Immune responses in mildly versus critically ill COVID-19 patients.

COVID-19 SARS-CoV-2 T cells antibodies cytokine storm immune response inflammation therapeutic targets

Journal

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

Informations de publication

Date de publication:
2023
Historique:
received: 22 10 2022
accepted: 12 01 2023
entrez: 16 2 2023
pubmed: 17 2 2023
medline: 18 2 2023
Statut: epublish

Résumé

The current coronavirus pandemic (COVID-19), caused by SARS-CoV-2, has had devastating effects on the global health and economic system. The cellular and molecular mediators of both the innate and adaptive immune systems are critical in controlling SARS-CoV-2 infections. However, dysregulated inflammatory responses and imbalanced adaptive immunity may contribute to tissue destruction and pathogenesis of the disease. Important mechanisms in severe forms of COVID-19 include overproduction of inflammatory cytokines, impairment of type I IFN response, overactivation of neutrophils and macrophages, decreased frequencies of DC cells, NK cells and ILCs, complement activation, lymphopenia, Th1 and Treg hypoactivation, Th2 and Th17 hyperactivation, as well as decreased clonal diversity and dysregulated B lymphocyte function. Given the relationship between disease severity and an imbalanced immune system, scientists have been led to manipulate the immune system as a therapeutic approach. For example, anti-cytokine, cell, and IVIG therapies have received attention in the treatment of severe COVID-19. In this review, the role of immunity in the development and progression of COVID-19 is discussed, focusing on molecular and cellular aspects of the immune system in mild vs. severe forms of the disease. Moreover, some immune- based therapeutic approaches to COVID-19 are being investigated. Understanding key processes involved in the disease progression is critical in developing therapeutic agents and optimizing related strategies.

Identifiants

pubmed: 36793739
doi: 10.3389/fimmu.2023.1077236
pmc: PMC9923185
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

1077236

Informations de copyright

Copyright © 2023 Nasrollahi, Talepoor, Saleh, Eshkevar Vakili, Heydarinezhad, Karami, Noroozi, Meri and Kalantar.

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

Hamid Nasrollahi (H)

Radio-Oncology Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Atefe Ghamar Talepoor (AG)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Zahra Saleh (Z)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Mahsa Eshkevar Vakili (M)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Paria Heydarinezhad (P)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Narges Karami (N)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Maryam Noroozi (M)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Seppo Meri (S)

Department of Bacteriology and Immunology, University of Helsinki and Diagnostic Center of the Helsinki University Hospital, Helsinki, Finland.

Kurosh Kalantar (K)

Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Autoimmune Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

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