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Microorganisms . Regulation of Host Immune Responses against Influenza A Virus Infection by Mitogen-Activated Protein Kinases (MAPKs)

tetano

Editor, Senior Moderator
Microorganisms


. 2020 Jul 17;8(7):E1067.
doi: 10.3390/microorganisms8071067.
Regulation of Host Immune Responses against Influenza A Virus Infection by Mitogen-Activated Protein Kinases (MAPKs)


Jiabo Yu[SUP] 1 [/SUP], Xiang Sun[SUP] 1 [/SUP], Jian Yi Gerald Goie[SUP] 2 3 [/SUP], Yongliang Zhang[SUP] 2 3 [/SUP]



Affiliations

Abstract

Influenza is a major respiratory viral disease caused by infections from the influenza A virus (IAV) that persists across various seasonal outbreaks globally each year. Host immune response is a key factor determining disease severity of influenza infection, presenting an attractive target for the development of novel therapies for treatments. Among the multiple signal transduction pathways regulating the host immune activation and function in response to IAV infections, the mitogen-activated protein kinase (MAPK) pathways are important signalling axes, downstream of various pattern recognition receptors (PRRs), activated by IAVs that regulate various cellular processes in immune cells of both innate and adaptive immunity. Moreover, aberrant MAPK activation underpins overexuberant production of inflammatory mediators, promoting the development of the "cytokine storm", a characteristic of severe respiratory viral diseases. Therefore, elucidation of the regulatory roles of MAPK in immune responses against IAVs is not only essential for understanding the pathogenesis of severe influenza, but also critical for developing MAPK-dependent therapies for treatment of respiratory viral diseases. In this review, we will summarise the current understanding of MAPK functions in both innate and adaptive immune response against IAVs and discuss their contributions towards the cytokine storm caused by highly pathogenic influenza viruses.

Keywords: MAPK; adaptive immunity; cytokine storm; inflammatory cytokines; influenza; innate immunity; pattern recognition receptors; respiratory viral diseases.
 
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