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原发性免疫缺陷病患者的抗心磷脂抗体

Anticardiolipin antibodies in patients with primary immunodeficiency diseases.

作者信息

Pascual-Salcedo D, García Rodríguez M C, López Trascasa M, Fontán G

机构信息

Department of Laboratory Medicine, Hospital la Paz, Madrid, Spain.

出版信息

Ann Rheum Dis. 1988 May;47(5):410-3. doi: 10.1136/ard.47.5.410.

Abstract

The presence of antibodies to cardiolipin was determined (by an ELISA) in 143 patients with primary immunodeficiency diseases. Thirty (21%) had raised anticardiolipin antibody levels compared with only three in 98 age matched controls. The highest prevalence of this autoantibody was found in the Wiskott-Aldrich syndrome. Patients with selective IgA deficiency also showed a high prevalence of this autoantibody (32%), while patients with severe defects in antibody production showed a low prevalence or did not have such autoantibodies. This study provides further evidence of the association between autoimmune phenomena and primary immunodeficiency diseases.

摘要

通过酶联免疫吸附测定法(ELISA)检测了143例原发性免疫缺陷疾病患者体内抗心磷脂抗体的存在情况。与98名年龄匹配的对照组中仅3人相比,30例(21%)患者的抗心磷脂抗体水平升高。这种自身抗体在威斯科特-奥尔德里奇综合征中的患病率最高。选择性IgA缺乏症患者也显示出这种自身抗体的高患病率(32%),而抗体产生严重缺陷的患者患病率较低或不存在此类自身抗体。这项研究为自身免疫现象与原发性免疫缺陷疾病之间的关联提供了进一步的证据。

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