Université de Lille, CNRS, Inserm, CHU Lille, UMR9020-U1277 CANTHER, Lille, France.
These authors share first authorship.
Curr Protoc. 2024 Nov;4(11):e70040. doi: 10.1002/cpz1.70040.
Cellular immunotherapy has emerged as one of the most potent approaches to treating cancer patients. Adoptive transfer of chimeric antigen receptor (CAR) T cells as well as the use of haploidentical natural killer (NK) cells can induce remission in patients with lymphoma and leukemia. Although the use of CAR T cells has been established, this approach is currently limited for wider use by the risk of severe adverse events, including cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. Moreover, the risk of triggering graft vs host reactions in settings of allogeneic T cell infusion limits the use to autologous CAR T cells if advanced CRISPR engineering is not applied. In contrast, NK cell-based cancer immunotherapy has emerged as a safe approach even in allogeneic settings. However, efficient transduction of primary blood NK cells with vesicular stomatitis virus G glycoprotein (VSV-G) pseudotyped lentivirus commonly used for T cell modification remains challenging. This article presents a detailed method that significantly enhances the transduction efficiency of NK cells by utilizing a short-term culture in cytokine-supplemented medium. It also encompasses the preparation of high-titer and high-quality lentiviral particles for optimal NK cell transduction. Overall, this protocol details the step-by-step culture of NK cells in cytokine-supplemented medium, their transduction with VSV-G lentiviral vectors, and subsequent expansion for functional assays. © 2024 Wiley Periodicals LLC. Basic Protocol 1: Isolation of NK cells from human peripheral blood mononuclear cells (PBMCs) Basic Protocol 2: NK cell expansion and transduction with lentivirus for generating CAR-NK cells Support Protocol 1: Plasmid amplification Support Protocol 2: Lentivirus preparation Support Protocol 3: Lentivirus titration.
细胞免疫疗法已成为治疗癌症患者的最有效方法之一。嵌合抗原受体 (CAR) T 细胞的过继转移以及单倍体同种异体自然杀伤 (NK) 细胞的使用可以诱导淋巴瘤和白血病患者缓解。尽管 CAR T 细胞的使用已经确立,但由于包括细胞因子释放综合征和免疫效应细胞相关神经毒性综合征在内的严重不良事件的风险,该方法目前的使用受到限制。此外,如果不应用先进的 CRISPR 工程,同种异体 T 细胞输注情况下引发移植物抗宿主反应的风险限制了其在自体 CAR T 细胞中的使用。相比之下,NK 细胞为基础的癌症免疫疗法即使在同种异体环境中也已成为一种安全的方法。然而,利用常用于 T 细胞修饰的包膜糖蛋白 (VSV-G) 假型慢病毒有效转导原代血液 NK 细胞仍然具有挑战性。本文提出了一种详细的方法,通过利用在细胞因子补充培养基中的短期培养,可以显著提高 NK 细胞的转导效率。它还包括了高滴度和高质量慢病毒颗粒的制备,以实现最佳的 NK 细胞转导。总的来说,该方案详细描述了在细胞因子补充培养基中培养 NK 细胞、用 VSV-G 慢病毒载体转导 NK 细胞以及随后进行功能测定的扩展。© 2024 Wiley Periodicals LLC. 基本方案 1:从人外周血单核细胞 (PBMCs) 中分离 NK 细胞 基本方案 2:NK 细胞的扩增和慢病毒转导用于生成 CAR-NK 细胞 支持方案 1:质粒扩增 支持方案 2:慢病毒制备 支持方案 3:慢病毒滴定。