Programa de Inmunología e Inmunoterapia, Centro de Investigación Médica Aplicada (CIMA), Universidad de Navarra, Pamplona, Spain.
Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Front Immunol. 2018 Sep 3;9:1923. doi: 10.3389/fimmu.2018.01923. eCollection 2018.
Understanding mechanisms associated to dendritic cell (DC) functions has allowed developing new antitumor therapeutic vaccination strategies. However, these vaccines have demonstrated limited clinical results. Although the low immunogenicity of tumor antigens used and the presence of tumor-associated suppressive factors may in part account for these results, intrinsic vaccine-related factors may also be involved. Vaccines modulate DC functions by inducing activating and inhibitory signals that determine ensuing T cell responses. In this mini review, we focus on IL-10, inhibitory cytokine induced in DC upon vaccination, which defines a suppressive cell subset, discussing its implications as a potential target in combined vaccination immunotherapies.
了解与树突状细胞 (DC) 功能相关的机制,使得开发新的抗肿瘤治疗性疫苗策略成为可能。然而,这些疫苗的临床效果有限。虽然所使用的肿瘤抗原的低免疫原性和肿瘤相关抑制因子的存在可能部分解释了这些结果,但内在的疫苗相关因素也可能涉及其中。疫苗通过诱导激活和抑制信号来调节 DC 功能,这些信号决定了随后的 T 细胞反应。在这篇综述中,我们重点讨论了 IL-10,即接种疫苗后 DC 诱导产生的抑制性细胞因子,它定义了一个抑制性细胞亚群,并讨论了其作为联合疫苗免疫治疗的潜在靶点的意义。