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

TitleNaive CD4(+) T cell frequency varies for different epitopes and predicts repertoire diversity and response magnitude.
Publication TypeJournal Article
Year of Publication2007
AuthorsMoon, JJ, H Chu, H, Pepper, M, McSorley, SJ, Jameson, SC, Kedl, RM, Jenkins, MK
JournalImmunity
Volume27
Issue2
Pagination203-13
Date Published2007 Aug
ISSN1074-7613
KeywordsAnimals, CD4-Positive T-Lymphocytes, Epitopes, Genetic Variation, Histocompatibility Antigens Class II, Immunization, Mice, Mice, Mutant Strains, Peptides, Receptors, Antigen, T-Cell
Abstract

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 pMHC 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.

DOI10.1016/j.immuni.2007.07.007
Alternate JournalImmunity
PubMed ID17707129
PubMed Central IDPMC2200089
Grant ListF32 AI063793 / AI / NIAID NIH HHS / United States
F32 AI063793-02 / AI / NIAID NIH HHS / United States