Department of Pediatrics, New York Medical College, Valhalla, NY, USA.
Hematology, Oncology, and Blood and Marrow Transplant Section, Nationwide Children's Hospital, Columbus, OH, USA.
Curr Treat Options Oncol. 2022 Mar;23(3):381-403. doi: 10.1007/s11864-021-00932-2. Epub 2022 Mar 8.
Natural killer (NK) cells have played a critical-if largely unrecognized or ignored-role in the treatment of B cell non-Hodgkin lymphoma (NHL) since the introduction of CD20-directed immunotherapy with rituximab as a cornerstone of therapy over 25 years ago. Engagement with NK cells leading to lysis of NHL targets through antibody-dependent cellular cytotoxicity (ADCC) is a critical component of rituximab's mechanism of action. Despite this important role, the only aspect of B cell NHL therapy that has been adopted as standard therapy that even indirectly augments or restores NK cell function is the introduction of obinutuzumab, a CD20 antibody with enhanced ability to engage with NK cells. However, over the last 5 years, adoptive immunotherapy with effector lymphocytes of B cell NHL has experienced tremendous growth, with five different CAR T cell products now licensed by the FDA, four of which target CD19 and have approved indications for some subtype of B cell NHL-axicabtagene ciloleucel, brexucabtagene autoleucel, lisocabtagene maraleucel, and tisagenlecleucel. These T cell-based immunotherapies essentially mimic the recognition, activation pathway, and cytotoxic machinery of a CD19 antibody engaging NK cells and lymphoma targets. Despite their efficacy, these T cell-based immunotherapies have been difficult to implement because they require 4-6 weeks of manufacture, are costly, and have significant toxicities. This renewed interest in the potential of cellular immunity-and the manufacturing, supply chain, and administration logistics that have been addressed with these new agents-have ignited a new wave of enthusiasm for NK cell-directed therapies in NHL. With high safety profiles and proven anti-lymphoma efficacy, one or more new NK cell-directed modalities are certain to be introduced into the standard toolbox of NHL therapy within the next few years, be it function-enhancing cytokine muteins, multi-domain NK cell engagers, or adoptive therapy with expanded or genetically modified NK cells.
自然杀伤 (NK) 细胞在 B 细胞非霍奇金淋巴瘤 (NHL) 的治疗中发挥了至关重要的作用——尽管在 25 年前引入利妥昔单抗作为治疗的基石,将 CD20 导向的免疫疗法作为 NHL 治疗的标准疗法以来,这种作用在很大程度上一直未被认识或忽视。通过抗体依赖性细胞毒性 (ADCC) 使 NK 细胞与 NHL 靶细胞结合并导致其裂解,是利妥昔单抗作用机制的关键组成部分。尽管 NK 细胞具有如此重要的作用,但唯一被采用为标准治疗方案、甚至间接增强或恢复 NK 细胞功能的 B 细胞 NHL 治疗方法是引入奥滨尤妥珠单抗,这是一种具有增强与 NK 细胞结合能力的 CD20 抗体。然而,在过去的 5 年中,B 细胞 NHL 的过继免疫疗法经历了巨大的发展,已有 5 种不同的 CAR T 细胞产品获得了 FDA 的批准,其中 4 种针对 CD19,并且针对某些 B 细胞 NHL 亚型有批准适应症——axicabtagene ciloleucel、brexucabtagene autoleucel、lisocabtagene maraleucel 和 tisagenlecleucel。这些基于 T 细胞的免疫疗法本质上模拟了识别、激活途径和与 NK 细胞和淋巴瘤靶细胞结合的 CD19 抗体的细胞毒性机制。尽管这些 T 细胞免疫疗法具有疗效,但由于它们需要 4-6 周的制造时间、成本高昂且具有显著的毒性,因此难以实施。对细胞免疫的潜在兴趣的重新关注——以及与这些新制剂相关的制造、供应链和管理后勤——激发了 NHL 中 NK 细胞定向治疗的新浪潮。由于具有较高的安全性和已被证实的抗淋巴瘤疗效,一种或多种新的 NK 细胞定向治疗方法肯定会在未来几年内被引入 NHL 治疗的标准工具包中,无论是增强功能的细胞因子突变体、多结构域 NK 细胞激动剂,还是用扩增或基因修饰的 NK 细胞进行过继治疗。