Haubeck H D, Kölsch E
Immunology. 1982 Nov;47(3):503-10.
Initial stages of tumour growth are not easily accessible to investigation. Therefore an experimental procedure was developed to mimic tumorigenesis as closely as possible. BALB/c mice received intraperitoneally exponentially increasing numbers of irradiated syngeneic ADJ-PC-5 plasmacytoma cells. The initial injection began with two cells per mouse and according to the generation time of this tumour, subsequent doses were doubled until mice had received up to 10(5) tumour cells. At various stages of treatment, peritoneal exudate cells (PEC) and spleen cells (SC) were tested for either cytotoxicity or specific suppression of induction of a primary in vitro T-cell cytotoxic response (CTL) of BALB/c spleen cells against ADJ-PC-5 plasmacytoma cells. No cytotoxic PEC were found. Instead, PEC from mice in which the final tumour cells number had reached or exceeded 10(3) irradiated ADJ-PC-5 cells, induced complete suppression of this primary in vitro CTL. Specificity was found both in the induction and effector phase of suppression. Specific suppression was mediated by Thy-1.2+ cells and amplified by non-specific suppression through adherent cells. The data arae discussed in context with previous findings on the in vivo immunogenicity and tolerogenicity of the ADJ-PC-5 plasmacytoma. They suggest that induction of T suppressor (Ts) cells might be an early event in tumorigenesis.
肿瘤生长的初始阶段不易进行研究。因此,开发了一种实验程序,以尽可能紧密地模拟肿瘤发生过程。BALB/c小鼠腹腔内注射数量呈指数增加的经照射的同基因ADJ-PC-5浆细胞瘤细胞。初始注射为每只小鼠注射两个细胞,根据该肿瘤的生成时间,随后的剂量加倍,直到小鼠接受多达10(5)个肿瘤细胞。在治疗的不同阶段,检测腹腔渗出细胞(PEC)和脾细胞(SC)对BALB/c脾细胞针对ADJ-PC-5浆细胞瘤细胞的原发性体外T细胞细胞毒性反应(CTL)的诱导的细胞毒性或特异性抑制作用。未发现具有细胞毒性的PEC。相反,最终肿瘤细胞数量达到或超过10(3)个经照射的ADJ-PC-5细胞的小鼠的PEC,诱导了对这种原发性体外CTL的完全抑制。在抑制的诱导和效应阶段均发现了特异性。特异性抑制由Thy-1.2+细胞介导,并通过黏附细胞的非特异性抑制作用放大。结合先前关于ADJ-PC-5浆细胞瘤体内免疫原性和耐受性的研究结果对这些数据进行了讨论。这些结果表明,T抑制(Ts)细胞的诱导可能是肿瘤发生过程中的早期事件。