选择性IgA缺乏症患者自身免疫性疾病与抗IgA抗体的关联。

The association of autoimmune diseases and anti-IgA antibodies in patients with selective IgA deficiency.

作者信息

Petty R E, Palmer N R, Cassidy J T, Tubergen D G, Sullivan D B

出版信息

Clin Exp Immunol. 1979 Jul;37(1):83-8.

DOI:
PMID:314873
Abstract

The prevalence of antibodies to immunoglobulin A (IgA) was studied in eighty-three subjects with selective IgA deficiency (SIgAD), thirty-three normal individuals, thirty-two children with juvenile rheumatoid arthritis (JRA) and normal or elevated IgA, seventeen children with systemic lupus erythematosus (SLE) and normal or elevated IgA, and thirteen patients with hypogammaglobulinaemia. Anti-IgA antibodies were detected by haemagglutination of human erythrocytes coated with one of two IgA myelomas by the chromic chloride technique. Antibodies to IgA were not found in significant titre in individuals with normal or elevated IgA or in those with hypogammaglobulinaemia. In IgA deficient patients, elevated titres were found in 25--30% of those who were healthy or who had non-rheumatic diseases, 50% of those with rheumatoid arthritis, 77% of those with JRA and 100% of those with SLE. Patients with rheumatic diseases and SIgAD may therefore be particularly at risk of developing anti-IgA-mediated reactions to blood products.

摘要

对83例选择性免疫球蛋白A缺乏症(SIgAD)患者、33例正常个体、32例患有幼年类风湿性关节炎(JRA)且免疫球蛋白A正常或升高的儿童、17例患有系统性红斑狼疮(SLE)且免疫球蛋白A正常或升高的儿童以及13例低丙种球蛋白血症患者,研究了免疫球蛋白A(IgA)抗体的流行情况。采用氯化铬技术,通过用两种IgA骨髓瘤之一包被的人红细胞的血凝反应检测抗IgA抗体。在免疫球蛋白A正常或升高的个体或低丙种球蛋白血症患者中,未发现有显著滴度的抗IgA抗体。在IgA缺乏的患者中,25% - 30%健康或患有非风湿性疾病的患者、50%类风湿性关节炎患者、77% JRA患者以及100% SLE患者的抗体滴度升高。因此,患有风湿性疾病和SIgAD的患者可能特别有发生抗IgA介导的血液制品反应的风险。

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