INSERM U892, Institut de Biologie, 9 quai Moncousu, 44093 Nantes Cedex 01, France.
Immunotherapy. 2009 Mar;1(2):289-302. doi: 10.2217/1750743X.1.2.289.
Much effort has been made over the last decade to use dendritic cells (DCs) in vaccines to induce specific antitumor immune responses. However, the great hope provided by in vitro and in vivo preclinical investigations was not translated to the clinic in terms of clinical efficacy. Thus, one of the challenges resides in optimizing DC-based therapy to give maximum clinical efficacy while using manufacturing processes that enable quality control and scale-up of consistent products. In this article, we review DC biology and the DC-based clinical trials performed to date and focus on the DC maturation status compatible with the goals of cancer immunotherapy. We also highlight the different approaches used in these clinical studies, such as the DC types or subtypes used and their preparation. Finally, we discuss the immunological and clinical outcomes in treated patients, with emphasis on the strategies that could be used to improve DC-based vaccination.
在过去的十年中,人们付出了大量努力,希望利用树突状细胞 (DC) 疫苗来诱导特异性抗肿瘤免疫反应。然而,体外和体内临床前研究带来的巨大希望并未在临床疗效方面得到体现。因此,面临的挑战之一是优化基于树突状细胞的治疗方法,在使用能够进行质量控制和一致产品规模化生产的制造工艺的同时,实现最大的临床疗效。本文综述了树突状细胞生物学以及迄今为止开展的基于树突状细胞的临床试验,并重点关注与癌症免疫治疗目标相兼容的树突状细胞成熟状态。我们还强调了这些临床研究中使用的不同方法,例如使用的树突状细胞类型或亚型及其制备方法。最后,我们讨论了接受治疗的患者的免疫和临床结果,重点讨论了可用于改善基于树突状细胞的疫苗接种的策略。