Vile R G, Chong H
Imperial Cancer Research Fund Laboratory of Cancer Gene Therapy, St. Thomas' Hospital, London, UK.
Cancer Metastasis Rev. 1996 Sep;15(3):351-64. doi: 10.1007/BF00046347.
Animal models have clearly shown that tumor cells may be amenable to molecular manipulation which can result in immune activation and rejection of unmodified cells (Chapters 4 and 5). The challenge now is to design clinical trials which have a realistic chance of success, (although the definition of 'success' is itself an important issue [see Chapter 9]. How should such a strategy be formulated? A review of the previous fifteen years since the first (immune) gene transfer studies were reported, encompasses a great wealth of data. Unfortunately, far from crystallising a set of unifying principles, these diverse reports shroud us in a fog of uncertainty as to how best to proceed. However, if this technology is to have practical, widespread application in the treatment of cancer patients, it is necessary to identify certain critical immunological goals which any protocols should achieve. Clear elucidation of these goals, by unifying the huge amount of disparate experimental data, must eventually be accomplished. In this chapter, we have reviewed the literature covering the era of molecular immunotherapy. We propose four general goals around which widely applicable clinical protocols, not necessarily dependent upon tumour type or experimental bias, might be based and suggest how they may be achieved in the context of gene transfer.
动物模型已清楚表明,肿瘤细胞可能适于进行分子操作,这种操作可导致免疫激活并排斥未修饰的细胞(见第4章和第5章)。当前面临的挑战是设计出有切实成功机会的临床试验(尽管“成功”的定义本身就是一个重要问题[见第9章])。应如何制定这样的策略呢?回顾自首次报道(免疫)基因转移研究以来的过去十五年,可获得大量数据。遗憾的是,这些不同的报告远未形成一套统一的原则,反而让我们在如何最佳推进方面陷入了不确定的迷雾之中。然而,如果这项技术要在癌症患者治疗中得到实际广泛应用,就有必要确定任何方案都应实现的某些关键免疫学目标。通过整合大量不同的实验数据来清晰阐明这些目标,最终必定能够实现。在本章中,我们回顾了涵盖分子免疫治疗时代的文献。我们提出了四个总体目标,广泛适用的临床方案(不一定依赖于肿瘤类型或实验偏差)可能基于这些目标,并说明了在基因转移的背景下如何实现这些目标。