Host-Virus Interaction: How Host Cells Defend against Influenza A Virus Infection

被引:17
作者
Zhang, Yun [1 ]
Xu, Zhichao [1 ]
Cao, Yongchang [1 ]
机构
[1] Sun Yat Sen Univ, State Key Lab Biocontrol, Sch Life Sci, Guangzhou 510006, Peoples R China
来源
VIRUSES-BASEL | 2020年 / 12卷 / 04期
关键词
influenza A virus; innate immunity; adaptive immunity; RECEPTOR-BINDING SPECIFICITY; ADAPTIVE IMMUNE-RESPONSES; AVIAN INFLUENZA; ANTIVIRAL RESPONSES; NUCLEAR EXPORT; MITOCHONDRIAL PROTEIN; VIRAL NUCLEOPROTEIN; FAVIPIRAVIR T-705; RESPIRATORY-TRACT; MATRIX PROTEIN-2;
D O I
10.3390/v12040376
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza A viruses (IAVs) are highly contagious pathogens infecting human and numerous animals. The viruses cause millions of infection cases and thousands of deaths every year, thus making IAVs a continual threat to global health. Upon IAV infection, host innate immune system is triggered and activated to restrict virus replication and clear pathogens. Subsequently, host adaptive immunity is involved in specific virus clearance. On the other hand, to achieve a successful infection, IAVs also apply multiple strategies to avoid be detected and eliminated by the host immunity. In the current review, we present a general description on recent work regarding different host cells and molecules facilitating antiviral defenses against IAV infection and how IAVs antagonize host immune responses.
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页数:23
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共 234 条
[1]   Antiviral response elicited against avian influenza virus infection following activation of toll-like receptor (TLR)7 signaling pathway is attributable to interleukin (IL)-1β production [J].
Abdul-Cader M.S. ;
De Silva Senapathi U. ;
Nagy E. ;
Sharif S. ;
Abdul-Careem M.F. .
BMC Research Notes, 11 (1)
[2]   Critical Role of Natural Killer Cells in Lung Immunopathology During Influenza Infection in Mice [J].
Abdul-Careem, Mohamed F. ;
Mian, M. Firoz ;
Yue, Geoffry ;
Gillgrass, Amy ;
Chenoweth, Meghan J. ;
Barra, Nicole G. ;
Chew, Marianne V. ;
Chan, Tiffany ;
Al-Garawi, Amal A. ;
Jordana, Manel ;
Ashkar, Ali A. .
JOURNAL OF INFECTIOUS DISEASES, 2012, 206 (02) :167-177
[3]   Influenza neuraminidase [J].
Air, Gillian M. .
INFLUENZA AND OTHER RESPIRATORY VIRUSES, 2012, 6 (04) :245-256
[4]   Crystal structure of the M1 protein-binding domain of the influenza A virus nuclear export protein (NEP/NS2) [J].
Akarsu, H ;
Burmeister, WP ;
Petosa, C ;
Petit, I ;
Müller, CW ;
Ruigrok, RWH ;
Baudin, F .
EMBO JOURNAL, 2003, 22 (18) :4646-4655
[5]   Pulmonary immunity to viruses [J].
Allie, S. Rameeza ;
Randall, Troy D. .
CLINICAL SCIENCE, 2017, 131 (14) :1737-1762
[6]   Imbalanced pro- and anti-Th17 responses (IL-17/granulocyte colony-stimulating factor) predict fatal outcome in 2009 pandemic influenza [J].
Almansa, Raquel ;
Socias, Lorenzo ;
Ramirez, Paula ;
Martin-Loeches, Ignacio ;
Valles, Jordi ;
Loza, Ana ;
Rello, Jordi ;
Kelvin, David J. ;
Leon, Cristobal ;
Blanco, Jesus ;
Andaluz, David ;
Micheloud, Dariela ;
Maravi, Enrique ;
Ortiz de Lejarazu, Raul ;
Bermejo-Martin, Jesus F. .
CRITICAL CARE, 2011, 15 (05)
[7]   REGULATION OF THE EXTENT OF SPLICING OF INFLUENZA-VIRUS NS1 MESSENGER-RNA - ROLE OF THE RATES OF SPLICING AND OF THE NUCLEOCYTOPLASMIC TRANSPORT OF NS1 MESSENGER-RNA [J].
ALONSOCAPLEN, FV ;
KRUG, RM .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :1092-1098
[8]   A Rab11-and Microtubule-Dependent Mechanism for Cytoplasmic Transport of Influenza A Virus Viral RNA [J].
Amorim, Maria Joao ;
Bruce, Emily A. ;
Read, Eliot K. C. ;
Foeglein, Agnes ;
Mahen, Robert ;
Stuart, Amanda D. ;
Digard, Paul .
JOURNAL OF VIROLOGY, 2011, 85 (09) :4143-4156
[9]   Influenza A virus-induced apoptosis and virus propagation [J].
Ampomah, Patrick B. ;
Lim, Lina H. K. .
APOPTOSIS, 2020, 25 (1-2) :1-11
[10]   Formyl peptide receptor 2 is regulated by RNA mimics and viruses through an IFN-β-STAT3-dependent pathway [J].
Ampomah, Patrick B. ;
Moraes, Leonardo A. ;
Lukman, Hakim M. ;
Lim, Lina H. K. .
FASEB JOURNAL, 2018, 32 (03) :1468-1478