Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche 866, France.
Cytotherapy. 2011 Aug;13(7):774-85. doi: 10.3109/14653249.2011.553593. Epub 2011 Feb 7.
Dendritic cells (DC) are professional antigen-presenting cells currently being used as a cellular adjuvant in cancer immunotherapy strategies. Unfortunately, DC-based vaccines have not demonstrated spectacular clinical results. DC loading with tumor antigens and DC differentiation and activation still require optimization. An alternative technique for providing antigens to DC consists of the direct fusion of dendritic cells with tumor cells. These resulting hybrid cells may express both major histocompatibility complex (MHC) class I and II molecules associated with tumor antigens and the appropriate co-stimulatory molecules required for T-cell activation. Initially tested in animal models, this approach has now been evaluated in clinical trials, although with limited success. We summarize and discuss the results from the animal studies and first clinical trials. We also present a new approach to inducing hybrid formation by expression of viral fusogenic membrane glycoproteins.
树突状细胞(DC)是专业的抗原呈递细胞,目前被用作癌症免疫治疗策略中的细胞佐剂。不幸的是,基于树突状细胞的疫苗并未显示出显著的临床效果。负载肿瘤抗原的树突状细胞以及树突状细胞的分化和激活仍需要优化。向树突状细胞提供抗原的另一种技术是将树突状细胞与肿瘤细胞直接融合。这些产生的杂交细胞可能表达与肿瘤抗原相关的主要组织相容性复合体(MHC)I 类和 II 类分子以及 T 细胞激活所需的适当共刺激分子。该方法最初在动物模型中进行了测试,现在已经在临床试验中进行了评估,但取得的成功有限。我们总结并讨论了动物研究和首次临床试验的结果。我们还提出了一种通过表达病毒融合膜糖蛋白诱导杂交形成的新方法。