epitope of HCMV have been well documented in Caucasoid population. To date, no similar study has been performed in Chinese populations. Here we report the characteristics of HCMV-specific CD8(+)T cells in healthy young and elderly Chinese donors using pp65(495-503)-loaded HLA-A*0201 tetramers. Cells were stained with a combination of the tetramers and antibodies for CD28 and CD57 or a panel of TCR V beta and analyzed by three-color flow cytometry. The frequencies of pp65(495-503)-specific T cells within total CD8(+) T cell population were between 0.14 and 6.84% (mean 2.45%) in the young donors and were from 0.33 to 6.89% (mean 1.95%) in the elderly donors, respectively. There was no significant difference between the two groups. The expression of CD28 was decreased whereas CD57 expression was increased in tetramer-negative CD8(+) T cells in the elderly when compared with the young group. However, neither of these changes was found within tetramer-positive cell populations. Moreover, TCR V beta usage within tetramer-positive population was predominated by certain TCR V beta subsets. These results demonstrate that large expansions of HCMV-specific CD8(+) T cells with certain subsets TCR V beta exist both in the healthy young and in the elderly Chinese individuals, which may play a role in the maintenance of virus latency but have potential detrimental influence on the immune responses to other pathogens or vaccinations.
引用
收藏
页码:417 / 429
页数:13
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