Granzin Markus, Wagner Juliane, Köhl Ulrike, Cerwenka Adelheid, Huppert Volker, Ullrich Evelyn
Clinical Research, Miltenyi Biotec Inc., Gaithersburg, MD, USA.
Division for Stem Cell Transplantation and Immunology, Department for Children and Adolescents Medicine, Hospital of the Goethe University, Frankfurt, Germany.
Front Immunol. 2017 Apr 26;8:458. doi: 10.3389/fimmu.2017.00458. eCollection 2017.
Natural killer (NK) cells are a promising tool for the use in adoptive immunotherapy, since they efficiently recognize and kill tumor cells. In this context, cultivation is an attractive option to increase NK cells in numbers and to improve their antitumor potential prior to clinical applications. Consequently, various strategies to generate NK cells for adoptive immunotherapy have been developed. Here, we give an overview of different NK cell cultivation approaches and their impact on shaping the NK cell antitumor activity. So far, the cytokines interleukin (IL)-2, IL-12, IL-15, IL-18, and IL-21 are used to culture and expand NK cells. The selection of the respective cytokine combination is an important factor that directly affects NK cell maturation, proliferation, survival, distribution of NK cell subpopulations, activation, and function in terms of cytokine production and cytotoxic potential. Importantly, cytokines can upregulate the expression of certain activating receptors on NK cells, thereby increasing their responsiveness against tumor cells that express the corresponding ligands. Apart from using cytokines, cocultivation with autologous accessory non-NK cells or addition of growth-inactivated feeder cells are approaches for NK cell cultivation with pronounced effects on NK cell activation and expansion. Furthermore, cultivation was reported to prime NK cells for the killing of tumor cells that were previously resistant to NK cell attack. In general, NK cells become frequently dysfunctional in cancer patients, for instance, by downregulation of NK cell activating receptors, disabling them in their antitumor response. In such scenario, cultivation can be helpful to arm NK cells with enhanced antitumor properties to overcome immunosuppression. In this review, we summarize the current knowledge on NK cell modulation by different cultivation strategies focused on increasing NK cytotoxicity for clinical application in malignant diseases. Moreover, we critically discuss the technical and regulatory aspects and challenges underlying NK cell based therapeutic approaches in the clinics.
自然杀伤(NK)细胞是过继性免疫疗法中一种很有前景的工具,因为它们能有效识别并杀死肿瘤细胞。在这种情况下,培养是一种有吸引力的选择,可在临床应用前增加NK细胞数量并提高其抗肿瘤潜力。因此,已开发出各种用于过继性免疫疗法的产生NK细胞的策略。在此,我们概述了不同的NK细胞培养方法及其对塑造NK细胞抗肿瘤活性的影响。到目前为止,细胞因子白细胞介素(IL)-2、IL-12、IL-15、IL-18和IL-21被用于培养和扩增NK细胞。选择各自的细胞因子组合是一个重要因素,它直接影响NK细胞的成熟、增殖、存活、NK细胞亚群的分布、激活以及在细胞因子产生和细胞毒性潜力方面的功能。重要的是,细胞因子可上调NK细胞上某些激活受体的表达,从而增强它们对表达相应配体的肿瘤细胞的反应性。除了使用细胞因子外,与自体辅助非NK细胞共培养或添加生长失活的饲养细胞也是NK细胞培养的方法,对NK细胞的激活和扩增有显著影响。此外,据报道培养可使NK细胞对先前抵抗NK细胞攻击的肿瘤细胞具有杀伤作用。一般来说,NK细胞在癌症患者中经常功能失调,例如,通过下调NK细胞激活受体,使其抗肿瘤反应失效。在这种情况下,培养有助于使NK细胞具备增强的抗肿瘤特性以克服免疫抑制。在本综述中,我们总结了关于不同培养策略对NK细胞调节的当前知识,重点是增强NK细胞毒性以用于恶性疾病的临床应用。此外,我们批判性地讨论了临床中基于NK细胞的治疗方法的技术、监管方面及挑战。