Durrant L G, Spendlove I
CRUK Department of Clinical Oncology, University of Nottingham, City Hospital, Nottingham, NG5 1PB, UK.
Expert Opin Emerg Drugs. 2003 Nov;8(2):489-500. doi: 10.1517/14728214.8.2.489.
The last 10 years have seen a growth in the number of tumour antigens identified from immune responses raised in patients. The discovery that tumours can be recognised by the immune system stimulated a great deal of work characterising the molecular mechanisms underlying immune recognition. This in turn has led to an impressive array of immunological approaches to the generation of cancer vaccines; these range from molecularly defined T cell epitopes, antibody-based vaccines, cytokine therapies, immune modulators and DNA vaccines, to whole cell vaccines and, more recently, combinations of these methods. Many of these approaches have entered Phase I/II trials and have shown interesting clinical results. Moreover, they have extended our knowledge of the immune system and our understanding of the mechanisms required to design a successful cancer vaccine. This review outlines some of the approaches that have led to some of these vaccines entering Phase III clinical trials, discusses their modes of action and reports on their current status in trial.
在过去十年中,从患者体内引发的免疫反应中识别出的肿瘤抗原数量有所增加。肿瘤可被免疫系统识别这一发现激发了大量工作,以表征免疫识别背后的分子机制。这进而催生了一系列令人瞩目的免疫方法来研发癌症疫苗;这些方法包括分子定义的T细胞表位、基于抗体的疫苗、细胞因子疗法、免疫调节剂和DNA疫苗,乃至全细胞疫苗,以及最近这些方法的组合。其中许多方法已进入I/II期试验,并展现出了有趣的临床结果。此外,它们拓展了我们对免疫系统的认识,以及我们对设计成功癌症疫苗所需机制的理解。本综述概述了一些已使部分此类疫苗进入III期临床试验的方法,讨论了它们的作用模式,并报告了它们目前的试验状态。