Romani L, Fioretti M C, Bonmassar E
Transplantation. 1979 Sep;28(3):218-22. doi: 10.1097/00007890-197909000-00013.
Drug-mediated tumor antigens (DMTA), which appear after in vivo treatment of murine lymphomas with 5-(3,3'-dimethyl-1-triazeno)-imidazole-4-carboxamide (DTIC), are shown to elicit strong primary cell-mediated responses in vitro. Specific cytotoxic response is obtained using CD2F1 (H-2d/H-2d) spleen cells cocultured in vitro for 5 days with inactivated histocompatible L5178Y/DTIC lymphoma cells in a one-way mixed lymphocyte tumor culture. Sensitized lymphoid cells are markedly cytotoxic for L5178Y/DTIC targets and are minimally or not active against the parental lymphoma. Marginal or no cross-reactivity is found between L5178Y/DTIC lymphoma and other untreated or DTIC-treated tumor or normal cells. Cytotoxic activity is T dependent, since it is abrogated by treatment in vitro with anti-serum and complement and is not elicited by spleen cells of athymic (nude) donors.
在用5-(3,3'-二甲基-1-三氮烯基)-咪唑-4-甲酰胺(DTIC)对小鼠淋巴瘤进行体内治疗后出现的药物介导肿瘤抗原(DMTA),在体外可引发强烈的原发性细胞介导反应。在单向混合淋巴细胞肿瘤培养中,使用CD2F1(H-2d/H-2d)脾细胞与灭活的组织相容性L5178Y/DTIC淋巴瘤细胞在体外共培养5天,可获得特异性细胞毒性反应。致敏淋巴细胞对L5178Y/DTIC靶细胞具有明显的细胞毒性,而对亲代淋巴瘤的活性最低或无活性。在L5178Y/DTIC淋巴瘤与其他未处理或经DTIC处理的肿瘤或正常细胞之间发现边缘性或无交叉反应性。细胞毒性活性是T细胞依赖性的,因为它可被体外抗血清和补体处理所消除,且无胸腺(裸)供体的脾细胞不会引发这种活性。