Gupta Richa, Emens Leisha A
Department of Oncology and The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, 1650 Orleans Street, Baltimore, Maryland 21231, USA.
Discov Med. 2010 Jul;10(50):52-60.
Cancer vaccines consisting of intact tumor cells genetically modified to secrete the cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) have undergone extensive preclinical development. These vaccines induce the massive accumulation of dendritic cells at the intradermal injection site, which engulf, process, and present tumor antigens to activate tumor-specific T cells. Early phase clinical testing demonstrated promising evidence of safety and bioactivity, although initial phase III clinical trials were unsuccessful. Together, the preclinical and clinical data argue for the continued clinical development of these vaccines, integrating them with standard and novel cancer therapeutics that enhance vaccine activity by overcoming immune tolerance and suppression, and/or augmenting co-stimulatory pathways of T cell activation.
由经过基因改造以分泌细胞因子粒细胞巨噬细胞集落刺激因子(GM-CSF)的完整肿瘤细胞组成的癌症疫苗已经历了广泛的临床前开发。这些疫苗可诱导树突状细胞在皮内注射部位大量聚集,这些树突状细胞吞噬、处理并呈递肿瘤抗原以激活肿瘤特异性T细胞。早期临床试验显示出了有前景的安全性和生物活性证据,尽管最初的III期临床试验未成功。综合临床前和临床数据表明,这些疫苗应继续进行临床开发,并将它们与标准和新型癌症治疗方法相结合,通过克服免疫耐受和抑制,和/或增强T细胞激活的共刺激途径来增强疫苗活性。