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自身免疫性疾病患者中抗β2糖蛋白1抗体的IgG2亚类限制

IgG2 subclass restriction of anti-beta 2 glycoprotein 1 antibodies in autoimmune patients.

作者信息

Arvieux J, Roussel B, Ponard D, Colomb M G

机构信息

Laboratoires d'Immunologie Centre de Transfusion, Sanguine, France.

出版信息

Clin Exp Immunol. 1994 Feb;95(2):310-5. doi: 10.1111/j.1365-2249.1994.tb06529.x.

DOI:10.1111/j.1365-2249.1994.tb06529.x
PMID:8306507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1534919/
Abstract

The IgG subclass and light chain distribution of antiphospholipid antibodies (aPL) occurring in autoimmune patients were determined by means of two radioimmunoassays using either cardiolipin- or beta 2 glycoprotein 1 (beta 2GP1)-coated microtitre plates and mouse MoAbs. Of 50 sera selected for positivity of anticardiolipin antibodies (ACA) of the IgG isotype, 32 (64%) possessed anti-beta 2GP1 antibodies and their presence was closely associated with clinical features of the antiphospholipid syndrome. Good correlations were found between ACA and anti-beta 2GP1 antibodies when considering antibody level and patterns of light chain and IgG subclass, suggesting that, overall, the same antibodies were being measured. Light chain analysis showed the polyclonal origin of these antibodies and, in most sera, a trend towards use of lambda chain. Among sera positive for anti-beta 2GP1 antibodies, IgG2 was the major subclass reactive with beta 2GP1 and cardiolipin (87% and 74% of the IgG antibody activity, respectively). In contrast, in the group of 18 sera lacking anti-beta 2GP1 antibodies, ACA were largely restricted to IgG3, with a lesser contribution by IgG1. A few selected sera from the anti-beta 2GP1-positive group were shown to contain mixtures of antibodies that required beta 2GP1 (restricted to IgG2 present in large amounts) and did not require this cofactor (restricted to IgG3 and/or IgG1 present in low amounts) for their reactivity with cardiolipin. There was no contribution of glycosylation to the epitopes recognized by anti-beta 2GP1 antibodies, even though human anti-carbohydrate antibodies are restricted to the IgG2 subclass. These findings further emphasize the intra- and interindividual heterogeneity of aPL, and should help to discriminate clinically relevant specificies.

摘要

采用两种放射免疫分析法,分别使用包被心磷脂或β2糖蛋白1(β2GP1)的微量滴定板和小鼠单克隆抗体,测定自身免疫性疾病患者体内抗磷脂抗体(aPL)的IgG亚类和轻链分布。在50份IgG同种型抗心磷脂抗体(ACA)呈阳性的血清中,32份(64%)含有抗β2GP1抗体,其存在与抗磷脂综合征的临床特征密切相关。在考虑抗体水平、轻链模式和IgG亚类时,ACA与抗β2GP1抗体之间存在良好的相关性,这表明总体上检测的是相同的抗体。轻链分析显示这些抗体具有多克隆起源,并且在大多数血清中,存在使用λ链的趋势。在抗β2GP1抗体呈阳性的血清中,IgG2是与β2GP1和心磷脂反应的主要亚类(分别占IgG抗体活性的87%和74%)。相比之下,在18份缺乏抗β2GP1抗体的血清组中,ACA主要局限于IgG3,IgG1的贡献较小。从抗β2GP1阳性组中选取的一些血清显示含有抗体混合物,这些抗体与心磷脂反应时,有的需要β2GP1(大量存在的IgG2),有的不需要该辅因子(少量存在的IgG3和/或IgG1)。糖基化对抗β2GP1抗体识别的表位没有贡献,尽管人类抗碳水化合物抗体局限于IgG2亚类。这些发现进一步强调了aPL在个体内和个体间的异质性,并且有助于区分临床相关的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6362/1534919/45070eebf2fe/clinexpimmunol00022-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6362/1534919/45070eebf2fe/clinexpimmunol00022-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6362/1534919/45070eebf2fe/clinexpimmunol00022-0115-a.jpg

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