Olds G R, Kresina T F
International Health Institute, Department of Medicine, Miriam Hospital, Providence, RI 02906.
Parasite Immunol. 1990 Mar;12(2):199-211. doi: 10.1111/j.1365-3024.1990.tb00948.x.
A family of monoclonal antibodies (MoAb) was derived from the somatic cell fusion of P3NS1 myeloma cells and lymphoid cells from naturally infected mice of hyperimmunized mice. C57BL/6 mice were naturally infected with Schistosoma japonicum, and BALB/c mice were hyperimmunized with preparations of S. japonicum soluble egg antigens (SEA). The MoAbs which reflected the immune repertoire of naturally infected animals versus hyperimmune animals were characterized with regard to antibody isotype, antigen binding specificity, in-vitro immunosuppression of antigen-induced cell-mediated immune responses and the expression of SJ-CRIM, a major cross-reactive idiotype which appears on polyclonal anti-SEA antibodies generated during murine S. japonicum infection. The data indicate that for MoAbs of the IgG isotype which bound SEA by ELISA, the most immunosuppressive anti-SEA MoAbs identified expressed SJ-CRIM and were derived from naturally infected mice. All anti-SEA MoAbs expressing SJ-CRIM showed an identical banding pattern on immunoblot analysis which was abrogated by weak periodate treatment. The generation of expression of SJ-CRIM on MoAbs using differing methodologies across an allotype barrier indicates that the expression of SJ-CRIM is encoded by a germline gene. These data indicate an association between expression of this germline interstrain cross-reactive idiotype and immunosuppressive capacity. In addition, the immunoregulatory network which develops during immune S. japonicum infection is initiated by a carbohydrate epitope(s) found on various SEA. These data have profound implications in the use of the cross-reactive idiotype as a serodiagnostic tool in schistosomiasis.
一组单克隆抗体(MoAb)源自P3NS1骨髓瘤细胞与来自自然感染日本血吸虫的小鼠或经超免疫的小鼠的淋巴细胞的体细胞融合。C57BL/6小鼠自然感染日本血吸虫,BALB/c小鼠用日本血吸虫可溶性虫卵抗原(SEA)制剂进行超免疫。对反映自然感染动物与超免疫动物免疫库的单克隆抗体,在抗体亚型、抗原结合特异性、抗原诱导的细胞介导免疫反应的体外免疫抑制以及SJ-CRIM(一种主要的交叉反应独特型,出现在小鼠日本血吸虫感染期间产生的多克隆抗SEA抗体上)的表达方面进行了表征。数据表明,对于通过ELISA结合SEA的IgG亚型单克隆抗体,鉴定出的最具免疫抑制作用的抗SEA单克隆抗体表达SJ-CRIM,且源自自然感染的小鼠。所有表达SJ-CRIM的抗SEA单克隆抗体在免疫印迹分析中显示出相同的条带模式,该模式经弱高碘酸盐处理后消失。使用不同方法在同种异型屏障上产生的单克隆抗体上SJ-CRIM的表达表明,SJ-CRIM的表达由种系基因编码。这些数据表明这种种系间交叉反应独特型的表达与免疫抑制能力之间存在关联。此外,在日本血吸虫免疫感染期间形成的免疫调节网络是由各种SEA上发现的碳水化合物表位启动的。这些数据对交叉反应独特型作为血吸虫病血清诊断工具的应用具有深远意义。