Naive CD4+ T cell frequency varies for different epitopes and predicts repertoire diversity and response magnitude

被引:755
作者
Moon, James J.
Chu, H. Hamlet
Pepper, Marion
McSorley, Stephen J.
Jameson, Stephen C.
Kedl, Ross M.
Jenkins, Marc K. [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Sch Med, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[5] Univ Colorado, Hlth Sci Ctr, Integrated Dept Immunol, Denver, CO 80206 USA
关键词
D O I
10.1016/j.immuni.2007.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell-mediated immunity stems from the proliferation of naive T lymphocytes expressing T cell antigen receptors (TCRs) specific for foreign peptides bound to host major histocompatibility complex (MHC) molecules. Because of the tremendous diversity of the T cell repertoire, naive T cells specific for any one peptide:MHC complex (pMHC) are extremely rare. Thus, it is not known how many naive T cells of any given pMlHC specificity exist in the body or how that number influences the immune response. By using soluble pMHC class II (pMHCII) tetramers and magnetic bead enrichment, we found that three different pMHCII-specific naive CD4(+) T cell populations vary in frequency from 20 to 200 cells per mouse. Moreover, naive population size predicted the size and TCR diversity of the primary CD4(+) T cell response after immunization with relevant peptide. Thus, variation in naive T cell frequencies can explain why some peptides are stronger immunogens than others.
引用
收藏
页码:203 / 213
页数:11
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