Weathering the Storm: Harnessing the Resolution of Inflammation to Limit COVID-19 Pathogenesis.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 27 01 2022
accepted: 22 03 2022
entrez: 26 5 2022
pubmed: 27 5 2022
medline: 28 5 2022
Statut: epublish

Résumé

The resolution of inflammation is a temporally and spatially coordinated process that in its innate manifestations, primarily involves neutrophils and macrophages. The shutdown of infection or injury-induced acute inflammation requires termination of neutrophil accumulation within the affected sites, neutrophil demise, and clearance by phagocytes (efferocytosis), such as tissue-resident and monocyte-derived macrophages. This must be followed by macrophage reprogramming from the inflammatory to reparative and consequently resolution-promoting phenotypes and the production of resolution-promoting lipid and protein mediators that limit responses in various cell types and promote tissue repair and return to homeostatic architecture and function. Recent studies suggest that these events, and macrophage reprogramming to pro-resolving phenotypes in particular, are not only important in the acute setting, but might be paramount in limiting chronic inflammation, autoimmunity, and various uncontrolled cytokine-driven pathologies. The SARS-CoV-2 (COVID-19) pandemic has caused a worldwide health and economic crisis. Severe COVID-19 cases that lead to high morbidity are tightly associated with an exuberant cytokine storm that seems to trigger shock-like pathologies, leading to vascular and multiorgan failures. In other cases, the cytokine storm can lead to diffuse alveolar damage that results in acute respiratory distress syndrome (ARDS) and lung failure. Here, we address recent advances on effectors in the resolution of inflammation and discuss how pro-resolution mechanisms with particular emphasis on macrophage reprogramming, might be harnessed to limit the universal COVID-19 health threat.

Identifiants

pubmed: 35615359
doi: 10.3389/fimmu.2022.863449
pmc: PMC9124752
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

863449

Subventions

Organisme : CIHR
ID : MOP-102619
Pays : Canada

Informations de copyright

Copyright © 2022 Silberberg, Filep and Ariel.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Esther Silberberg (E)

Department of Biology and Human Biology, University of Haifa, Haifa, Israel.

János G Filep (JG)

Department of Pathology and Cell Biology, University of Montreal, Montreal, QC, Canada.
Research Center, Maisonneuve-Rosemont Hospital, Montreal, QC, Canada.

Amiram Ariel (A)

Department of Biology and Human Biology, University of Haifa, Haifa, Israel.

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