Your browser doesn't support javascript.
loading
DRB4*01:01 Has a Distinct Motif and Presents a Proinsulin Epitope That Is Recognized in Subjects with Type 1 Diabetes.
James, Eddie A; Gillette, Laurel; Durinovic-Bello, Ivana; Speake, Cate; Bondinas, George P; Moustakas, Antonis K; Greenbaum, Carla J; Papadopoulos, George K; Kwok, William W.
Afiliação
  • James EA; Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
  • Gillette L; Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
  • Durinovic-Bello I; Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
  • Speake C; Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
  • Bondinas GP; Laboratory of Biophysics, Biochemistry, Bioprocessing and Bioproducts, Faculty of Agricultural Technology, Technological Educational Institute of Epirus, GR47100 Arta, Greece.
  • Moustakas AK; Department of Food Technology, Technological Educational Institute of Ionian Islands, GR27100 Argostoli, Cephalonia, Greece; and.
  • Greenbaum CJ; Benaroya Research Institute at Virginia Mason, Seattle, WA 98101.
  • Papadopoulos GK; Department of Medicine, University of Washington, Seattle, WA 98195.
  • Kwok WW; Laboratory of Biophysics, Biochemistry, Bioprocessing and Bioproducts, Faculty of Agricultural Technology, Technological Educational Institute of Epirus, GR47100 Arta, Greece.
J Immunol ; 201(12): 3524-3533, 2018 12 15.
Article em En | MEDLINE | ID: mdl-30455401
DRB4*01:01 (DRB4) is a secondary HLA-DR product that is part of the high-risk DR4/DQ8 haplotype that is associated with type 1 diabetes (T1D). DRB4 shares considerable homology with HLA-DR4 alleles that predispose to autoimmunity, including DRB1*04:01 and DRB1*04:04. However, the DRB4 protein sequence includes distinct residues that would be expected to alter the characteristics of its binding pockets. To identify high-affinity peptides that are recognized in the context of DRB4, we used an HLA class II tetramer-based approach to identify epitopes within multiple viral Ags. We applied a similar approach to identify antigenic sequences within glutamic acid decarboxylase 65 and pre-proinsulin that are recognized in the context of DRB4. Seven sequences were immunogenic, eliciting high-affinity T cell responses in DRB4+ subjects. DRB1*04:01-restricted responses toward many of these peptides have been previously described, but responses to a novel pre-proinsulin 9-28 peptide were commonly observed in subjects with T1D. Furthermore, T cells that recognized this peptide in the context of DRB4 were present at significantly higher frequencies in patients with T1D than in healthy controls, implicating this as a disease-relevant specificity that may contribute to the breakdown of ß cell tolerance in genetically susceptible individuals. We then deduced a DRB4 motif and confirmed its key features through structural modeling. This modeling suggested that the core epitope within the pre-proinsulin 9-28 peptide has a somewhat unusual binding motif, with tryptophan in the fourth binding pocket of DRB4, perhaps influencing the availability of this complex for T cell selection.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Proinsulina / Autoantígenos / Linfócitos T / Epitopos de Linfócito T / Diabetes Mellitus Tipo 1 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Proinsulina / Autoantígenos / Linfócitos T / Epitopos de Linfócito T / Diabetes Mellitus Tipo 1 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article