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自身免疫性风湿疾病中常见独特型PR4的研究。

Studies of a common idiotype PR4 in autoimmune rheumatic disease.

作者信息

Williams W, Zumla A, Behrens R, Locniskar M, Voller A, McAdam K P, Isenberg D A

机构信息

Bloomsbury Rheumatology Unit/Department of Rheumatology Research, University College, London, United Kingdom.

出版信息

Arthritis Rheum. 1988 Sep;31(9):1097-104. doi: 10.1002/art.1780310903.

Abstract

A new common idiotype, designated PR4, is described. This idiotype was originally identified on a human hybridoma-derived monoclonal antibody from a patient with leprosy, which binds the major Mycobacterium leprae-derived antigen, phenolic glycolipid-1, poly(ADP)-ribose, DNA, and poly(dT). The PR4 idiotype was found in patients with systemic lupus erythematosus (SLE) (70%), rheumatoid arthritis (40%), and Sjögren's syndrome (15%). It was not, however, found in the spouses of the SLE patients or (unlike other lupus idiotypes) in their healthy first-degree relatives. Although no correlation between PR4 idiotype levels and disease activity in SLE was found, a subset of rheumatoid arthritis patients with high levels of the idiotype was identified.

摘要

描述了一种新的共同独特型,命名为PR4。这种独特型最初是在一名麻风病患者的人杂交瘤衍生单克隆抗体上鉴定出来的,该抗体可结合麻风分枝杆菌的主要抗原、酚糖脂-1、聚(ADP)-核糖、DNA和聚(dT)。在系统性红斑狼疮(SLE)患者(70%)、类风湿性关节炎患者(40%)和干燥综合征患者(15%)中发现了PR4独特型。然而,在SLE患者的配偶中未发现该独特型,(与其他狼疮独特型不同)在其健康的一级亲属中也未发现。虽然未发现PR4独特型水平与SLE疾病活动之间存在相关性,但已鉴定出一部分该独特型水平较高的类风湿性关节炎患者。

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