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通过人单核细胞的分泌型免疫球蛋白A(sIgA)受体激活人单核细胞。

Activation of human monocytes via their sIgA receptors.

作者信息

Padeh S, Jaffe C L, Passwell J H

机构信息

Samuel Jared Kushnick Pediatric Immunology Laboratory, Sheba Medical Center, Sackler School of Medicine, Rehovot, Israel.

出版信息

Immunology. 1991 Feb;72(2):188-93.

PMID:2016119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1384482/
Abstract

We have studied the interaction of secretory immunoglobulin A (sIgA) derived from human breast milk with human monocytes. The presence of specific sIgA receptors on the monocyte membrane was confirmed by dose-dependent inhibition of E-sIgA rosette formation and by the binding of iodinated sIgA to monocyte monolayers. Binding was dependent on both the number of monocytes, as well as the amount of [125I]sIgA, and could be inhibited by unlabelled sIgA. Incubation of monocyte monolayers in the presence of increasing concentrations of secretory IgA and F(ab')2 anti-IgA resulted in a dose-dependent increase of the oxidative burst, as measured by H2O2 production. Neither sIgA or anti-IgA alone, nor incubation of IgG with anti-IgA, had any effect on the oxidative burst. These studies indicate that human monocytes have a receptor for sIgA and that specific activation of the monocytes occurs via these receptors.

摘要

我们研究了源自人母乳的分泌型免疫球蛋白A(sIgA)与人单核细胞的相互作用。通过剂量依赖性抑制E-sIgA玫瑰花结形成以及碘化sIgA与单核细胞单层的结合,证实了单核细胞膜上存在特异性sIgA受体。结合既取决于单核细胞的数量,也取决于[125I]sIgA的量,并且可被未标记的sIgA抑制。在存在浓度不断增加的分泌型IgA和F(ab')2抗IgA的情况下孵育单核细胞单层,通过H2O2产生量测定,导致氧化爆发呈剂量依赖性增加。单独的sIgA或抗IgA,以及IgG与抗IgA一起孵育,对氧化爆发均无任何影响。这些研究表明,人单核细胞具有sIgA受体,并且单核细胞通过这些受体发生特异性激活。

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本文引用的文献

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Abrogation of macrophage-dependent injury in experimental glomerulonephritis in the rabbit. Use of an antimacrophage serum.兔实验性肾小球肾炎中巨噬细胞依赖性损伤的消除。抗巨噬细胞血清的应用。
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Subpopulations of human peripheral granulocyes and monocytes express receptors for IgA.人类外周粒细胞和单核细胞的亚群表达IgA受体。
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Dynamics of mononuclear phagocyte system Fc receptor function in systemic lupus erythematosus. Relation to disease activity and circulating immune complexes.系统性红斑狼疮中单核吞噬细胞系统Fc受体功能的动力学。与疾病活动和循环免疫复合物的关系。
Clin Exp Immunol. 1983 Feb;51(2):261-8.
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