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J Immunol. 2019 May 1;202(9):2558-2569. doi: 10.4049/jimmunol.1801454. Epub 2019 Mar 29.

Epitope Selection for HLA-DQ2 Presentation: Implications for Celiac Disease and Viral Defense.

Author information

1
Division of Human Gene Therapy, Department of Pediatrics, Stanford University, Stanford, CA 94305.
2
Program in Immunology, Stanford University, Stanford, CA 94305.
3
Centre for Immune Regulation, Department of Immunology, University of Oslo and Oslo University Hospital, Rikshospitalet, 0372 Oslo, Norway.
4
K.G. Jebsen Coeliac Disease Research Centre, University of Oslo, 0424 Oslo, Norway.
5
Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
6
Department of Medical Oncology, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands.
7
Department of Medicine, University of Washington, Seattle, WA 98195.
8
Department of Laboratory Medicine, University of Washington, Seattle, WA 98195; and.
9
Department of Global Health, University of Washington, Seattle, WA 98195.
10
Division of Human Gene Therapy, Department of Pediatrics, Stanford University, Stanford, CA 94305; mellins@stanford.edu.

Abstract

We have reported that the major histocompatibility molecule HLA-DQ2 (DQA1*05:01/DQB1*02:01) (DQ2) is relatively resistant to HLA-DM (DM), a peptide exchange catalyst for MHC class II. In this study, we analyzed the role of DQ2/DM interaction in the generation of DQ2-restricted gliadin epitopes, relevant to celiac disease, or DQ2-restricted viral epitopes, relevant to host defense. We used paired human APC, differing in DM expression (DMnull versus DMhigh) or differing by expression of wild-type DQ2, versus a DM-susceptible, DQ2 point mutant DQ2α+53G. The APC pairs were compared for their ability to stimulate human CD4+ T cell clones. Despite higher DQ2 levels, DMhigh APC attenuated T cell responses compared with DMnull APC after intracellular generation of four tested gliadin epitopes. DMhigh APC expressing the DQ2α+53G mutant further suppressed these gliadin-mediated responses. The gliadin epitopes were found to have moderate affinity for DQ2, and even lower affinity for the DQ2 mutant, consistent with DM suppression of their presentation. In contrast, DMhigh APC significantly promoted the presentation of DQ2-restricted epitopes derived intracellularly from inactivated HSV type 2, influenza hemagglutinin, and human papillomavirus E7 protein. When extracellular peptide epitopes were used as Ag, the DQ2 surface levels and peptide affinity were the major regulators of T cell responses. The differential effect of DM on stimulation of the two groups of T cell clones implies differences in DQ2 presentation pathways associated with nonpathogen- and pathogen-derived Ags in vivo.

PMID:
30926644
DOI:
10.4049/jimmunol.1801454

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