Werkmeister J A, Burns G F, Triglia T
J Immunol. 1984 Sep;133(3):1385-90.
We previously described a monoclonal antibody, 9.1C3, which blocked natural killer (NK) cell-mediated cytolysis by acting on effector cells during a late step in the lethal hit stage. The present work describes the production in rabbits of anti-idiotypic (anti-id) antibodies to the 9.1C3 antibody. In addition to reacting specifically with the 9.1C3 antibody, the anti-id antibodies bound strongly to the K562 target cell. The anti-id antibodies blocked killing of K562 targets by NK, antibody-dependent cellular cytotoxicity, and NK-like cells but did not inhibit killing by cytotoxic T lymphocytes (CTL). Pretreatment of cells and washing before assay indicated that blocking occurred at the target cell level. Of particular interest, single cell assays with Percoll-enriched large granular lymphocytes demonstrated that the antibodies caused no reduction in binding. These data are consistent with a model for NK cell-mediated lysis that involves a secondary target cell receptor independent of the primary NK-target cell interaction. The anti-id antibodies immunoprecipitated cell surface proteins of relative m.w. 79K and 62K unreduced, and 94K and 79K reduced from K562 target cells. The development of anti-id antibodies may be a useful procedure to explore the structure and function of cellular receptors involved in NK cell-mediated cytolysis.
我们之前描述过一种单克隆抗体9.1C3,它在致死性打击阶段的后期作用于效应细胞,从而阻断自然杀伤(NK)细胞介导的细胞溶解作用。目前的研究描述了在兔体内产生针对9.1C3抗体的抗独特型(抗Id)抗体。除了与9.1C3抗体发生特异性反应外,抗Id抗体还能与K562靶细胞强烈结合。抗Id抗体可阻断NK细胞、抗体依赖性细胞毒性以及NK样细胞对K562靶细胞的杀伤作用,但不抑制细胞毒性T淋巴细胞(CTL)的杀伤作用。在检测前对细胞进行预处理和洗涤表明,阻断作用发生在靶细胞水平。特别值得关注的是,用Percoll富集的大颗粒淋巴细胞进行的单细胞检测表明,这些抗体不会减少结合。这些数据与NK细胞介导的裂解模型一致,该模型涉及一种独立于主要NK-靶细胞相互作用的二级靶细胞受体。抗Id抗体免疫沉淀了K562靶细胞中相对分子质量未还原时为79K和62K、还原后为94K和79K的细胞表面蛋白。抗Id抗体的产生可能是探索参与NK细胞介导的细胞溶解作用的细胞受体结构和功能的一种有用方法。