Neuraminidase-Mediated, NKp46-Dependent Immune-Evasion Mechanism of Influenza Viruses

被引:46
作者
Bar-On, Yotam [1 ]
Glasner, Ariella [1 ]
Meningher, Tal [2 ,3 ]
Achdout, Hagit [1 ,4 ]
Gur, Chamutal [1 ]
Lankry, Dikla [1 ]
Vitenshtein, Alon [1 ]
Meyers, Adrienne F. A. [5 ,6 ]
Mandelboim, Michal [2 ]
Mandelboim, Ofer [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Fac Med, IMRIC,Lautenberg Ctr Gen & Tumor Immunol, IL-91120 Jerusalem, Israel
[2] Chaim Sheba Med Ctr, Publ Hlth Serv, Minist Hlth, Cent Virol Lab, IL-52662 Ramat Gan, Israel
[3] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, IL-52900 Ramat Gan, Israel
[4] Israel Inst Biol Res, Dept Infect Dis, IL-74100 Ness Ziona, Israel
[5] Publ Hlth Agcy Canada, Natl HIV & Retrovirol Labs, Natl Lab HIV Immunol, Winnipeg, MB R3E 3R2, Canada
[6] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB R3E 0J9, Canada
来源
CELL REPORTS | 2013年 / 3卷 / 04期
关键词
NATURAL-KILLER-CELLS; INFECTED CELLS; RECOGNITION; NKP46; HEMAGGLUTININS; INHIBITORS; TYPE-1; LYSIS;
D O I
10.1016/j.celrep.2013.03.034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1044 / 1050
页数:7
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