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抗中性粒细胞胞浆抗体(ANCA)抗独特型抗体与静脉注射免疫球蛋白治疗系统性血管炎

ANCA anti-idiotype antibodies and the treatment of systemic vasculitis with intravenous immunoglobulin.

作者信息

Jayne D R, Esnault V L, Lockwood C M

机构信息

Department of Medicine, School of Clinical Medicine, University of Cambridge, UK.

出版信息

J Autoimmun. 1993 Apr;6(2):207-19. doi: 10.1006/jaut.1993.1018.

Abstract

The presence of anti-idiotype antibodies (anti-id) to anti-neutrophil cytoplasm autoantibodies (ANCA) in intravenous immunoglobulin (IVIg) and remission sera from patients with systemic vasculitis, and the use of IVIg as an alternative therapeutic agent in open studies, has suggested a role for idiotypic regulation in the normal control of these disorders. Clinical benefit with IVIg has been reported in 15/16 patients, with sustained remission in eight. The ability of IVIg to produce lasting remission has been associated with a fall in ANCA levels and stimulation of endogenous immunoglobulin production. IVIg has the potential to influence the pathogenetic process in patients with vasculitis at several stages, and an influence on the idiotypic regulation of ANCA may explain the observed clinical responses and point to possible targets for more specific immunotherapy in the future.

摘要

静脉注射免疫球蛋白(IVIg)以及系统性血管炎患者缓解期血清中存在针对抗中性粒细胞胞浆自身抗体(ANCA)的抗独特型抗体(抗-Id),并且在开放性研究中使用IVIg作为替代治疗药物,这表明独特型调节在这些疾病的正常控制中发挥作用。据报道,16例患者中有15例使用IVIg后临床获益,其中8例持续缓解。IVIg产生持久缓解的能力与ANCA水平下降及内源性免疫球蛋白产生受刺激有关。IVIg有可能在多个阶段影响血管炎患者的发病过程,对ANCA独特型调节的影响可能解释了观察到的临床反应,并为未来更特异性免疫治疗指出了可能的靶点。

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