Greene M I
Contemp Top Immunobiol. 1980;11:81-116. doi: 10.1007/978-1-4684-3701-0_2.
In this chapter I have dealt with the cellular and genetic basis of regulation of the immune response to tumor antigen. I have knowingly omitted discussion of effectors such as ADCC, NK, and B cells, since my own experience with such effectors relates primarily to early events associated with small-tumor inocula (Greenberg and Greene, 1976). In that model, NK and ADCC mechanisms, in which natural antibody and macrophages participate, are of importance and T cells are not. In the studies I have dealt with herein, more advanced tumor models have been evaluated. It is clear, I hope, from this chapter that understanding the pathways to immune-cell or Ts activation will provide the basis for applied immunotherapy techniques in the future.
在本章中,我探讨了针对肿瘤抗原的免疫反应调节的细胞和遗传基础。我有意省略了对诸如抗体依赖的细胞介导的细胞毒性作用(ADCC)、自然杀伤细胞(NK)和B细胞等效应细胞的讨论,因为我自己对这些效应细胞的研究主要涉及与小肿瘤接种相关的早期事件(格林伯格和格林,1976年)。在那个模型中,自然抗体和巨噬细胞参与的NK和ADCC机制很重要,而T细胞则不然。在我在此处论述的研究中,已经评估了更先进的肿瘤模型。我希望,从本章可以清楚地看出,了解免疫细胞或抑制性T细胞(Ts)激活的途径将为未来的应用免疫治疗技术提供基础。