共 40 条
Cognate CD4+ T cell licensing of dendritic cells in CD8+ T cell immunity
被引:340
作者:

Smith, CM
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机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia

Wilson, NS
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机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia

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Villadangos, JA
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机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia

Carbone, FR
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机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia

Heath, WR
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机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia

Belz, GT
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机构:
Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia
机构:
[1] Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3050, Australia
[2] Walter & Eliza Hall Inst Med Res, Cooperat Res Ctr Vaccine Technol, Melbourne, Vic 3050, Australia
[3] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic 3010, Australia
基金:
英国惠康基金;
关键词:
D O I:
10.1038/ni1129
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Several studies have indicated that CD8(+) T cells require CD4(+) T cell help for memory formation. Evidence suggests that such help can be antigen independent, challenging whether the 'licensing' of dendritic cells (DCs) by CD4(+) T cells is ever required for cytotoxic T lymphocyte (CTL) responses. We show here that help is essential for the generation of CTL immunity to herpes simplex virus 1 and that CD4(+) T cells mediate help in a cognate, antigen-specific way. We provide direct in vivo evidence for DC licensing by helper T cells and show that licensing is rapid and essential for the formation of effector and memory CTLs. In situations in which DCs are poorly licensed by pathogen-derived signals, our findings suggest that CTL immunity may be heavily dependent on cognate DC licensing.
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页码:1143 / 1148
页数:6
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