From infection to repair: Understanding the workings of our innate immune cells.

immunology innate immune cells sterile injury

Journal

WIREs mechanisms of disease
ISSN: 2692-9368
Titre abrégé: WIREs Mech Dis
Pays: United States
ID NLM: 9918227353306676

Informations de publication

Date de publication:
09 2022
Historique:
revised: 13 04 2022
received: 12 01 2022
accepted: 04 05 2022
pubmed: 9 6 2022
medline: 17 9 2022
entrez: 8 6 2022
Statut: ppublish

Résumé

In a world filled with microbes, some posing a threat to our body, our immune system is key to living a healthy life. The innate immune system is made of various cell types that act to guard our bodies. Unlike the adaptive immune system that has a specific response, our innate immune system encompasses cells that elicit unspecific immune responses, triggered whenever the right signals are detected. Our understanding of immunity started with the concept of our immune system only responding to "nonself" like the pathogens that invade our body. However, over the past few decades, we have learned that the immune system is more than an on/off switch that recognizes nonself. The innate immune system regularly patrols our bodies for pathogens and tissue damage. Our innate immune system not only seeks to resolve infection but also repair tissue injury, through phagocytosing debris and initiating the release of growth factors. Recently, we are starting to see that it is not just recognizing danger, our innate immune system plays a crucial role in repair. Innate immune cells phenotypically change during repair. In the context of severe injury or trauma, our innate immune system is modified quite drastically to help repair, resulting in reduced infection control. Moreover, these changes in immune cell function can be modified by sex as a biological variable. From past to present, in this overview, we provide a summary of the innate immune cells and pathways in infection and tissue repair. This article is categorized under: Immune System Diseases > Molecular and Cellular Physiology.

Identifiants

pubmed: 35674186
doi: 10.1002/wsbm.1567
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1567

Subventions

Organisme : CIHR
Pays : Canada

Informations de copyright

© 2022 Wiley Periodicals LLC.

Auteurs

Martin Mawhinney (M)

Department of Pharmacology and Therapeutics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.

Amelia Kulle (A)

Department of Pharmacology and Therapeutics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.

Ajitha Thanabalasuriar (A)

Department of Pharmacology and Therapeutics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
Department of Microbiology and Immunology, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.

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Classifications MeSH