Lamberti María Julia, Nigro Annunziata, Mentucci Fátima María, Rumie Vittar Natalia Belén, Casolaro Vincenzo, Dal Col Jessica
Departamento de Biología Molecular, Universidad Nacional de Río Cuarto, Río Cuarto 5800, Córdoba, Argentina.
INBIAS, CONICET-UNRC, Río Cuarto 5800, Córdoba, Argentina.
Pharmaceutics. 2020 Mar 12;12(3):256. doi: 10.3390/pharmaceutics12030256.
The safety and feasibility of dendritic cell (DC)-based immunotherapies in cancer management have been well documented after more than twenty-five years of experimentation, and, by now, undeniably accepted. On the other hand, it is equally evident that DC-based vaccination as monotherapy did not achieve the clinical benefits that were predicted in a number of promising preclinical studies. The current availability of several immune modulatory and targeting approaches opens the way to many potential therapeutic combinations. In particular, the evidence that the immune-related effects that are elicited by immunogenic cell death (ICD)-inducing therapies are strictly associated with DC engagement and activation strongly support the combination of ICD-inducing and DC-based immunotherapies. In this review, we examine the data in recent studies employing tumor cells, killed through ICD induction, in the formulation of anticancer DC-based vaccines. In addition, we discuss the opportunity to combine pharmacologic or physical therapeutic approaches that can promote ICD in vivo with in situ DC vaccination.
经过二十五年多的实验,基于树突状细胞(DC)的免疫疗法在癌症治疗中的安全性和可行性已有充分记录,并且目前已无可争议地被接受。另一方面,同样明显的是,作为单一疗法的基于DC的疫苗接种并未实现许多有前景的临床前研究所预测的临床益处。目前多种免疫调节和靶向方法的出现为许多潜在的治疗组合开辟了道路。特别是,由诱导免疫原性细胞死亡(ICD)的疗法引发的免疫相关效应与DC的参与和激活密切相关,这一证据有力地支持了诱导ICD的疗法与基于DC的免疫疗法的联合应用。在这篇综述中,我们研究了近期使用通过诱导ICD杀死的肿瘤细胞来制备抗癌DC疫苗的研究数据。此外,我们还讨论了将能够在体内促进ICD的药物或物理治疗方法与原位DC疫苗接种相结合的机会。