Journal article

A shared TCR bias toward an immunogenic EBV epitope dominates in HLA-B*07: 02-Expressing individuals

LC Rowntree, THO Nguyen, C Farenc, H Halim, L Hensen, J Rossjohn, TC Kotsimbos, AW Purcell, K Kedzierska, S Gras, NA Mifsud

Journal of Immunology | AMER ASSOC IMMUNOLOGISTS | Published : 2020

Abstract

EBV is one of the most common viruses found in humans and is prototypic of a persistent viral infection characterized by periods of latency. Across many HLA class I molecules, the latent-specific CD8+ T cell response is focused on epitopes derived from the EBNA-3 protein family. In the case of HLA-B*07:02 restriction, a highly frequent class I allele, the T cell response is dominated by an epitope spanning residues 379-387 of EBNA-3 (RPPIFIRRL [EBVRPP]). However, little is known about either the TCR repertoire specific for this epitope or the molecular basis for this observed immunodominance. The EBVRPP CD8+ T cell response was common among both EBV-seropositive HLA-B*07:02+ healthy and immu..

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