Horowitz S, Tarrab-Hazdai R, Eshhar Z, Arnon R
Apartment of Chemical Immunology, The Weizmann Institute of Science, Rehovot, Israel.
EMBO J. 1983;2(2):193-8. doi: 10.1002/j.1460-2075.1983.tb01404.x.
Five monoclonal antibodies specific towards Schistosoma mansoni antigens were prepared by fusion of spleen cells of infected and immunized mouse with the murine myeloma NS-1 cells. Three of the five antibodies belonged to the IgG1 class, one was an IgM and the fifth one was an IgE. The IgE monoclonal antibody designated 54.10, induced antigen-specific degranulation of rat basophilic cell line, a property which served as the basis for the screening assay. Its biological function was demonstrated by a specific macrophage activation that led to killing of schistosomula; no such killing was obtained with anti-schistosome antibodies of other classes or with IgE of different antigenic specificity. The second monoclonal antibody of biological significance was an IgG1, designated 27.21 which is reactive in the immunofluorescence staining of surface antigens on intact schistosomula. All three monoclonal antibodies that belonged to the IgG1 class were effective in mediating killing of schistosomula by complement, with the highest effect exerted by 27.21. It is thus apparent that the 27.21 monoclonal antibody is directed against a densely distributed surface antigen on the schistosomula membrane which is possibly involved in the protective immunity. Preliminary data showed that immunoprecipitation with the 27.21 antibodies results in the isolation of three major protein bands, of 60 kd, 50 kd, 19 kd, respectively.
通过将感染并免疫的小鼠脾细胞与鼠骨髓瘤NS-1细胞融合,制备了五种针对曼氏血吸虫抗原的单克隆抗体。这五种抗体中,三种属于IgG1类,一种是IgM,第五种是IgE。名为54.10的IgE单克隆抗体可诱导大鼠嗜碱性细胞系发生抗原特异性脱颗粒,这一特性是筛选试验的基础。其生物学功能通过特异性巨噬细胞激活得以证明,该激活导致血吸虫童虫被杀伤;而其他类别的抗血吸虫抗体或具有不同抗原特异性的IgE则无法产生这种杀伤作用。具有生物学意义的第二种单克隆抗体是一种IgG1,名为27.21,它在完整血吸虫童虫表面抗原的免疫荧光染色中具有反应性。所有三种属于IgG1类的单克隆抗体在介导补体杀伤血吸虫童虫方面均有效,其中27.21的效果最佳。因此很明显,27.21单克隆抗体针对的是血吸虫童虫膜上密集分布的一种表面抗原,该抗原可能参与保护性免疫。初步数据显示,用27.21抗体进行免疫沉淀可分别分离出三条主要蛋白带,分子量分别为60 kd、50 kd、19 kd。