The genetic and cellular basis of regulation of the immune response to tumor antigens.

M I Greene
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引用次数: 72

Abstract

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.

肿瘤抗原免疫反应调控的遗传和细胞基础。
在本章中,我讨论了肿瘤抗原免疫反应调控的细胞和遗传基础。我有意省略了对ADCC、NK和B细胞等效应器的讨论,因为我自己对这些效应器的经验主要涉及与小肿瘤接种相关的早期事件(Greenberg和Greene, 1976)。在该模型中,天然抗体和巨噬细胞参与的NK和ADCC机制是重要的,而T细胞则不是。在我在这里讨论的研究中,已经评估了更多的晚期肿瘤模型。很明显,我希望从本章中了解免疫细胞或t活化的途径将为未来应用免疫治疗技术提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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