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大鼠免疫球蛋白及免疫复合物的趋化特性。

Chemotactic properties of rat immunoglobulins and immune complexes.

作者信息

Arashi M, Sibille Y, Merrill W W, Rits M, Bazin H, Vaerman J P

机构信息

Unit of Experimental Medicine, Catholic University of Louvain, Belgium.

出版信息

Infect Immun. 1989 Feb;57(2):452-7. doi: 10.1128/iai.57.2.452-457.1989.

Abstract

The effect of rat immunoglobulins and immune complexes on the locomotor function of rat polymorphonuclear leukocytes (PMN) was investigated in vitro. Rat immunoglobulin G1 (IgG1), IgG2a, IgG2b, and IgA monoclonal antibodies specific for the dinitrophenyl hapten were used. Both monomeric and polymeric IgA showed chemotactic activity in a dose-dependent manner. IgG1 and IgG2b also induced a dose-dependent locomotor response of PMN, but the nature of the induced migration was chemokinetic (enhancing random migration). IgG2a was chemotactic and induced maximal migration at a relatively low concentration. IgG1- and IgG2b-immune complexes induced stronger migration than antibody alone; however, IgA- and IgG2a-immune complexes did not. IgA was shown to modify the chemotactic movement of PMN induced by N-formylmethionyl-leucyl-phenylalanine (FMLP). In the presence of both IgA and FMLP in the lower chamber, the migration towards suboptimal concentrations of FMLP was enhanced. By contrast, IgA in the upper chamber decreased migration towards the optimal or higher concentrations of FMLP. These findings suggest that IgA may work synergistically with luminal chemoattractants to mobilize PMN to the locus of infection on the mucosal surface. In addition, the intense activity of IgG2a alone and IgG1- or IgG2b-immune complexes in inducing PMN migration may play an important role in inflammatory processes. The data indicate that immunoglobulins have a direct effect on PMN mobility.

摘要

在体外研究了大鼠免疫球蛋白和免疫复合物对大鼠多形核白细胞(PMN)运动功能的影响。使用了对二硝基苯基半抗原具有特异性的大鼠免疫球蛋白G1(IgG1)、IgG2a、IgG2b和IgA单克隆抗体。单体和多聚体IgA均呈剂量依赖性地表现出趋化活性。IgG1和IgG2b也诱导PMN产生剂量依赖性的运动反应,但诱导的迁移性质是化学动力学的(增强随机迁移)。IgG2a具有趋化性,并在相对较低浓度下诱导最大迁移。IgG1和IgG2b免疫复合物比单独抗体诱导更强的迁移;然而,IgA和IgG2a免疫复合物则不然。已证明IgA可改变由N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)诱导的PMN趋化运动。在下室同时存在IgA和FMLP的情况下,向次优浓度FMLP的迁移增强。相比之下,上室中的IgA会减少向最佳或更高浓度FMLP的迁移。这些发现表明,IgA可能与腔内趋化因子协同作用,将PMN动员到粘膜表面的感染部位。此外,单独的IgG2a以及IgG1或IgG2b免疫复合物在诱导PMN迁移方面的强烈活性可能在炎症过程中起重要作用。数据表明免疫球蛋白对PMN的迁移具有直接影响。

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