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类风湿关节炎中性粒细胞减少病例及自身免疫性中性粒细胞减少症中缺乏粒细胞特异性膜导向自身抗体的证据。

Lack of evidence for granulocyte specific membrane-directed autoantibodies in neutropenic cases of rheumatoid arthritis and in autoimmune neutropenia.

作者信息

Petersen J, Wiik A

出版信息

Acta Pathol Microbiol Immunol Scand C. 1983 Feb;91(1):15-22.

PMID:6346799
Abstract

With the purpose of detecting granulocyte-specific membrane-directed autoantibodies, IgG was isolated from 14 patients with Felty's syndrome, from 5 patients with rheumatoid arthritis associated with neutropenia, and from 3 rheumatoid factor positive patients with autoimmune neutropenia. By means of indirect immunofluorescence suspensions of leukocytes from healthy controls were tested for their ability to bind whole IgG fractions or F(ab')2 fragments of IgG isolated from the neutropenic patients. By this method, whole IgG preparations from neutropenic patients and normal controls were invariably found to bind to the surface of granulocytes and a minor proportion of lymphocytes. In contrast. F(ab')2 fragments of IgG from the neutropenic patients failed to bind to the surface of granulocytes. Both whole IgG fractions and F(ab')2 fragments displayed displayed antinuclear antibody activity ruling out the possibility of loss of antibody reactivity during the preparation of F(ab')2 fragments. The neutropenia seen in rheumatoid arthritis with or without splenomegaly thus does not seem to be induced by granulocyte-specific membrane-directed IgG autoantibodies, but rather by a non-specific attachment of IgG most probably in immune complex bound form to Fc gamma receptors on neutrophils which thereby acquire surface properties facilitating removal from the circulating blood cell pool.

摘要

为了检测粒细胞特异性膜导向自身抗体,从14例费尔蒂综合征患者、5例伴有中性粒细胞减少的类风湿关节炎患者以及3例类风湿因子阳性的自身免疫性中性粒细胞减少患者中分离出IgG。通过间接免疫荧光法,检测来自健康对照者的白细胞悬液与从中性粒细胞减少患者分离出的完整IgG组分或IgG的F(ab')2片段结合的能力。通过这种方法,始终发现中性粒细胞减少患者和正常对照者的完整IgG制剂可与粒细胞表面以及一小部分淋巴细胞结合。相比之下,中性粒细胞减少患者的IgG的F(ab')2片段未能与粒细胞表面结合。完整IgG组分和F(ab')2片段均显示出抗核抗体活性,排除了在制备F(ab')2片段过程中抗体反应性丧失的可能性。因此,无论有无脾肿大,类风湿关节炎中出现的中性粒细胞减少似乎并非由粒细胞特异性膜导向IgG自身抗体诱导,而是由IgG以免疫复合物结合形式非特异性地附着于中性粒细胞上的Fcγ受体所致,中性粒细胞由此获得便于从循环血细胞池中清除的表面特性。

相似文献

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Lack of evidence for granulocyte specific membrane-directed autoantibodies in neutropenic cases of rheumatoid arthritis and in autoimmune neutropenia.类风湿关节炎中性粒细胞减少病例及自身免疫性中性粒细胞减少症中缺乏粒细胞特异性膜导向自身抗体的证据。
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引用本文的文献

1
Immune complexes and the pathogenesis of neutropenia in Felty's syndrome.免疫复合物与费尔蒂综合征中性粒细胞减少症的发病机制
Ann Rheum Dis. 1986 Aug;45(8):696-702. doi: 10.1136/ard.45.8.696.