Pan A A, McMahon-Pratt D
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06510-8034.
J Immunol. 1989 Aug 1;143(3):1001-8.
Stage-specific mAb have been produced to amastigotes and epimastigotes of Trypanosoma cruzi (Brazil strain). mAb C-1 through C-6 reacted specifically with T. cruzi strains; no cross-reactions were found with membranes of promastigotes or amastigotes of Leishmania species. One mAb produced against the epimastigote membranes (C-5) was found to be specific against this stage by radioimmune binding assay, immunofluorescence, and radioimmunoprecipitation. mAb C-5 recognized a novel epimastigote protein at Mr (greater than 200,000) on immunoprecipitation with radiolabeled epimastigotes. Three amastigote stage-specific monoclonal antibodies were produced against membrane-enriched preparations of T. cruzi (Brazil strain) amastigotes grown in axenic culture (C-1 through C-3). By indirect immunofluorescence assay, monoclonal antibody C-2 bound only to T. cruzi amastigotes; no reaction with either tissue culture-derived trypomastigotes or epimastigotes was observed. mAb C-1 and C-2 each specifically immunoprecipitated a single protein molecule with Mr 83,000 from [35S]-methionine-labeled amastigotes. mAb C-2 was also used to affinity purify an 83-kDa Ag that was recognized by human Chagasic sera from patients of endemic countries of Latin America in an enzyme immunoassay. Amino acid composition and preliminary sequence data of the 83-kDa protein are presented. These mAb and/or purified Ag may be useful in studying stage differentiation, monitoring transformation, and for further taxonomic, epidemiologic, and immunologic studies of Chagas' disease.
已经制备了针对克氏锥虫(巴西株)无鞭毛体和上鞭毛体的阶段特异性单克隆抗体。单克隆抗体C-1至C-6与克氏锥虫菌株特异性反应;未发现与利什曼原虫属前鞭毛体或无鞭毛体膜有交叉反应。通过放射免疫结合试验、免疫荧光和放射免疫沉淀法发现,一种针对上鞭毛体膜产生的单克隆抗体(C-5)对该阶段具有特异性。单克隆抗体C-5在用放射性标记的上鞭毛体进行免疫沉淀时,识别出一种分子量大于200,000的新型上鞭毛体蛋白。针对在无细胞培养中生长的克氏锥虫(巴西株)无鞭毛体的富含膜的制剂,制备了三种无鞭毛体阶段特异性单克隆抗体(C-1至C-3)。通过间接免疫荧光试验,单克隆抗体C-2仅与克氏锥虫无鞭毛体结合;未观察到与组织培养衍生的锥鞭毛体或上鞭毛体有反应。单克隆抗体C-1和C-2各自从[35S]-甲硫氨酸标记的无鞭毛体中特异性免疫沉淀出一种分子量为83,000的单一蛋白质分子。单克隆抗体C-2还用于亲和纯化一种83-kDa抗原,在酶免疫测定中,该抗原可被来自拉丁美洲流行国家患者的人类恰加斯病血清识别。本文给出了83-kDa蛋白的氨基酸组成和初步序列数据。这些单克隆抗体和/或纯化的抗原可能有助于研究阶段分化、监测转化,以及用于恰加斯病的进一步分类学、流行病学和免疫学研究。