Cellular Immunotherapy, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland.
Institute of Immunity & Transplantation, University College London Division of Infection & Immunity, London, UK.
Sci Rep. 2023 Jun 29;13(1):10555. doi: 10.1038/s41598-023-37779-6.
Human natural killer (NK) cells are cytotoxic effector cells that are increasingly harnessed in cancer immunotherapy. NKG2A/CD94 is an inhibitory receptor on NK cells that has established regulatory functions in the direct interaction with target cells when engaged with its ligand, the non-classical HLA class I molecule HLA-E. Here, we confirmed NKG2A as a checkpoint molecule in primary human NK cells and identified a novel role for NKG2A in maintaining NK cell expansion capacity by dampening both proliferative activity and excessive activation-induced cell death. Maintenance of NK cell expansion capacity might contribute to the preferential accumulation of human NKG2A NK cells after hematopoietic cell transplantation and enrichment of functionally impaired NK cells in human cancers. Functional silencing of NKG2A for cancer immunotherapy is highly attractive but will need to consider that this might also lead to a reduced survival by driving activation-induced cell death in targeted NK cells.
人类自然杀伤 (NK) 细胞是细胞毒性效应细胞,在癌症免疫治疗中越来越受到重视。NKG2A/CD94 是 NK 细胞上的抑制性受体,当与配体非经典 HLA I 类分子 HLA-E 结合时,在与靶细胞的直接相互作用中具有调节功能。在这里,我们证实了 NKG2A 是原代人 NK 细胞中的一个检查点分子,并确定了 NKG2A 通过抑制增殖活性和过度激活诱导的细胞死亡来维持 NK 细胞扩增能力的新作用。维持 NK 细胞扩增能力可能有助于在造血细胞移植后优先积累人 NKG2A NK 细胞,并在人类癌症中富集功能受损的 NK 细胞。针对癌症免疫治疗而对 NKG2A 进行功能沉默具有很大的吸引力,但需要考虑到这也可能通过在靶向 NK 细胞中驱动激活诱导的细胞死亡而导致存活率降低。