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Type: Journal article
Title: Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cells
Author: Ooi, J.
Petersen, J.
Tan, Y.
Huynh, M.
Willett, Z.
Ramarathinam, S.
Eggenhuizen, P.
Loh, K.
Watson, K.
Gan, P.
Alikhan, M.
Dudek, N.
Handel, A.
Hudson, B.
Fugger, L.
Power, D.
Holt, S.
Coates, P.
Gregersen, J.
Purcell, A.
et al.
Citation: Nature, 2017; 545(7653):243-247
Publisher: Nature Publishing Group
Issue Date: 2017
ISSN: 0028-0836
Statement of
Joshua D. Ooi, Jan Petersen, Yu H. Tan, Megan Huynh, Zoe J. Willett, Sri H. Ramarathinam, Peter J. Eggenhuizen, Khai L. Loh, Katherine A. Watson, Poh Y. Gan, Maliha A. Alikhan, Nadine L. Dudek, Andreas Handel, Billy G. Hudson, Lars Fugger, David A. Power, Stephen G. Holt, P. Toby Coates, Jon W. Gregersen, Anthony W. Purcell, Stephen R. Holdsworth, Nicole L. La Gruta, Hugh H. Reid, Jamie Rossjohn and A. Richard Kitching
Abstract: Susceptibility and protection against human autoimmune diseases, including type I diabetes, multiple sclerosis, and Goodpasture disease, is associated with particular human leukocyte antigen (HLA) alleles. However, the mechanisms underpinning such HLA-mediated effects on self-tolerance remain unclear. Here we investigate the molecular mechanism of Goodpasture disease, an HLA-linked autoimmune renal disorder characterized by an immunodominant CD4+ T-cell self-epitope derived from the α3 chain of type IV collagen (α3135-145). While HLA-DR15 confers a markedly increased disease risk, the protective HLA-DR1 allele is dominantly protective in trans with HLA-DR15 (ref. 2). We show that autoreactive α3135-145-specific T cells expand in patients with Goodpasture disease and, in α3135-145-immunized HLA-DR15 transgenic mice, α3135-145-specific T cells infiltrate the kidney and mice develop Goodpasture disease. HLA-DR15 and HLA-DR1 exhibit distinct peptide repertoires and binding preferences and present the α3135-145 epitope in different binding registers. HLA-DR15-α3135-145 tetramer+ T cells in HLA-DR15 transgenic mice exhibit a conventional T-cell phenotype (Tconv) that secretes pro-inflammatory cytokines. In contrast, HLA-DR1-α3135-145 tetramer+ T cells in HLA-DR1 and HLA-DR15/DR1 transgenic mice are predominantly CD4+Foxp3+ regulatory T cells (Treg cells) expressing tolerogenic cytokines. HLA-DR1-induced Treg cells confer resistance to disease in HLA-DR15/DR1 transgenic mice. HLA-DR15+ and HLA-DR1+ healthy human donors display altered α3135-145-specific T-cell antigen receptor usage, HLA-DR15-α3135-145 tetramer+ Foxp3- Tconv and HLA-DR1-α3135-145 tetramer+ Foxp3+CD25hiCD127lo Treg dominant phenotypes. Moreover, patients with Goodpasture disease display a clonally expanded α3135-145-specific CD4+ T-cell repertoire. Accordingly, we provide a mechanistic basis for the dominantly protective effect of HLA in autoimmune disease, whereby HLA polymorphism shapes the relative abundance of self-epitope specific Treg cells that leads to protection or causation of autoimmunity.
Keywords: CD4-Positive T-Lymphocytes; Animals; Mice, Transgenic; Humans; Mice; Anti-Glomerular Basement Membrane Disease; Collagen Type IV; HLA-DR1 Antigen; Immunodominant Epitopes; Cytokines; Autoimmunity; Base Sequence; Models, Molecular; Female; Male; T-Lymphocytes, Regulatory; Forkhead Transcription Factors; HLA-DR Serological Subtypes
Description: Letter
Rights: © 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
RMID: 0030072348
DOI: 10.1038/nature22329
Grant ID:
Appears in Collections:Medicine publications

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