Srivastava Pramod K
Center for Immunotherapy of Cancer and Infectious Diseases, Department of Immunology, University of Connecticut School of Medicine, Farmington, CT 06030-1601, USA.
Curr Opin Immunol. 2006 Apr;18(2):201-5. doi: 10.1016/j.coi.2006.01.009. Epub 2006 Feb 7.
The immunological bases of current approaches to therapeutic cancer vaccination (or 'vacci-treatment') have been established for a decade or longer. The new developments lie mostly in the lessons learnt from clinical testing of these approaches. Three lessons are particularly worthy of note. First, recently completed randomized Phase 3 trials suggest that vacci-treatment with autologous dendritic cells expressing prostatic acid phosphatase (for prostate cancer) or with autologous tumor-derived heat shock protein (gp96)-peptide complexes show promise in enhancing survival of cancer patients. These two approaches are undergoing further randomized clinical testing. Second, immunological monitoring of many clinical trials has failed to identify a surrogate marker for clinical outcomes. Finally, an increasing volume of literature suggests that protective immunity to human cancers is elicited by the mutated antigenic repertoire unique to each cancer.
当前治疗性癌症疫苗接种(或“疫苗治疗”)方法的免疫学基础已经确立了十年或更长时间。新进展主要在于从这些方法的临床试验中吸取的经验教训。有三点经验教训尤其值得注意。第一,最近完成的随机3期试验表明,用表达前列腺酸性磷酸酶的自体树突状细胞(用于前列腺癌)或用自体肿瘤衍生的热休克蛋白(gp96)-肽复合物进行疫苗治疗在提高癌症患者生存率方面显示出前景。这两种方法正在进行进一步的随机临床试验。第二,许多临床试验的免疫监测未能确定临床结果的替代标志物。最后,越来越多的文献表明,对人类癌症的保护性免疫是由每种癌症特有的突变抗原库引发的。