Grzych J M, Capron M, Dissous C, Capron A
J Immunol. 1984 Aug;133(2):998-1004.
Rat IgG2c monoclonal antibodies have been produced after fusion of spleen cells from LOU/C rats infected with Schistosoma mansoni for 5 wk and IRF983F nonsecreting rat myeloma. The cell supernatant of an IgG2c-producing clone (IPLSm3), as well as ascitic fluids induced by this clone, revealed anti-S. mansoni activity detected by immunofluorescence on schistosomula sections. Antigenic analysis performed with IPLSm3 IgG2c antibody allowed to isolate onto the S. mansoni schistosomula surface a 38,000 dalton antigen previously characterized with the protective IPLSm1 IgG2a monoclonal antibody. Although IPLSm3 IgG2c did not exhibit any killing activity in vitro against schistosomula in the presence of complement, macrophages, or eosinophils, it was shown to strongly inhibit the eosinophil-dependent cytotoxicity mediated by IPLSm1 IgG2a antibodies. The blocking activity of IgG2c antibody was further demonstrated in vitro by the use of F(ab')2 fragments and in vivo by the inhibition of passively transferred immunity conferred by the IgG2a protective monoclonal antibody. These results indicate that blocking antibodies could play an important role in the expression of protective immunity during schistosome infection.
将感染曼氏血吸虫5周的LOU/C大鼠的脾细胞与IRF983F非分泌型大鼠骨髓瘤细胞融合后,制备出了大鼠IgG2c单克隆抗体。产生IgG2c的克隆(IPLSm3)的细胞上清液以及由该克隆诱导产生的腹水,在血吸虫童虫切片上通过免疫荧光检测显示出抗曼氏血吸虫活性。用IPLSm3 IgG2c抗体进行的抗原分析,使得能够在曼氏血吸虫童虫表面分离出一种38,000道尔顿的抗原,该抗原先前已用具有保护性的IPLSm1 IgG2a单克隆抗体进行了鉴定。尽管在有补体、巨噬细胞或嗜酸性粒细胞存在的情况下,IPLSm3 IgG2c在体外对血吸虫童虫没有表现出任何杀伤活性,但它被证明能强烈抑制由IPLSm1 IgG2a抗体介导的嗜酸性粒细胞依赖性细胞毒性。通过使用F(ab')2片段在体外进一步证明了IgG2c抗体的阻断活性,并通过抑制IgG2a保护性单克隆抗体赋予的被动转移免疫在体内证明了其阻断活性。这些结果表明,阻断抗体可能在血吸虫感染期间保护性免疫的表达中发挥重要作用。