共 46 条
CD4+ T cells are required for the maintenance, not programming, of memory CD8+ T cells after acute infection
被引:476
作者:

Sun, JC
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机构: Univ Washington, Dept Immunol, Seattle, WA 98195 USA

Williams, MA
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h-index: 0
机构: Univ Washington, Dept Immunol, Seattle, WA 98195 USA

Bevan, MJ
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h-index: 0
机构:
Univ Washington, Dept Immunol, Seattle, WA 98195 USA Univ Washington, Dept Immunol, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词:
D O I:
10.1038/ni1105
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Immunization in the absence of CD4(+) T cell help results in defective CD8(+) T cell memory, deficient recall responses and diminished protective immunity. Here we investigated at what stage during the immune response to pathogen CD4(+) T cells are essential in the promotion of functional CD8(+) T cell memory. Memory CD8(+) T cell numbers decreased gradually in the absence of CD4(+) T cells despite the presence of similar numbers of memory cell precursors at the peak of the effector phase. Adoptive transfer of effector or memory CD8(+) T cells into wild-type or CD4(+) T cell-deficient mice demonstrated that the presence of CD4(+) T cells was important only after, not during, the early CD8(+) T cell programming phase. In the absence of CD4(+) T cells, memory CD8(+) T cells became functionally impaired and decreased in quantity over time. We conclude that in the context of an acute infection, CD4(+) T cells are required only during the maintenance phase of long-lived memory CD8(+) T cells.
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页码:927 / 933
页数:7
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