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T Cell Epitope Mimicry between Sjögren’s Syndrome Antigen A (SSA)/Ro60 and Oral Gut Skin and Vaginal Bacteria.

机译:Sjögren综合征抗原A(SSA)/ Ro60与口腔肠道皮肤和阴道细菌之间的T细胞抗原决定簇。

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摘要

This study was undertaken to test the hypothesis that Sjogren’s syndrome Antigen A (SSA)/Ro60-reactive T cells are activated by peptides originating from oral and gut bacteria. T cell hybridomas generated from HLA-DR3 transgenic mice recognized 3 regions on Ro60, with core epitopes mapped to amino acids 228-238, 246-256 and 371-381. BLAST analysis identified several mimicry peptides, originating from human oral, intestinal, skin and vaginal bacteria, as well as environmental bacteria. Amongst these, a peptide from the von Willebrand factor type A domain protein (vWFA) from the oral microbe Capnocytphaga ochracea was the most potent activator. Further, Ro60-reactive T cells were activated by recombinant vWFA protein and whole E. coli expressing this protein. These results demonstrate that peptides derived from normal human microbiota can activate Ro60-reactive T cells. Thus, immune responses to commensal microbiota and opportunistic pathogens should be explored as potential triggers for initiating autoimmunity in SLE and Sjögren’s syndrome.
机译:这项研究的目的是检验干燥口腔和肠道细菌产生的肽激活Sjogren综合征抗原A(SSA)/ Ro60反应性T细胞的假说。从HLA-DR3转基因小鼠产生的T细胞杂交瘤识别Ro60上的3个区域,核心表位定位于氨基酸228-238、246-256和371-381。 BLAST分析鉴定了几种模仿肽,其源自人口腔,肠,皮肤和阴道细菌以及环境细菌。其中,来自口腔微生物Capnocytphaga ochracea的von Willebrand因子A域蛋白(vWFA)的肽是最有效的激活剂。此外,Ro60反应性T细胞被重组vWFA蛋白和表达该蛋白的整个大肠杆菌激活。这些结果证明,源自正常人微生物群的肽可以激活Ro60反应性T细胞。因此,应该探索对共生微生物和机会性病原体的免疫反应,作为引发SLE和Sjögren综合征自身免疫的潜在诱因。

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