Janikashvili Nona, Larmonier Nicolas, Katsanis Emmanuel
Department of Pediatrics, Steele Children's Research Center, Arizona 85724, USA.
Immunotherapy. 2010 Jan;2(1):57-68. doi: 10.2217/imt.09.78.
Advances in the understanding of the immunoregulatory functions of dendritic cells (DCs) in animal models and humans have led to their exploitation as anticancer vaccines. Although DC-based immunotherapy has proven clinically safe and efficient to induce tumor-specific immune responses, only a limited number of objective clinical responses have been reported in cancer patients. These relatively disappointing results have prompted the evaluation of multiple approaches to improve the efficacy of DC vaccines. The topic of this review focuses on personalized DC-based anticancer vaccines, which in theory have the potential to present to the host immune system the entire repertoire of antigens harbored by autologous tumor cells. We also discuss the implementation of these vaccines in cancer therapeutic strategies, their limitations and the future challenges for effective immunotherapy against cancer.
在动物模型和人类中对树突状细胞(DCs)免疫调节功能认识的进展,已促使人们将其开发为抗癌疫苗。尽管基于DC的免疫疗法已在临床上证明安全有效,可诱导肿瘤特异性免疫反应,但在癌症患者中仅报道了有限数量的客观临床反应。这些相对令人失望的结果促使人们评估多种方法以提高DC疫苗的疗效。本综述的主题聚焦于个性化的基于DC的抗癌疫苗,从理论上讲,这种疫苗有潜力向宿主免疫系统呈递自体肿瘤细胞所携带的全部抗原库。我们还将讨论这些疫苗在癌症治疗策略中的应用、它们的局限性以及有效抗癌免疫疗法未来面临的挑战。