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IgG4自身抗体在地方性落叶型天疱疮(fogo selvagem)中的致病作用。

The pathogenic effect of IgG4 autoantibodies in endemic pemphigus foliaceus (fogo selvagem).

作者信息

Rock B, Martins C R, Theofilopoulos A N, Balderas R S, Anhalt G J, Labib R S, Futamura S, Rivitti E A, Diaz L A

机构信息

Department of Dermatology, Johns Hopkins University, Baltimore.

出版信息

N Engl J Med. 1989 Jun 1;320(22):1463-9. doi: 10.1056/NEJM198906013202206.

Abstract

Endemic pemphigus foliaceus, or fogo selvagem, is an autoimmune blistering skin disease caused by IgG autoantibodies to a desmosome-associated glycoprotein. We studied the IgG subclasses with autoantibody activity in serum from 29 patients with active disease and in the skin lesions of 18 patients by immunofluorescence, using IgG-subclass-specific monoclonal antibodies. The predominant disease autoantibodies present in all patients were of the IgG4 subclass. IgG1 and IgG2 autoantibodies were detected in low titer in the 29 patients: IgG1 in 23 patients and IgG2 in 9. IgG3 autoantibodies were not detected in the serum of any patient. Direct immunofluorescence testing of skin lesions showed a preferential deposition of IgG4 on the keratinocyte surface. The pathogenic effect of IgG4 was demonstrated by the passive transfer of fractions containing IgG4 autoantibodies from the patients to neonatal BALB/c mice. The disease of the patients was reproduced clinically, histologically, and immunologically in these animals. Only IgG4 autoantibodies were detected by direct immunofluorescence, bound to the epidermis in the lesions of the mice, and by immunoelectron microscopy at the keratinocyte surface. IgG4 has previously been reported to be a blocking or protective antibody because it has poor effector functions in vitro, as compared with the other IgG subclasses. The finding that it is the pathogenic autoantibody in fogo selvagem raises the possibility that it may also be important in other autoimmune disease.

摘要

地方性落叶型天疱疮,即巴西落叶型天疱疮,是一种自身免疫性水疱性皮肤病,由针对桥粒相关糖蛋白的IgG自身抗体引起。我们使用IgG亚类特异性单克隆抗体,通过免疫荧光法研究了29例活动性疾病患者血清和18例患者皮肤病变中具有自身抗体活性的IgG亚类。所有患者中存在的主要疾病自身抗体均为IgG4亚类。在29例患者中检测到低滴度的IgG1和IgG2自身抗体:23例患者中有IgG1,9例患者中有IgG2。在任何患者的血清中均未检测到IgG3自身抗体。皮肤病变的直接免疫荧光检测显示IgG4在角质形成细胞表面优先沉积。通过将含有患者IgG4自身抗体的组分被动转移到新生BALB/c小鼠体内,证明了IgG4的致病作用。在这些动物中,临床、组织学和免疫学上再现了患者的疾病。通过直接免疫荧光法在小鼠病变的表皮中检测到仅与IgG4自身抗体结合,并且通过免疫电子显微镜在角质形成细胞表面检测到。此前有报道称IgG4是一种封闭性或保护性抗体,因为与其他IgG亚类相比,它在体外的效应功能较差。它是巴西落叶型天疱疮中的致病性自身抗体这一发现增加了它在其他自身免疫性疾病中也可能很重要的可能性。

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