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独特型操作诱导的系统性红斑狼疮和抗磷脂综合征实验模型的意义

The significance of experimental models of systemic lupus erythematosus and antiphospholipid syndrome induced by idiotypic manipulation.

作者信息

Shoenfeld Y

机构信息

Department of Medicine B, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

出版信息

Isr J Med Sci. 1994 Jan;30(1):10-8.

PMID:8138385
Abstract

Systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APLS) are two related autoimmune conditions. The pathogenesis of the diseases is unclear and the etiology is multifactorial. During the last 8 years our laboratory has been involved in induction of experimental SLE and APLS both by passive transfer of pathogenic antibodies (e.g., anticardiolipin) and by active immunization with pathogenic idiotypes. The naive mice, following immunization with Ab1, develop anti-autoantibody (Ab2) and eventually anti-autoantibody (Ab3) which has the binding capacities of anti-DNA or anticardiolipin. The mice with the characteristic syndromes were employed to analyze pathogenic mechanisms and new therapeutic modalities.

摘要

系统性红斑狼疮(SLE)和抗磷脂综合征(APLS)是两种相关的自身免疫性疾病。这些疾病的发病机制尚不清楚,病因是多因素的。在过去8年中,我们的实验室一直致力于通过致病性抗体(如抗心磷脂抗体)的被动转移和致病性独特型的主动免疫来诱导实验性SLE和APLS。未免疫的小鼠在接种Ab1后,会产生抗自身抗体(Ab2),最终产生具有抗DNA或抗心磷脂结合能力的抗自身抗体(Ab3)。具有特征性综合征的小鼠被用于分析致病机制和新的治疗方法。

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