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自然杀伤细胞免疫疗法治疗 B 细胞非霍奇金淋巴瘤(B 细胞 NHL)的未来。

The Future of Natural Killer Cell Immunotherapy for B Cell Non-Hodgkin Lymphoma (B Cell NHL).

机构信息

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.

出版信息

Curr Treat Options Oncol. 2022 Mar;23(3):381-403. doi: 10.1007/s11864-021-00932-2. Epub 2022 Mar 8.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72e0/8930876/243668f384a8/11864_2021_932_Fig1_HTML.jpg

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