Department of Pediatric Haematology/Oncology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.
Department of Pediatric Haematology/Oncology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy; Department of Pediatric Sciences, University of Pavia, Pavia, Italy.
Trends Mol Med. 2017 Dec;23(12):1156-1175. doi: 10.1016/j.molmed.2017.10.002. Epub 2017 Nov 10.
Natural killer (NK) cells efficiently recognize and kill tumor cells through several mechanisms including the expression of ligands for NK cell-activating receptors on target cells. Different clinical trials indicate that NK cell-based immunotherapy represents a promising antitumor treatment. However, tumors develop immune-evasion strategies, including downregulation of ligands for NK cell-activating receptors, that can negatively affect antitumor activity of NK cells, which either reside endogenously, or are adoptively transferred. Thus, restoration of the expression of NK cell-activating ligands on tumor cells represents a strategic therapeutic goal. As discussed here, various anticancer drugs can fulfill this task via different mechanisms. We envision that the combination of selected chemotherapeutic agents with NK cell adoptive transfer may represent a novel strategy for cancer immunotherapy.
自然杀伤 (NK) 细胞通过多种机制有效地识别和杀死肿瘤细胞,包括在靶细胞上表达 NK 细胞激活受体的配体。不同的临床试验表明,基于 NK 细胞的免疫疗法代表了一种有前途的抗肿瘤治疗方法。然而,肿瘤会发展出免疫逃逸策略,包括下调 NK 细胞激活受体的配体,这可能会对 NK 细胞的抗肿瘤活性产生负面影响,这些 NK 细胞要么内源性存在,要么被过继转移。因此,恢复肿瘤细胞上 NK 细胞激活配体的表达是一个战略治疗目标。如这里所讨论的,各种抗癌药物可以通过不同的机制来实现这一目标。我们设想,将选定的化疗药物与 NK 细胞过继转移相结合可能代表癌症免疫治疗的一种新策略。