Douka Stefania, Papamoschou Vasilis, Raimo Monica, Mastrobattista Enrico, Caiazzo Massimiliano
Pharmaceutics Division, Faculty of Science, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.
Glycostem Therapeutics B.V., Kloosterstraat 9, 5349 AB Oss, The Netherlands.
Pharmaceutics. 2024 Aug 29;16(9):1143. doi: 10.3390/pharmaceutics16091143.
Natural killer (NK) cells have recently gained popularity as an alternative for cancer immunotherapy. Adoptive cell transfer employing NK cells offers a safer therapeutic option compared to T-cell-based therapies, due to their significantly lower toxicity and the availability of diverse autologous and allogeneic NK cell sources. However, several challenges are associated with NK cell therapies, including limited in vivo persistence, the immunosuppressive and hostile tumor microenvironment (TME), and the lack of effective treatments for solid tumors. To address these limitations, the modification of NK cells to stably produce cytokines has been proposed as a strategy to enhance their persistence and proliferation. Additionally, the overexpression of activating receptors and the blockade of inhibitory receptors can restore the NK cell functions hindered by the TME. To further improve tumor infiltration and the elimination of solid tumors, innovative approaches focusing on the enhancement of NK cell chemotaxis through the overexpression of chemotactic receptors have been introduced. This review highlights the latest advancements in preclinical and clinical studies investigating the engineering of activating, inhibitory, and chemotactic NK cell receptors; discusses recent progress in cytokine manipulation; and explores the potential of combining the chimeric antigen receptor (CAR) technology with NK cell receptors engineering.
自然杀伤(NK)细胞作为癌症免疫疗法的一种替代方案,近来颇受关注。与基于T细胞的疗法相比,采用NK细胞的过继性细胞转移提供了一种更安全的治疗选择,这是因为其毒性显著更低,且有多种自体和异体NK细胞来源可供使用。然而,NK细胞疗法存在若干挑战,包括体内持久性有限、免疫抑制性和恶劣的肿瘤微环境(TME),以及缺乏针对实体瘤的有效治疗方法。为解决这些局限性,有人提出对NK细胞进行改造,使其稳定产生细胞因子,作为增强其持久性和增殖能力的一种策略。此外,激活受体的过表达和抑制受体的阻断可恢复受TME阻碍的NK细胞功能。为进一步改善肿瘤浸润和实体瘤清除效果,已引入了一些创新方法,这些方法侧重于通过趋化受体的过表达来增强NK细胞的趋化性。本综述重点介绍了在研究激活型、抑制型和趋化型NK细胞受体工程的临床前和临床研究中的最新进展;讨论了细胞因子调控方面的最新进展;并探讨了将嵌合抗原受体(CAR)技术与NK细胞受体工程相结合的潜力。