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人类抗IgG自身抗体(类风湿因子)上交叉反应独特型的分子基础。

Molecular basis for the cross-reactive idiotypes on human anti-IgG autoantibodies (rheumatoid factors).

作者信息

Carson D A, Chen P P, Kipps T J, Radoux V, Jirik F, Goldfien R D, Fox R I, Silverman G J, Fong S

机构信息

Department of Basic and Clinical Research, Scripps Clinic and Research Foundation, La Jolla, California 92037.

出版信息

Ciba Found Symp. 1987;129:123-34. doi: 10.1002/9780470513484.ch9.

Abstract

High titres of anti-IgG autoantibodies (rheumatoid factors, RF) are characteristic of patients with rheumatoid arthritis, Sjögren's syndrome, and mixed cryoglobulinaemia, and may contribute to immune complex formation and tissue damage. The monoclonal RFs from cryoglobulinaemia patients frequently display cross-reactive idiotypes. The genetic basis for the cross-reactive idiotypes on RF autoantibodies has not been determined. To clarify structural and genetic relationships among RFs from unrelated subjects, a series of anti-peptide antibodies have been generated that define primary sequence-dependent idiotypes on RF heavy and light chains. Multiple monoclonal and polyclonal RFs from unrelated individuals have been probed by Western blotting with the anti-idiotypic reagents. The results show that sequences in the kappa light chain variable region represent a common structural element among RF autoantibodies. This hypothesis is confirmed by the cloning and sequencing of the conserved germline variable region gene which encodes human RF kappa chains.

摘要

高滴度的抗IgG自身抗体(类风湿因子,RF)是类风湿性关节炎、干燥综合征和混合性冷球蛋白血症患者的特征,可能有助于免疫复合物的形成和组织损伤。冷球蛋白血症患者的单克隆RF经常显示交叉反应独特型。RF自身抗体上交叉反应独特型的遗传基础尚未确定。为了阐明来自无关个体的RF之间的结构和遗传关系,已经产生了一系列抗肽抗体,这些抗体定义了RF重链和轻链上依赖于一级序列的独特型。用抗独特型试剂通过蛋白质印迹法检测了来自无关个体的多种单克隆和多克隆RF。结果表明,κ轻链可变区的序列代表了RF自身抗体中的一个共同结构元件。通过对编码人RF κ链的保守种系可变区基因的克隆和测序,证实了这一假设。

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