Cramer M, Braun D G
J Exp Med. 1973 Dec 1;138(6):1533-44. doi: 10.1084/jem.138.6.1533.
Immunization of BALB/c mice with Group A streptococcal vaccines leads to the induction of high levels of monoclonal antibody populations. Subsequent immunization of these mice with Group A-variant streptococcal vaccines induces a significant level of monoclonal antibody of A-variant antigen specificity revealed by labeled group A-variant polysaccharide. During these course Av and Av' immunizations, the monoclonal Group A-specific antibodies were also restimulated to levels usually higher than the variant-specific antibodies. With two exceptions, these homogeneous antibody populations were not cross-reactive in vitro with the related antigen. Such cross-stimulation of monoclonal antibodies was interpreted as a function of particular membrane properties of the Ig receptor-bearing memory cells which, for restimulation, would only require the structurally closely related antigen which serves as a backbone to the original antigen, and not necessarily the exact fit of the homologous immunodominant group.
用A组链球菌疫苗免疫BALB/c小鼠可诱导产生高水平的单克隆抗体群体。随后用A组变异链球菌疫苗对这些小鼠进行免疫,可诱导出由标记的A组变异多糖所揭示的具有显著水平的A变异抗原特异性单克隆抗体。在这些Av和Av'免疫过程中,单克隆A组特异性抗体也被重新刺激到通常高于变异特异性抗体的水平。除了两个例外情况,这些同源抗体群体在体外与相关抗原无交叉反应。单克隆抗体的这种交叉刺激被解释为携带Ig受体的记忆细胞的特定膜特性的作用,对于重新刺激而言,这种记忆细胞仅需要作为原始抗原主干的结构密切相关的抗原,而不一定需要同源免疫显性基团的精确匹配。