Domagala Joanna, Lachota Mieszko, Klopotowska Marta, Graczyk-Jarzynka Agnieszka, Domagala Antoni, Zhylko Andriy, Soroczynska Karolina, Winiarska Magdalena
Department of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Postgraduate School of Molecular Medicine, Medical University of Warsaw, 02-091 Warsaw, Poland.
Cancers (Basel). 2020 Nov 27;12(12):3542. doi: 10.3390/cancers12123542.
NK cells have unique capabilities of recognition and destruction of tumor cells, without the requirement for prior immunization of the host. Maintaining tolerance to healthy cells makes them an attractive therapeutic tool for almost all types of cancer. Unfortunately, metabolic changes associated with malignant transformation and tumor progression lead to immunosuppression within the tumor microenvironment, which in turn limits the efficacy of various immunotherapies. In this review, we provide a brief description of the metabolic changes characteristic for the tumor microenvironment. Both tumor and tumor-associated cells produce and secrete factors that directly or indirectly prevent NK cell cytotoxicity. Here, we depict the molecular mechanisms responsible for the inhibition of immune effector cells by metabolic factors. Finally, we summarize the strategies to enhance NK cell function for the treatment of tumors.
自然杀伤(NK)细胞具有识别和破坏肿瘤细胞的独特能力,无需预先对宿主进行免疫接种。对健康细胞保持耐受性使其成为几乎所有类型癌症颇具吸引力的治疗工具。不幸的是,与恶性转化和肿瘤进展相关的代谢变化会导致肿瘤微环境内的免疫抑制,进而限制各种免疫疗法的疗效。在本综述中,我们简要描述了肿瘤微环境特有的代谢变化。肿瘤细胞和肿瘤相关细胞都会产生并分泌直接或间接阻止NK细胞细胞毒性的因子。在此,我们描述了代谢因子抑制免疫效应细胞的分子机制。最后,我们总结了增强NK细胞功能以治疗肿瘤的策略。