The Role of Naive T Cell Precursor Frequency and Recruitment in Dictating Immune Response Magnitude

被引:223
|
作者
Jenkins, Marc K. [1 ]
Moon, James J. [2 ,3 ,4 ]
机构
[1] Univ Minnesota, Sch Med, Ctr Immunol, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Massachusetts Gen Hosp, Ctr Immunol & Inflammatory Dis, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[4] Massachusetts Gen Hosp, Pulm & Crit Care Unit, Charlestown, MA 02129 USA
来源
JOURNAL OF IMMUNOLOGY | 2012年 / 188卷 / 09期
基金
美国国家卫生研究院;
关键词
EX-VIVO ANALYSIS; MHC CLASS-I; REPERTOIRE DIVERSITY; THYMIC SELECTION; INFLUENZA-VIRUS; ANTIGEN; PEPTIDE; EPITOPE; INFECTION; MICE;
D O I
10.4049/jimmunol.1102661
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances in technology have led to the realization that the populations of naive T cells specific for different foreign peptide:MHC (p:MHC) ligands vary in size. This variability is due, in part, to the fact that certain peptides contain amino acids that engage in particularly favorable interactions with TCRs. In addition, deletion of clones with cross-reactivity for self-p:MHC ligands may reduce the size of some naive populations. In many cases, the magnitude of the immune response to individual p:MHC epitopes correlates with the size of the corresponding naive populations. However, this simple relationship may be complicated by variability in the efficiency of T cell recruitment into the immune response. The knowledge that naive population size can predict immune response magnitude may create opportunities for production of more effective subunit vaccines. The Journal of Immunology, 2012, 188: 4135-4140.
引用
收藏
页码:4135 / 4140
页数:6
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