Kennedy M W, McIntosh A E, Blair A J, McLaughlin D
Wellcome Laboratories for Experimental Parasitology, University of Glasgow, Bearsden.
Immunology. 1990 Nov;71(3):317-22.
It might be expected that infections with transmissible agents will elicit an immune response to all of their exoantigens and that immune response (Ir) gene control of responses to individual epitopes on a given parasite component would be obscured by reaction to the molecule as a whole. Humans infected with parasitic nematodes, however, mount antibody responses which are selective for certain parasite components. This was modelled in inbred rats infected with the parasitic nematode Nippostrongylus brasiliensis and their responses to secreted antigens analysed by immunoprecipitation and SDS-PAGE. No strain responded to all the potential antigens and only those of identical major histocompatibility complex (MHC) had similar recognition profiles. This MHC-restricted response applied to whole molecules synthesized by the parasite, rather than merely to epitopes thereon and is, therefore, contrary to expectation. Moreover, the response patterns of F1 hybrid animals were not merely summations of parental responses. This suggests defective antigen presentation of particular parasite components by certain MHC class II molecules and/or cross-tolerance with background gene products.
人们可能会认为,感染可传播病原体后会引发针对其所有外抗原的免疫反应,而且对给定寄生虫成分上各个表位的免疫反应(Ir)基因控制会因对整个分子的反应而变得模糊不清。然而,感染寄生线虫的人类会产生针对某些寄生虫成分的选择性抗体反应。这在感染巴西日圆线虫的近交系大鼠中得到了模拟,并通过免疫沉淀和SDS - PAGE分析了它们对分泌抗原的反应。没有一个品系对所有潜在抗原都有反应,只有那些主要组织相容性复合体(MHC)相同的品系才有相似的识别模式。这种MHC限制的反应适用于寄生虫合成的整个分子,而不仅仅是其上的表位,因此与预期相反。此外,F1杂交动物的反应模式不仅仅是亲本反应的总和。这表明某些MHC II类分子对特定寄生虫成分的抗原呈递存在缺陷和/或与背景基因产物存在交叉耐受性。