Kataoka T
Gan To Kagaku Ryoho. 1986 Mar;13(3 Pt 2):701-5.
6-Mercaptopurine inhibited suppressor macrophages and induced antitumor monocytes in L1210-bearing mice. Although these antitumor monocytes did not neutralize L1210, they augmented the antitumor response in L1210 vaccine-primed recipient mice against a subsequent inoculation of live L1210. These results led to the trial of a novel immunochemotherapy regimen in which L1210 vaccine and 6-mercaptopurine in combination produced a synergistic therapeutic effect. In contrast, cyclophosphamide did not inhibit suppressor macrophages, nor did it induce antitumor monocytes in L1210-bearing mice. Consequently, the combination of L1210 vaccine and cyclophosphamide did not produce any further improvement in therapy. These results showed that modulation of macrophages and monocytes was associated with immunotherapeutic effect.
6-巯基嘌呤抑制了荷L1210小鼠体内的抑制性巨噬细胞,并诱导出抗肿瘤单核细胞。虽然这些抗肿瘤单核细胞不能中和L1210,但它们增强了经L1210疫苗致敏的受体小鼠对随后接种的活L1210的抗肿瘤反应。这些结果促成了一种新型免疫化疗方案的试验,其中L1210疫苗和6-巯基嘌呤联合使用产生了协同治疗效果。相比之下,环磷酰胺既不抑制荷L1210小鼠体内的抑制性巨噬细胞,也不诱导抗肿瘤单核细胞。因此,L1210疫苗和环磷酰胺联合使用在治疗上并未产生任何进一步的改善。这些结果表明,巨噬细胞和单核细胞的调节与免疫治疗效果相关。