Heterogeneous Differentiation Patterns of Individual CD8+ T Cells

被引:268
作者
Gerlach, Carmen [1 ]
Rohr, Jan C. [1 ,2 ,3 ]
Perie, Leila [1 ,4 ]
van Rooij, Nienke [1 ]
van Heijst, Jeroen W. J. [1 ]
Velds, Arno [5 ]
Urbanus, Jos [1 ]
Naik, Shalin H. [1 ]
Jacobs, Heinz [6 ]
Beltman, Joost B. [1 ,4 ]
de Boer, Rob J. [4 ]
Schumacher, Ton N. M. [1 ]
机构
[1] Netherlands Canc Inst, Div Immunol, NL-1066 CX Amsterdam, Netherlands
[2] Univ Med Ctr Freiburg, Ctr Chron Immunodeficiency CCI, Freiburg, Germany
[3] Univ Freiburg, D-79106 Freiburg, Germany
[4] Univ Utrecht, Utrecht, Netherlands
[5] Netherlands Canc Inst, Cent Genom Facil, NL-1066 CX Amsterdam, Netherlands
[6] Netherlands Canc Inst, Div Biol Stress Responses, NL-1066 CX Amsterdam, Netherlands
基金
欧洲研究理事会;
关键词
INFECTION; EFFECTOR; FATES; ACTIVATION; PRECURSOR; DIVISION; SUBSETS;
D O I
10.1126/science.1235487
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Upon infection, antigen-specific CD8(+) T lymphocyte responses display a highly reproducible pattern of expansion and contraction that is thought to reflect a uniform behavior of individual cells. We tracked the progeny of individual mouse CD8(+) T cells by in vivo lineage tracing and demonstrated that, even for T cells bearing identical T cell receptors, both clonal expansion and differentiation patterns are heterogeneous. As a consequence, individual naive T lymphocytes contributed differentially to short-and long-term protection, as revealed by participation of their progeny during primary versus recall infections. The discordance in fate of individual naive T cells argues against asymmetric division as a singular driver of CD8(+) T cell heterogeneity and demonstrates that reproducibility of CD8(+) T cell responses is achieved through population averaging.
引用
收藏
页码:635 / 639
页数:5
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