Takakura Kazuki, Kajihara Mikio, Ito Zensho, Ohkusa Toshifumi, Gong Jianlin, Koido Shigeo
Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine; and Institute of Clinical Medicine and Research; The Jikei University School of Medicine, Tokyo, Japan.
Discov Med. 2015 Mar;19(104):169-74.
A promising area of clinical investigation is the use of cancer immunotherapy to treat cancer patients. Dendritic cells (DCs) operate as professional antigen-presenting cells (APCs) and play a critical role in the induction of antitumor immune responses. Thus, DC-based cancer immunotherapy represents a powerful strategy. One DC-based cancer immunotherapy strategy that has been investigated is the administration of fusion cells generated with DCs and whole tumor cells (DC-tumor fusion cells). The DC-tumor fusion cells can process a broad array of tumor-associated antigens (TAAs), including unidentified molecules, and present them through major histocompatibility complex (MHC) class I and II pathways in the context of co-stimulatory signals. Improving the therapeutic efficacy of DC-tumor fusion cell-based cancer immunotherapy requires increased immunogenicity of DCs and whole tumor cells. We discuss the potential ability of DC-tumor fusion cells to activate antigen-specific T cells and strategies to improve the immunogenicity of DC-tumor fusion cells as anticancer vaccines.
临床研究中一个很有前景的领域是使用癌症免疫疗法来治疗癌症患者。树突状细胞(DCs)作为专职抗原呈递细胞(APCs)发挥作用,在诱导抗肿瘤免疫反应中起关键作用。因此,基于DC的癌症免疫疗法是一种强大的策略。一种已被研究的基于DC的癌症免疫疗法策略是给予由DC和完整肿瘤细胞生成的融合细胞(DC-肿瘤融合细胞)。DC-肿瘤融合细胞可以处理广泛的肿瘤相关抗原(TAAs),包括未识别的分子,并在共刺激信号的背景下通过主要组织相容性复合体(MHC)I类和II类途径呈递它们。提高基于DC-肿瘤融合细胞的癌症免疫疗法的治疗效果需要增强DC和完整肿瘤细胞的免疫原性。我们讨论了DC-肿瘤融合细胞激活抗原特异性T细胞的潜在能力以及提高DC-肿瘤融合细胞作为抗癌疫苗的免疫原性的策略。