Department of Immunogenetics, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, 860-8556, Japan.
Semin Immunopathol. 2011 Nov;33(6):603-12. doi: 10.1007/s00281-011-0263-y. Epub 2011 Apr 5.
In vivo transfer of dendritic cells (DC) has proven efficient in the priming of T cells and is regarded as a powerful means of providing anti-cancer immunotherapy. Clinical trials of anti-cancer therapy with DC pulsed with peptide antigens have been carried out in many institutions, although dramatic therapeutic effect has not been observed in most of the trials. Negative regulation of the immune response by DC might be applicable to treatment of autoimmune diseases and transplantation medicine. Currently, the DC used for anti-cancer vaccine therapy are generated from the peripheral blood monocytes of the patients. However, there is a limitation in the number of available monocytes and the potential of monocytes to differentiate into DC varies depending on the individual blood donors. To resolve the issue of the cell source for DC therapy, several groups have developed methods to generate DC from pluripotent stem cells. This review introduces methods to generate functional DC from pluripotent stem cells of mouse and human.
树突状细胞(DC)体内转移已被证明能有效地激活 T 细胞,被认为是提供抗癌免疫疗法的有力手段。许多机构已经开展了用肽抗原冲击树突状细胞的抗癌治疗的临床试验,尽管在大多数试验中并未观察到显著的治疗效果。DC 对免疫反应的负调控可能适用于治疗自身免疫性疾病和移植医学。目前,用于抗癌疫苗治疗的 DC 是从患者的外周血单核细胞中产生的。然而,可用单核细胞的数量有限,并且单核细胞分化为 DC 的潜力因个体供体而异。为了解决 DC 治疗的细胞来源问题,一些研究小组已经开发了从多能干细胞生成 DC 的方法。这篇综述介绍了从鼠和人多能干细胞生成功能性 DC 的方法。