Type 3 hypersensitivity in COVID-19 vasculitis.


Journal

Clinical immunology (Orlando, Fla.)
ISSN: 1521-7035
Titre abrégé: Clin Immunol
Pays: United States
ID NLM: 100883537

Informations de publication

Date de publication:
08 2020
Historique:
received: 23 05 2020
revised: 26 05 2020
accepted: 27 05 2020
pubmed: 2 6 2020
medline: 22 7 2020
entrez: 2 6 2020
Statut: ppublish

Résumé

Coronavirus Disease 2019 (COVID-19) is an ongoing public health emergency and new knowledge about its immunopathogenic mechanisms is deemed necessary in the attempt to reduce the death burden, globally. For the first time in worldwide literature, we provide scientific evidence that in COVID-19 vasculitis a life-threatening escalation from type 2 T-helper immune response (humoral immunity) to type 3 hypersensitivity (immune complex disease) takes place. The subsequent deposition of immune complexes inside the vascular walls is supposed to induce a severe inflammatory state and a cytokine release syndrome, whose interleukin-6 is the key myokine, from the smooth muscle cells of blood vessels.

Identifiants

pubmed: 32479986
pii: S1521-6616(20)30452-6
doi: 10.1016/j.clim.2020.108487
pmc: PMC7256503
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Antigen-Antibody Complex 0
Complement C3 0
IL6 protein, human 0
Immunoglobulin G 0
Immunoglobulin M 0
Interleukin-6 0

Types de publication

Case Reports Letter

Langues

eng

Sous-ensembles de citation

IM

Pagination

108487

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None of the authors has any financial conflict of interest to disclose.

Références

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pubmed: 32360516
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pubmed: 17767747
Med Hypotheses. 2020 Sep;142:109824
pubmed: 32408068
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Clin Infect Dis. 2001 Jan;32(1):76-102
pubmed: 11118387
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pubmed: 16299724
Lancet. 2003 May 24;361(9371):1767-72
pubmed: 12781535
Arterioscler Thromb Vasc Biol. 2012 Jan;32(1):103-9
pubmed: 22034510
Br J Haematol. 2020 Jun;189(5):846-847
pubmed: 32304577

Auteurs

Luca Roncati (L)

Institute of Pathology, University of Modena and Reggio Emilia, Modena, Italy; Hemolymphopathology Team, University Hospital of Modena, Modena, Italy; Immunohistochemistry Lab, University Hospital of Modena, Modena, Italy. Electronic address: roncati.luca@aou.mo.it.

Giulia Ligabue (G)

Nephrology Lab, University of Modena and Reggio Emilia, Modena, Italy.

Luca Fabbiani (L)

Institute of Pathology, University of Modena and Reggio Emilia, Modena, Italy; Immunohistochemistry Lab, University Hospital of Modena, Modena, Italy.

Claudia Malagoli (C)

Institute of Pathology, University of Modena and Reggio Emilia, Modena, Italy; Immunohistochemistry Lab, University Hospital of Modena, Modena, Italy.

Graziana Gallo (G)

Institute of Pathology, University of Modena and Reggio Emilia, Modena, Italy.

Beatrice Lusenti (B)

Hemolymphopathology Team, University Hospital of Modena, Modena, Italy.

Vincenzo Nasillo (V)

Hemolymphopathology Team, University Hospital of Modena, Modena, Italy.

Antonio Manenti (A)

Department of Surgery, University of Modena and Reggio Emilia, Modena, Italy.

Antonio Maiorana (A)

Institute of Pathology, University of Modena and Reggio Emilia, Modena, Italy.

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Classifications MeSH