Hashimoto N, Takatsu K, Masuho Y, Kishida K, Hara T, Hamaoka T
J Immunol. 1984 Jan;132(1):129-35.
A covalent conjugate of avidin with ricin subunit A-chain (avidin-RA) was prepared by using N-succinimidyl 3-(2-pyridyldithio)propionate as a coupling agent. Selective cytotoxic activity after the combined treatment of spleen cells with biotinylated antibody and avidin-RA was demonstrated by the fact that the responsiveness to LPS was selectively abrogated by pretreatment of the cells with biotinylated rabbit anti-mouse immunoglobulin (MIg) antibody, but not with biotinylated anti-Thy-1.2 antibody. Neither the biotinylated antibody alone nor avidin-RA alone was effective in decreasing the responses to mitogens. Moreover, a high anti-DNP PFC response elicited by DNP-KLH-primed BALB/c mouse spleen cells stimulated in vitro with DNP-KLH was mostly abrogated by the pretreatment of the cells with biotinylated anti-MIg antibody and avidin-RA. Again, neither the biotinylated antibody alone nor avidin-RA alone was effective in decreasing the anti-DNP PFC response. This cell-killing method with the use of biotinylated antibody and avidin-RA was applied and evaluated in experimental systems in which the helper action of T cells on B cells was mediated by T cell-replacing factor (TRF) or was performed by the direct interaction of T cells with B cells (cognate interaction). When DNP-KLH-primed splenic B cells, pretreated with biotinylated F(ab')2 fragment of DCF1 male anti-BALB/c-B IgG antibody against acceptor site(s) for TRF followed by treatment with avidin-RA, were stimulated with DNP-OVA in the presence of monoclonal TRF, the anti-DNP PFC response was significantly decreased, whereas the same treated B cells responded well to stimulation with DNP-PPD in the presence of Tbc-primed T cells (cognate interaction). These results indicate that B cells responsible for the cognate interaction and those having TRF acceptor site(s) belong to a distinct subpopulation of B cells, and that the cytocidal action of the noncovalent conjugate of the antibody and RA formed from the biotinylated antibody and avidin-RA via an avidin-biotin complex has immunologic selectivity, eliminating only the latter subset of B cells recognized by the antibody.
以N - 琥珀酰亚胺基3 -(2 - 吡啶二硫基)丙酸酯作为偶联剂制备了抗生物素蛋白与蓖麻毒素A链的共价偶联物(抗生物素蛋白 - RA)。用生物素化抗体和抗生物素蛋白 - RA联合处理脾细胞后,显示出选择性细胞毒性活性,这一事实表明,用生物素化兔抗小鼠免疫球蛋白(MIg)抗体预处理细胞可选择性消除对脂多糖的反应性,但用生物素化抗Thy - 1.2抗体预处理则无此效果。单独的生物素化抗体或单独的抗生物素蛋白 - RA均不能有效降低对有丝分裂原的反应。此外,用生物素化抗MIg抗体和抗生物素蛋白 - RA预处理DNP - KLH致敏的BALB / c小鼠脾细胞,这些细胞在体外被DNP - KLH刺激后引发的高抗DNP PFC反应大多被消除。同样,单独使用生物素化抗体或单独使用抗生物素蛋白 - RA均不能有效降低抗DNP PFC反应。这种使用生物素化抗体和抗生物素蛋白 - RA的细胞杀伤方法在实验系统中得到应用和评估,在这些实验系统中,T细胞对B细胞的辅助作用由T细胞替代因子(TRF)介导或通过T细胞与B细胞的直接相互作用(同源相互作用)来实现。当用针对TRF受体位点的DCF1雄性抗BALB / c - B IgG抗体的生物素化F(ab')2片段预处理DNP - KLH致敏的脾B细胞,随后用抗生物素蛋白 - RA处理,在单克隆TRF存在下用DNP - OVA刺激时,抗DNP PFC反应显著降低,而相同处理的B细胞在Tbc致敏的T细胞存在下(同源相互作用)对DNP - PPD刺激反应良好。这些结果表明,负责同源相互作用的B细胞和具有TRF受体位点的B细胞属于不同的B细胞亚群,并且由生物素化抗体和抗生物素蛋白 - RA通过抗生物素蛋白 - 生物素复合物形成的抗体与RA的非共价偶联物的杀细胞作用具有免疫选择性,仅消除被该抗体识别的后一个B细胞亚群。