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Lineage relationship and protective immunity of memory CD8 T cell subsets
被引:1495
作者:

Wherry, EJ
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机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

Teichgräber, V
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机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

Becker, TC
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h-index: 0
机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

Masopust, D
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h-index: 0
机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

Kaech, SM
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机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

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von Andrian, UH
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机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA

Ahmed, R
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机构:
Emory Univ, Dept Biol, Atlanta, GA 30322 USA Emory Univ, Dept Biol, Atlanta, GA 30322 USA
机构:
[1] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[4] Harvard Univ, Sch Med, Ctr Blood Res, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词:
D O I:
10.1038/ni889
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Memory CD8 T cells can be divided into two subsets, central (T-CM) and effector (T-EM), but their lineage relationships and their ability to persist and confer protective immunity are not well understood. Our results show that T-CM have a greater capacity than T-EM to persist in vivo and are more efficient in mediating protective immunity because of their increased proliferative potential. We also demonstrate that, following antigen clearance, T-EM convert to T-CM and that the duration of this differentiation is programmed within the first week after immunization. We propose that T-CM and T-EM do not necessarily represent distinct subsets, but are part of a continuum in a linear naive effector --> T-EM --> T-CM differentiation pathway.
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页码:225 / 234
页数:10
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