Back to Search Start Over

Dominant HLA-mediated protection from the risk of autoimmune renal disease is conferred by antigen-specific regulatory T cells.

Authors :
Huynh M.
Holt S.G.
Coates P.T.
Gregersen J.W.
Purcell A.W.
La Gruta N.L.
Reid H.H.
Rossjohn J.
Kitching A.R.
Holdsworth S.R.
Ooi J.D.
Petersen J.
Tan Y.H.
Willett Z.J.
Ramarathinam S.H.
Eggenhuizen P.J.
Loh K.L.
Watson K.A.
Gan P.Y.
Alikhan M.A.
Dudek N.L.
Handel A.
Hudson B.G.
Fugger L.
Power D.A.
Huynh M.
Holt S.G.
Coates P.T.
Gregersen J.W.
Purcell A.W.
La Gruta N.L.
Reid H.H.
Rossjohn J.
Kitching A.R.
Holdsworth S.R.
Ooi J.D.
Petersen J.
Tan Y.H.
Willett Z.J.
Ramarathinam S.H.
Eggenhuizen P.J.
Loh K.L.
Watson K.A.
Gan P.Y.
Alikhan M.A.
Dudek N.L.
Handel A.
Hudson B.G.
Fugger L.
Power D.A.
Publication Year :
2017

Abstract

Aim: To use Goodpasture's disease (GPD), a classical form of HLA-linked autoimmunity, to define the mechanism of HLA-mediated risk, and dominant protection from risk of disease. Background(s): The mechanisms underpinning HLA-mediated susceptibility to, and protection from autoimmune diseases are unknown. GPD is HLAlinked and characterized by an immunodominant CD4+ self-epitope derived from the alpha3 chain of Type IV collagen (alpha3135-145). Method(s): HLA-DR transgenic mice, cells from HLA-typed healthy humans and from patients with GPD were used, with HLA-DR-alpha3135-145 tetramers, Xray crystallography, and in vivo/in vitro models of autoimmunity. Result(s): Autoreactive alpha3135-145-specific T cells clonally expanded in GPD patients. In alpha3135-145-immunized HLA-DR15 transgenic mice with GPD, alpha3135-145-specific T cells infiltrated the kidney. Structurally, HLA-DR15 and HLA-DR1 presented alpha3135-145 in different binding registers, resulting in differential T cell receptor (TCR) usage. HLA-DR15-alpha3135-145 tetramer+ CD4+ T cells in disease susceptible HLA-DR15 transgenic mice exhibited a conventional phenotype (Tconv), secreting pro-inflammatory cytokines. In contrast, HLA-DR1-alpha3135-145 tetramer+ cells in disease resistant HLA-DR1 and HLADR15/ DR1 transgenic mice were largely CD4+Foxp3+ regulatory T cells (Tregs) expressing tolerogenic cytokines. In HLA-DR15/DR1 transgenic mice, HLA-DR1-alpha3135-145 specific Tregs conferred protection to alpha3135-145-specific autoimmunity and protected from GPD (alpha3135-145-immunized, Treg intact vs Treg depleted: segmental necrosis 0+/-0 vs 50+/-13% P<0.01, serum urea 9+/-1 vs 31+/-10 P<0.001). HLA-DR15+ and HLA-DR1+ healthy human donors displayed altered alpha3135-145-specific TCRs, with HLA-DR15-alpha3135-145 tetramer+ Foxp3- Tconv and HLA-DR1-alpha3135-145 tetramer+ Foxp3+CD25hiCD127lo Treg dominant phenotypes (alpha3135-145 tetramer+ Treg:Tconv ratios: DR15 0.04+/-0.00, DR1 9.61+/-1.79, P<0.001). Conclusio

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1305133521
Document Type :
Electronic Resource