Bartlett G L, Kreider J W, Purnell D M
Int J Cancer. 1979 Nov 15;24(5):629-35. doi: 10.1002/ijc.2910240517.
This report describes a new animal model for active, specific, systemic immunotherapy of leukemia. Mice were challenged (day 0) with 10(3) viable LSTRA cells and treated later with a vaccine containing 10(7) irradiated LSTRA cells. Four intraperitoneal or intravenous vaccine injections, on days 2, 9, 16 and 23, caused significant prolongation of survival; single injections by the same routes had inconsistent effects. Vaccine was not effective against a higher initial challenge dose, when given later in the course of tumor growth, when given intradermally or when used in weanling mice. The therapeutic effect was specific since a vaccine composed of an antigenically unrelated leukemia was ineffective. These results suggest that LSTRA is suitable for studying active, systemic, specific immunotherapy.
本报告描述了一种用于白血病主动、特异性、全身免疫治疗的新动物模型。在第0天用10³个活的LSTRA细胞对小鼠进行攻击,随后用含有10⁷个经辐照的LSTRA细胞的疫苗进行治疗。在第2、9、16和23天进行四次腹腔内或静脉内疫苗注射可显著延长生存期;通过相同途径进行单次注射的效果不一致。当在肿瘤生长过程后期给药、皮内给药或用于断奶小鼠时,疫苗对更高的初始攻击剂量无效。治疗效果具有特异性,因为由抗原性不相关的白血病组成的疫苗无效。这些结果表明LSTRA适合用于研究主动、全身、特异性免疫治疗。