Vaněk Ondřej, Kalousková Barbora, Abreu Celeste, Nejadebrahim Shiva, Skořepa Ondřej
Department of Biochemistry, Faculty of Science, Charles University, Prague, Czech Republic.
Department of Biochemistry, Faculty of Science, Charles University, Prague, Czech Republic.
Adv Protein Chem Struct Biol. 2022;129:91-133. doi: 10.1016/bs.apcsb.2022.02.001. Epub 2022 Mar 4.
Natural killer (NK) cells are a family of lymphocytes with a natural ability to kill infected, harmed, or malignantly transformed cells. As these cells are part of the innate immunity, the cytotoxic mechanisms are activated upon recognizing specific patterns without prior antigen sensitization. This recognition is crucial for NK cell function in the maintenance of homeostasis and immunosurveillance. NK cells not only act directly toward malignant cells but also participate in the complex immune response by producing cytokines or cross-talk with other immune cells. Cancer may be seen as a break of all immune defenses when malignant cells escape the immunity and invade surrounding tissues creating a microenvironment supporting tumor progression. This process may be reverted by intervening immune response with immunotherapy, which may restore immune recognition. NK cells are important effector cells for immunotherapy. They may be used for adoptive cell transfer, genetically modified with chimeric antigen receptors, or triggered with appropriate antibodies and other antibody-fragment-based recombinant therapeutic proteins tailored specifically for NK cell engagement. NK cell receptors, responsible for target recognition and activation of cytotoxic response, could also be targeted in immunotherapy, for example, by various bi-, tri-, or multi-specific fusion proteins designed to bridge the gap between tumor markers present on target cells and activation receptors expressed on NK cells. However, this kind of immunoactive therapeutics may be developed only with a deep functional and structural knowledge of NK cell receptor: ligand interactions. This review describes the recent developments in the fascinating protein-engineering field of NK cell immunotherapeutics.
自然杀伤(NK)细胞是一类淋巴细胞,具有天然杀伤被感染、受损或恶性转化细胞的能力。由于这些细胞是固有免疫的一部分,其细胞毒性机制在识别特定模式时被激活,无需事先进行抗原致敏。这种识别对于NK细胞在维持体内平衡和免疫监视中的功能至关重要。NK细胞不仅直接作用于恶性细胞,还通过产生细胞因子或与其他免疫细胞相互作用参与复杂的免疫反应。当恶性细胞逃避免疫并侵入周围组织,形成支持肿瘤进展的微环境时,癌症可被视为所有免疫防御的崩溃。通过免疫疗法干预免疫反应可能会逆转这一过程,免疫疗法可以恢复免疫识别。NK细胞是免疫疗法的重要效应细胞。它们可用于过继性细胞转移,用嵌合抗原受体进行基因改造,或用专门为NK细胞设计的合适抗体和其他基于抗体片段的重组治疗性蛋白触发。负责靶标识别和细胞毒性反应激活的NK细胞受体也可成为免疫疗法的靶点,例如,通过各种双特异性、三特异性或多特异性融合蛋白来弥合靶细胞上存在的肿瘤标志物与NK细胞上表达的激活受体之间的差距。然而,只有在深入了解NK细胞受体:配体相互作用的功能和结构知识的基础上,才能开发出这种免疫活性疗法。本综述描述了NK细胞免疫疗法这一引人入胜的蛋白质工程领域的最新进展。