Enker W E, Jacobitz J L
Surgery. 1976 Aug;80(2):164-70.
Active-specific immunotherapy with concanavalin A or with neuraminidase-modified syngeneic tumor cells has been studied in an experimental model of colon cancer. Systemic immunotherapy with concanavalin A-modified tumor cells or with neuraminidase-modified tumor cells has resulted in up to 70 percent cure of rats receiving a lethal inoculum of tumor in a model tumor system which otherwise proved 80 percent lethal to untreated hosts. The possible mechanisms whereby neuraminidase or concanavalin A are effective cell-surface modifiers for active-specific immunotherapy are discussed. In vitro studies suggest markedly heightened antigenic recognition following immunization with concanvalin A-modified syngeneic tumor cells. These studies represent the first apparent evidence for the definitive value of systemic active-specific immunotherapy for the adjuvant treatment of large bowel cancer.
在结肠癌的实验模型中,对伴刀豆球蛋白A或神经氨酸酶修饰的同基因肿瘤细胞进行主动特异性免疫治疗已得到研究。在一个模型肿瘤系统中,用伴刀豆球蛋白A修饰的肿瘤细胞或神经氨酸酶修饰的肿瘤细胞进行全身免疫治疗,可使接受致死剂量肿瘤接种的大鼠的治愈率高达70%,而该模型肿瘤系统对未治疗的宿主的致死率为80%。文中讨论了神经氨酸酶或伴刀豆球蛋白A作为主动特异性免疫治疗有效细胞表面修饰剂的可能机制。体外研究表明,用伴刀豆球蛋白A修饰的同基因肿瘤细胞免疫后,抗原识别明显增强。这些研究首次明确证明了全身主动特异性免疫治疗在辅助治疗大肠癌方面的明确价值。