Department of Pediatrics, Baylor College of Medicine, Center for Human Immunobiology, Texas Children's Hospital, Houston, TX, United States.
Front Immunol. 2018 Mar 7;9:445. doi: 10.3389/fimmu.2018.00445. eCollection 2018.
Human natural killer (NK) cells play a critical role in the control of viral infections and malignancy. Their importance in human health and disease is illustrated by severe viral infections in patients with primary immunodeficiencies that affect NK cell function and/or development. The recent identification of patients with phosphoinositide-3-kinase (PI3K)-signaling pathway mutations that can cause primary immunodeficiency provides valuable insight into the role that PI3K signaling plays in human NK cell maturation and lytic function. There is a rich literature that demonstrates a requirement for PI3K in multiple key aspects of NK cell biology, including development/maturation, homing, priming, and function. Here, I briefly review these previous studies and place them in context with recent findings from the study of primary immunodeficiency patients, particularly those with hyperactivating mutations in PI3Kδ signaling.
人类自然杀伤 (NK) 细胞在控制病毒感染和恶性肿瘤方面发挥着关键作用。NK 细胞在人类健康和疾病中的重要性体现在原发性免疫缺陷患者的严重病毒感染中,这些感染会影响 NK 细胞的功能和/或发育。最近发现的磷酸肌醇 3-激酶 (PI3K) 信号通路突变患者可导致原发性免疫缺陷,这为 PI3K 信号在人类 NK 细胞成熟和裂解功能中的作用提供了有价值的见解。有大量文献表明 PI3K 在 NK 细胞生物学的多个关键方面发挥作用,包括发育/成熟、归巢、激活和功能。在这里,我简要回顾了这些先前的研究,并将其置于与最近从原发性免疫缺陷患者研究中得出的发现的背景下,特别是那些具有 PI3Kδ 信号过度激活突变的患者。