Precursor frequency, nonlinear proliferation, and functional maturation of virus-specific CD4+ T cells

被引:67
作者
Whitmire, Jason K. [1 ]
Benning, Nicola [1 ]
Whitton, J. Lindsay [1 ]
机构
[1] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
关键词
D O I
10.4049/jimmunol.176.5.3028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The early events regulating antiviral CD4 responses were tracked using an adoptive transfer model. CD4(+) T cell expansion was nonlinear, with a lengthy lag phase followed by 2 days of explosive proliferation. A small number of naive Ag-specific CD4(+) T cells were found in nonlymphoid tissues and, in the 8 days following infection, the number of activated cells increased in all tissues analyzed, and their effector functions matured. Finally, we show that a naive mouse contains similar to 100 naive CD4(+) precursor cells specific for a single epitope, a precursor frequency of similar to 10(-5), similar to that of naive CD8(+) T cells, indicating that the similar to 50-fold difference in size of the two responses to virus infection is determined by something other than the number of precursor cells.
引用
收藏
页码:3028 / 3036
页数:9
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