Large clonal expansions of human virus-specific memory cytotoxic T lymphocytes within the CD57+ CD28- CD8+ T-cell population

被引:103
|
作者
Weekes, MP [1 ]
Wills, MR [1 ]
Mynard, K [1 ]
Hicks, R [1 ]
Sissons, JGP [1 ]
Carmichael, AJ [1 ]
机构
[1] Univ Cambridge, Dept Med, Sch Clin, Cambridge CB2 2QQ, England
基金
英国惠康基金;
关键词
D O I
10.1046/j.1365-2567.1999.00901.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 proportion of human peripheral blood CD8(+) T cells that are CD57(+) CD28(-) is low at birth but increases with age and in individuals infected with human cytomegalovirus (HCMV) or human immunodeficiency virus (HIV). These CD57(+) CD28(-) CD8(+) T cells contain large oligoclonal T-cell expansions whose antigen specificity is unknown. We identified clonal expansions of virus-specific memory cytotoxic T-lymphocyte precursors (CTLp) in both healthy carriers of HCMV and in asymptomatic HIV-infected subjects. In each subject, from the T-cell receptor (TCR) beta-chain hypervariable sequence of each immunodominant CTL clone, we designed complementary oligonucleotide probes to quantify the size and phenotypic segregation of individual virus-specific CTL clones in highly purified populations of peripheral blood CD8(+) T cells. We found large clonal expansions of virus-specific CTL clonotypes in CD57(+) CD28(-) CD8(+) T cells. Using limiting dilution analysis, we found functional peptide-specific CTLp at high frequency in CD57(+) CD28(-) cells. Thus, memory CTL specific for persistent Viruses account for many oligoclonal expansions within CD57(+) CD28(-) CD8(+) T cells.
引用
收藏
页码:443 / 449
页数:7
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