Saito M, Yamazaki M, Mizuno D
Gan. 1978 Jun;69(3):331-7.
Humoral and cellular immune responses were investigated after combination therapy with syngeneic antitumor serum and bacterial lipopolysaccharide (LPS). The titer of antitumor antibody determined by using a macrophage-mediated system was very high in mice cured by the combination therapy, and this high titer lasted for a long time. In contrast, no significant titer was detected using an antibody-dependent lymphocyte-mediated system. Thus, antibody-dependent macrophage-mediated cytolysis was a more sensitive method for detecting antitumor antibody. The cellular immune response was measured as the delayed hypersensitivity reaction to tumor cells. In mice that had been cured by combination therapy, this reaction appeared at an early stage, before any antitumor antibody was detectable, but it soon decreased. On the other hand, tumor-bearing mice showed a low level of antibody and no significant delayed hypersensitivity reaction.
在同基因抗肿瘤血清与细菌脂多糖(LPS)联合治疗后,对体液免疫和细胞免疫反应进行了研究。通过巨噬细胞介导系统测定的抗肿瘤抗体效价在联合治疗治愈的小鼠中非常高,且这种高效价持续了很长时间。相比之下,使用抗体依赖淋巴细胞介导系统未检测到明显的效价。因此,抗体依赖巨噬细胞介导的细胞溶解是检测抗肿瘤抗体更敏感的方法。细胞免疫反应通过对肿瘤细胞的迟发型超敏反应来衡量。在联合治疗治愈的小鼠中,这种反应在可检测到任何抗肿瘤抗体之前的早期阶段就出现了,但很快就下降了。另一方面,荷瘤小鼠抗体水平较低,且没有明显的迟发型超敏反应。