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神经系统疾病中的抗心磷脂抗体:与抗单链DNA活性的交叉反应

Anti-cardiolipin antibodies in neurological disorders: cross-reaction with anti-single stranded DNA activity.

作者信息

Colaço C B, Scadding G K, Lockhart S

机构信息

Department of Rheumatology, Middlesex Hospital Medical School, London, UK.

出版信息

Clin Exp Immunol. 1987 May;68(2):313-9.

Abstract

Antiphospholipid (PL) antibodies have been detected in sera from patients with chronic neurological diseases associated with disorders of immunity. In an isotype specific radioimmunoassay for anti-cardiolipin (CL) antibodies, we found IgM anti-CL (greater than 2 s.d. above mean of controls) in 17/25 (68%) patients with myasthenia gravis (MG), 8/25 (32%) with the Lambert-Eaton myasthenic syndrome (LEMS), 5/17 (29%) with multiple sclerosis and 3/11 (27%) cases of migraine. IgG anti-CL was only found in low titres in sera from 10 patients with MG and three with LEMS. Significant anti-CL activity could not be detected in sera from nine patients with acute Guillain-Barré Syndrome (GBS), 12 chronic cases of epilepsy, 8/9 with oat cell carcinoma and 9/10 with acute stroke. Further tests on 39 sera with the highest anti-CL activity, from all of the above disease groups, showed a significant correlation between IgM anti-CL and IgM anti-ss DNA activities. In a series of competitive inhibition assays six sera from patients with MG were shown to have a proportion of both specific and cross-reactive IgM anti-CL and IgM anti-ss DNA antibodies. Anti-phospholipid antibodies occur in certain neurological diseases, at lower titres than seen in SLE, yet their cross-reactive binding to ss DNA suggests similar antibacterial origins as have been proposed for lupus auto-antibodies. In the absence of overt infection they might reflect a breakdown of tolerance for non-organ specific membrane antigens in diseases with predominantly organ specific membrane bound putative autoimmunogens.

摘要

在患有与免疫紊乱相关的慢性神经疾病患者的血清中检测到了抗磷脂(PL)抗体。在一项针对抗心磷脂(CL)抗体的同型特异性放射免疫分析中,我们发现,在25例重症肌无力(MG)患者中有17例(68%)IgM抗CL(高于对照组均值2个标准差以上),25例兰伯特-伊顿肌无力综合征(LEMS)患者中有8例(32%),17例多发性硬化症患者中有5例(29%),11例偏头痛患者中有3例(27%)。仅在10例MG患者和3例LEMS患者的血清中发现低滴度的IgG抗CL。在9例急性格林-巴利综合征(GBS)患者、12例慢性癫痫患者、9例燕麦细胞癌患者中的8例以及10例急性中风患者中的9例的血清中未检测到显著的抗CL活性。对上述所有疾病组中抗CL活性最高的39份血清进行的进一步检测显示,IgM抗CL与IgM抗单链DNA活性之间存在显著相关性。在一系列竞争性抑制试验中,6例MG患者的血清显示同时具有一定比例的特异性和交叉反应性IgM抗CL及IgM抗单链DNA抗体。抗磷脂抗体存在于某些神经疾病中,其滴度低于系统性红斑狼疮(SLE)中的滴度,但其与单链DNA的交叉反应性结合表明其与狼疮自身抗体具有相似的抗菌起源。在没有明显感染的情况下,它们可能反映了在以器官特异性膜结合假定自身免疫原为主要特征的疾病中,对非器官特异性膜抗原的耐受性破坏。

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