Oligoclonal expansions in the CD8+CD28- T cells largely explain the shorter telomeres detected in this subset:: Analysis by flow FISH

被引:49
作者
Batliwalla, FM
Rufer, N
Lansdorp, PM
Gregersen, PK
机构
[1] N Shore Univ Hosp, Dept Med, Div Biol & Human Genet, Manhasset, NY 11050 USA
[2] Univ Geneva, Div Immunol & Allergol, Geneva, Switzerland
[3] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[4] Univ British Columbia, British Columbia Canc Res Ctr, Terry Fox Lab, Vancouver, BC, Canada
关键词
human CD8(+) CD28(-) T cells; oligoclonality; telomere length; cytokines; flow FISH;
D O I
10.1016/S0198-8859(00)00157-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously reported that CD8(+)CD28(-) T cells have relatively shorter telomeres compared with CD8(+)CD28(+) T cells. Oligoclonal expansion is a common feature of CD8(+) T cells in human peripheral blood, and these expansions predominantly occur in the CD57(+)/CD28(-) population. We studied che telomere length in subsets of CD8(+) T cells using quantitative fluorescence in situ hybridization and flow cytometry (flow FISH). Our results confirm that CD8(+)CD28(-) cells have shorter telomeres as compared with their CD28(+) counterpart cells. In addition, the oligoclonally expanded cells within the CD8+CD28- T cell subset generally have even shorter telomeres than the CD28(-) subset as a whole. We conclude that the presence of clonal expansions in the CD8(+)CD28(-) T cell population largely explain the shorter telomeres in this subset. These clonally expanded CD8(+)CD28(-) T cells generally have characteristics of terminally differentiated effector cells. Nevertheless, there is considerable individual variation in the degree of telomere shortening in these cells, which may reflect host genetic factors as well as the type and timing of the antigenic exposure. (C) American Society for Histocompatibility and Immunogenetics, 2000. published by Elsevier Science Inc.
引用
收藏
页码:951 / 958
页数:8
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