The Lautenberg Center for General and Tumor Immunology, Institute for Medical Research Israel-Canada (IMRIC), Faculty of Medicine, Hebrew University Hadassah Medical School, Jerusalem 91120, Israel.
Central Virology Laboratory, Ministry of Health, Public Health Services, Chaim Sheba Medical Center, Tel Hashomer, Ramat-Gan 52662, Israel.
Cell Rep. 2013 Apr 25;3(4):1044-50. doi: 10.1016/j.celrep.2013.03.034. Epub 2013 Apr 18.
Natural killer (NK) cells play an essential role in the defense against influenza virus, one of the deadliest respiratory viruses known today. The NKp46 receptor, expressed by NK cells, is critical for controlling influenza infections, as influenza-virus-infected cells are eliminated through the recognition of the viral hemagglutinin (HA) protein by NKp46. Here, we describe an immune-evasion mechanism of influenza viruses that is mediated by the neuraminidase (NA) protein. By using various NA blockers, we show that NA removes sialic acid residues from NKp46 and that this leads to reduced recognition of HA. Furthermore, we provide in vivo and in vitro evidence for the existence of this NA-mediated, NKp46-dependent immune-evasion mechanism and demonstrate that NA inhibitors, which are commonly used for the treatment of influenza infections, are useful not only as blockers of virus budding but also as boosters of NKp46 recognition.
自然杀伤 (NK) 细胞在抵御流感病毒方面发挥着重要作用,流感病毒是当今已知最致命的呼吸道病毒之一。NK 细胞表达的 NKp46 受体对于控制流感感染至关重要,因为通过 NKp46 识别病毒血凝素 (HA) 蛋白可以消除流感病毒感染的细胞。在这里,我们描述了流感病毒的一种免疫逃逸机制,该机制由神经氨酸酶 (NA) 蛋白介导。通过使用各种 NA 阻断剂,我们表明 NA 从 NKp46 上除去唾液酸残基,从而导致 HA 的识别减少。此外,我们提供了体内和体外证据,证明了这种 NA 介导的、依赖 NKp46 的免疫逃逸机制的存在,并表明神经氨酸酶抑制剂,常用于治疗流感感染,不仅可作为阻止病毒出芽的抑制剂,还可作为增强 NKp46 识别的增效剂。