About: Host–Virus Interaction: How Host Cells Defend against Influenza A Virus Infection

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An Entity of Type : schema:ScholarlyArticle, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Host–Virus Interaction: How Host Cells Defend against Influenza A Virus Infection
Creator	Cao, Yongchang Zhang, Yun Xu, Zhichao
Source	PMC
abstract	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.
has issue date	2020-03-29(xsd:dateTime)
bibo:doi	10.3390/v12040376
bibo:pmid	32235330
has license	cc-by
sha1sum (hex)	d747e97f97ae31f6cf0a4f1bc1a6bc071cdc21b9
schema:url	https://doi.org/10.3390/v12040376
resource representing a document's title	Host–Virus Interaction: How Host Cells Defend against Influenza A Virus Infection
has PubMed Central identifier	PMC7232439
has PubMed identifier	32235330
schema:publication	Viruses
resource representing a document's body	covid:d747e97f97ae31f6cf0a4f1bc1a6bc071cdc21b9#body_text
is schema:about of	named entity 'highly' named entity 'triggered' named entity 'specific' named entity 'strategies' named entity 'Interaction' named entity 'CLEAR' named entity 'CASES' named entity 'ANTIVIRAL' named entity 'WORK' named entity 'NUMEROUS' named entity 'IAV' named entity 'viruses' named entity 'human' named entity 'innate immune system' named entity 'antagonize' named entity 'virus' named entity 'general' named entity 'current' named entity 'pathogens' named entity 'host cells' named entity 'global health' named entity 'adaptive immunity' named entity 'IAV' named entity 'nucleoprotein' named entity 'type I interferon' named entity 'caspase 9' named entity 'innate immunity' named entity 'protein kinase' named entity 'FAS' named entity 'AIV' named entity 'nucleotide analogue' named entity 'TGN' named entity 'viral infection' named entity 'apoptotic' named entity 'virion' named entity 'cellular metabolism' named entity 'Beclin-1' named entity 'viruses' named entity 'daisy-chain' named entity 'IFN' named entity 'ubiquitination' named entity 'polymerase' named entity 'viral titers' named entity 'RIG-I' named entity 'PARP1' named entity 'infection' named entity 'Alveolar type II epithelial cells' named entity 'polymerase' named entity 'Neutrophils' named entity 'neutrophils' named entity 'transcriptional' named entity 'H3N2' named entity 'protease' named entity 'MxA' named entity 'JAK-STAT' named entity 'antiviral' named entity 'secretion' named entity 'receptor binding domain' named entity 'autophagosome' named entity 'IAV' named entity 'transcriptome' named entity 'lower respiratory tract' named entity 'transmembrane' named entity 'reassortment' named entity 'CCR7' named entity 'infection' named entity 'DCs' named entity 'infection' named entity 'B lymphocytes' named entity 'mice' named entity 'virus' named entity 'IAV' named entity 'anti-inflammatory' named entity 'protein' named entity 'monomer' named entity 'macrophages' named entity 'goblet cells' named entity 'infection' named entity 'NF-κB'

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