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[自身抗体产生的新机制:MHC II类分子对错误折叠蛋白的抗原呈递]

[A new mechanism of autoantibody production: antigen presentation of misfolded protein by MHC class II].

作者信息

Ohmura Koichiro, Hiwa Ryosuke, Arase Hisashi

机构信息

Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 2014;37(6):462-7. doi: 10.2177/jsci.37.462.

Abstract

Recently a new pathogenic mechanism for autoantibody production was proposed. Misfolded proteins bind to MHC class II in the endoplasmic reticulum and are processed to be presented at the cell surface. Misfolded proteins are not trimmed to peptides, but are presented as they are together with MHC class II molecules. Such misfolded protein/MHC class II complex can stimulate B cells, but not T cells, and will induce autoantibody production. One of such examples is the case of IgG heavy chain (IgGH). HLA class II can bind IgGH and presents it to the cell surface. Such IgGH/HLA class II complex can be recognized by rheumatoid factor. Surprisingly, RA susceptible HLA class II alleles can present IgGH efficiently, but RA resistant HLA class II alleles cannot. Therefore susceptibility to certain autoimmune diseases may be determined by the affinity of misfolded autoantigens to certain HLA class II alleles. Such new autoimmune mechanisms may explain the unexplained autoantibody production mechanisms.

摘要

最近提出了一种自身抗体产生的新致病机制。错误折叠的蛋白质在内质网中与II类主要组织相容性复合体(MHC)结合,并被加工后呈递至细胞表面。错误折叠的蛋白质不会被修剪成肽段,而是与II类MHC分子一起原样呈递。这种错误折叠的蛋白质/II类MHC复合体可刺激B细胞,但不能刺激T细胞,并会诱导自身抗体产生。其中一个例子就是IgG重链(IgGH)的情况。II类人类白细胞抗原(HLA)可结合IgGH并将其呈递至细胞表面。这种IgGH/II类HLA复合体可被类风湿因子识别。令人惊讶的是,对类风湿关节炎(RA)易感的II类HLA等位基因能够有效地呈递IgGH,而对RA有抗性的II类HLA等位基因则不能。因此,对某些自身免疫性疾病的易感性可能由错误折叠的自身抗原与某些II类HLA等位基因的亲和力决定。这种新的自身免疫机制可能解释了无法解释的自身抗体产生机制。

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