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加蓬个体中罗阿丝虫抗原的IgG亚类识别及其与临床状态的相关性

IgG subclass recognition of Loa loa antigens and their correlation with clinical status in individuals from Gabon.

作者信息

Akue J P, Hommel M, Devaney E

机构信息

Centre International de Recherches Medicales de Franceville, BP 769, Franceville, Gabon.

出版信息

Parasite Immunol. 1998 Aug;20(8):387-93. doi: 10.1046/j.1365-3024.1998.00172.x.

Abstract

In endemic areas for Loa loa, a significant percentage of actively infected individuals have no circulating microfilariae, an observation which implies the existence of a stage-specific immune response. In an attempt to define the immunological basis of the amicrofilaraemic state, the reactivity of antigens from adult, microfilariae and infective larvae of L. loa was examined by Western blotting with individual serum samples from four clinically defined groups (high microfilaraemic, low microfilaraemic, amicrofilaraemic and endemic controls) using IgG subclass-specific reagents and IgE. In the adult parasite, a complex of antigens at 28-31 kDa was exclusively recognized by IgG1 from amicrofilaraemic individuals and, to a lesser extent, by IgG1 from endemic controls. However, this complex of antigens was recognized by IgG4 antibodies in serum samples from all individuals, including microfilaraemics. A microfilarial antigen of 21 kDa was recognized by IgG1 antibodies present in serum from amicrofilaraemic, endemic control and low microfilaraemic individuals. Persons with high levels of microfilariae did not recognise this antigen. In both the L3 and the microfilariae, a ladder antigen with increments of 15 kDa was the main target of IgG4 antibodies in amicrofilaraemic and microfilaraemic individuals. IgE antibodies recognized more antigens in the microfilarial stage than in the adult of L3. These results suggest that immunological differences between clinically defined groups are associated with the recognition of different antigens or epitopes.

摘要

在罗阿丝虫病的流行地区,相当大比例的活跃感染者体内没有循环微丝蚴,这一观察结果表明存在阶段特异性免疫反应。为了确定无微丝蚴血症状态的免疫基础,使用IgG亚类特异性试剂和IgE,通过蛋白质印迹法,用来自四个临床定义组(高微丝蚴血症组、低微丝蚴血症组、无微丝蚴血症组和流行地区对照组)的个体血清样本检测罗阿丝虫成虫、微丝蚴和感染性幼虫的抗原反应性。在成虫寄生虫中,28 - 31 kDa的抗原复合物仅被无微丝蚴血症个体的IgG1识别,在较小程度上也被流行地区对照组的IgG1识别。然而,所有个体(包括微丝蚴血症患者)血清样本中的IgG4抗体都能识别这种抗原复合物。21 kDa的微丝蚴抗原被无微丝蚴血症个体、流行地区对照组和低微丝蚴血症个体血清中的IgG1抗体识别。微丝蚴水平高的人不识别这种抗原。在L3和微丝蚴中,15 kDa递增的阶梯状抗原是无微丝蚴血症和微丝蚴血症个体中IgG4抗体的主要靶标。与L3成虫相比,IgE抗体在微丝蚴阶段识别的抗原更多。这些结果表明,临床定义组之间的免疫差异与不同抗原或表位的识别有关。

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