Bonavida B
J Exp Med. 1977 Feb 1;145(2):293-301. doi: 10.1084/jem.145.2.293.
A secondary specific cytotoxic response is obtained when lymphocytes primed in vivo to a tumor allograft are exposed to Con A in culture. The secondary cytotoxic cells generated are specific to target cells bearing antigens of the primary sensitizing cells and are qualitatively indistinguishable from the response obtained upon secondary antigenic stimulation. The cell-mediated cytotoxicity is independent of concanavalin A (Con A) and is not affected by the Con A-specific inhibitor, alpha-methyl-D-mannose pyranoside. Furthermore, cultures containing a mixture of submitogenic concentrations of Con A and stimulating antigens showed synergy and augmentation of cytotoxic activity. It is suggested that activation of prekiller cells by Con A into CTL may be mediated via the same or similar receptors normally triggered by the stimulating antigens. Functional similarities between ConA and the lymphocyte-defined antigens of the major histocompatibility complex region are discussed.
当在体内对肿瘤同种异体移植物致敏的淋巴细胞在培养中暴露于刀豆蛋白A(Con A)时,可获得二次特异性细胞毒性反应。产生的二次细胞毒性细胞对携带初次致敏细胞抗原的靶细胞具有特异性,并且在质量上与二次抗原刺激后获得的反应无法区分。细胞介导的细胞毒性独立于刀豆球蛋白A(Con A),并且不受Con A特异性抑制剂α-甲基-D-甘露糖吡喃糖苷的影响。此外,含有亚致有丝分裂浓度的Con A和刺激抗原混合物的培养物显示出协同作用和细胞毒性活性增强。有人提出,Con A将前杀伤细胞激活为细胞毒性T淋巴细胞(CTL)可能是通过与刺激抗原通常触发的相同或相似受体介导的。讨论了ConA与主要组织相容性复合体区域淋巴细胞定义抗原之间的功能相似性。