Hamilton Gerhard, Plangger Adelina
Department of Vascular Surgery, Medical University of Vienna, Vienna, Austria.
Biologics. 2021 Jul 7;15:265-277. doi: 10.2147/BTT.S290305. eCollection 2021.
Lung cancer has a dismal prognosis and novel targeted therapies leave still room for major improvements and better outcomes. Immunotherapy targeting immune checkpoint (IC) proteins, either as single agents or in combination with chemotherapy, is active but responders constitute only approximately 10-15% of non-small cell lung cancer (NSCLC) patients. Other effector immune cells such as CAR-T cells or NK cells may help to overcome the limitations of the IC inhibitor therapies for lung cancer. NK cells can kill tumor cells without previous priming and are present in the circulatory system and lymphoid organs. Tissue-residing NK cells differ from peripheral effector cells and, in case of the lung, comprise CD56bright CD16-negative populations showing high cytokine release but low cytotoxicity in contrast to the circulating CD56dim CD16-positive NK cells exhibiting high cytotoxic efficacy. This local attenuation of NK cell killing potency seems due to a specific stage of NK differentiation, immunosuppressive factors as well as presence of myeloid-derived suppressor cells (MDSCs) and regulatory T cells (TREGs). Improved NK cell-based immunotherapies involve IL-2-stimulated effector cells, NK cells expanded with the help of cytokines, permanent NK cell lines, induced pluripotent stem cell-derived NK cells and NK cells armed with chimeric antigen receptors. Compared to CAR T cell therapy, NK cells administration is devoid of graft-versus-host disease (GvHD) and cytokine-release syndrome. Although NK cells are clearly active against lung cancer cells, the low-cytotoxicity differentiation state in lung tumors, the presence of immunosuppressive leucocyte populations, limited infiltration and adverse conditions of the microenvironment need to be overcome. This goal may be achieved in the future using large numbers of activated and armed NK cells as provided by novel methods in NK cell isolation, expansion and stimulation of cytotoxic activity, including combinations with monoclonal antibodies in antibody-dependent cytotoxicity (ADCC). This review discusses the basic characteristics of NK cells and the potential of NK cell preparations in cancer therapy.
肺癌的预后不佳,新型靶向治疗仍有很大的改进空间以实现更好的治疗效果。针对免疫检查点(IC)蛋白的免疫疗法,无论是单药治疗还是与化疗联合使用,都具有活性,但应答者仅占非小细胞肺癌(NSCLC)患者的约10 - 15%。其他效应免疫细胞,如嵌合抗原受体T细胞(CAR-T细胞)或自然杀伤细胞(NK细胞),可能有助于克服IC抑制剂治疗肺癌的局限性。NK细胞无需预先致敏就能杀伤肿瘤细胞,存在于循环系统和淋巴器官中。组织驻留NK细胞与外周效应细胞不同,就肺部而言,包括CD56bright CD16阴性群体,与循环中的CD56dim CD16阳性NK细胞相比,它们具有高细胞因子释放但低细胞毒性,而后者具有高细胞毒性效力。NK细胞杀伤能力的这种局部减弱似乎是由于NK细胞分化的特定阶段、免疫抑制因子以及髓系来源的抑制细胞(MDSC)和调节性T细胞(TREG)的存在。改进的基于NK细胞的免疫疗法包括白细胞介素-2刺激的效应细胞、在细胞因子帮助下扩增的NK细胞、永久性NK细胞系、诱导多能干细胞衍生的NK细胞以及配备嵌合抗原受体的NK细胞。与CAR-T细胞疗法相比,NK细胞给药不会引发移植物抗宿主病(GvHD)和细胞因子释放综合征。尽管NK细胞对肺癌细胞有明显的活性,但需要克服肺部肿瘤中低细胞毒性的分化状态、免疫抑制白细胞群体的存在、有限的浸润以及微环境的不利条件。未来,通过新型NK细胞分离、扩增和细胞毒性活性刺激方法提供的大量活化和武装的NK细胞,包括与单克隆抗体在抗体依赖性细胞毒性(ADCC)中的联合使用,可能实现这一目标。本综述讨论了NK细胞的基本特征以及NK细胞制剂在癌症治疗中的潜力。