T cell receptor alpha variable 12-2 bias in the immunodominant response to Yellow fever virus.

Détails

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Etat: Serval
Version: Author's accepted manuscript
ID Serval
serval:BIB_47E01B2BD815
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
T cell receptor alpha variable 12-2 bias in the immunodominant response to Yellow fever virus.
Périodique
European journal of immunology
Auteur(s)
Bovay A., Zoete V., Dolton G., Bulek A.M., Cole D.K., Rizkallah P.J., Fuller A., Beck K., Michielin O., Speiser D.E., Sewell A.K., Fuertes Marraco S.A.
ISSN
1521-4141 (Electronic)
ISSN-L
0014-2980
Statut éditorial
Publié
Date de publication
02/2018
Peer-reviewed
Oui
Volume
48
Numéro
2
Pages
258-272
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
The repertoire of human αβ T-cell receptors (TCRs) is generated via somatic recombination of germline gene segments. Despite this enormous variation, certain epitopes can be immunodominant, associated with high frequencies of antigen-specific T cells and/or exhibit bias toward a TCR gene segment. Here, we studied the TCR repertoire of the HLA-A*0201-restricted epitope LLWNGPMAV (hereafter, A2/LLW) from Yellow Fever virus, which generates an immunodominant CD8 <sup>+</sup> T cell response to the highly effective YF-17D vaccine. We discover that these A2/LLW-specific CD8 <sup>+</sup> T cells are highly biased for the TCR α chain TRAV12-2. This bias is already present in A2/LLW-specific naïve T cells before vaccination with YF-17D. Using CD8 <sup>+</sup> T cell clones, we show that TRAV12-2 does not confer a functional advantage on a per cell basis. Molecular modeling indicated that the germline-encoded complementarity determining region (CDR) 1α loop of TRAV12-2 critically contributes to A2/LLW binding, in contrast to the conventional dominant dependence on somatically rearranged CDR3 loops. This germline component of antigen recognition may explain the unusually high precursor frequency, prevalence and immunodominance of T-cell responses specific for the A2/LLW epitope.
Mots-clé
Adaptive Immunity/genetics, CD8-Positive T-Lymphocytes/physiology, Cell Line, Clonal Selection, Antigen-Mediated, Clone Cells, Complementarity Determining Regions/genetics, Cytotoxicity, Immunologic, Epitopes, T-Lymphocyte/metabolism, HLA-A2 Antigen/metabolism, Humans, Immunodominant Epitopes/metabolism, Lymphocyte Activation, Receptors, Antigen, T-Cell, alpha-beta/genetics, T-Cell Antigen Receptor Specificity, Viral Proteins/metabolism, Viral Vaccines/immunology, Yellow Fever/genetics, Yellow Fever/immunology, Yellow fever virus/physiology, Antigen recognition, Germline, T cell receptor Alpha Variable (TRAV)-12-2, T cell receptor bias, Yellow Fever virus
Pubmed
Web of science
Création de la notice
09/10/2017 13:38
Dernière modification de la notice
14/12/2018 7:26
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