Pulmonary vascular improvement in severe COVID-19 patients treated with tocilizumab.


Journal

Immunology letters
ISSN: 1879-0542
Titre abrégé: Immunol Lett
Pays: Netherlands
ID NLM: 7910006

Informations de publication

Date de publication:
12 2020
Historique:
received: 23 10 2020
accepted: 31 10 2020
pubmed: 9 11 2020
medline: 23 12 2020
entrez: 8 11 2020
Statut: ppublish

Résumé

As of October 2020 management of Coronavirus disease 2019 (COVID-19) is based on supportive care and off-label or compassionate-use therapies. On March 2020 tocilizumab - an anti-IL-6 receptor monoclonal antibody - was suggested as immunomodulatory treatment in severe COVID-19 because hyperinflammatory syndrome occurs in many patients similarly to the cytokine release syndrome that develops after CAR-T cell therapy. In our retrospective observational study, 20 severe COVID-19 patients requiring intensive care were treated with tocilizumab in addition to standard-of-care therapy (SOC) and compared with 13 COVID-19 patients receiving only SOC. Clinical respiratory status, inflammatory markers and vascular radiologic score improved after one week from tocilizumab administration. On the contrary, these parameters were stable or worsened in patients receiving only SOC. Despite major study limitations, improvement of alveolar-arterial oxygen gradient as well as vascular radiologic score after one week may account for improved pulmonary vascular perfusion and could explain the more rapid recovery of COVID-19 patients receiving tocilizumab compared to controls.

Identifiants

pubmed: 33161002
pii: S0165-2478(20)30405-3
doi: 10.1016/j.imlet.2020.10.009
pmc: PMC7644186
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Biomarkers 0
Receptors, Interleukin-6 0
tocilizumab I031V2H011

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

122-128

Informations de copyright

Copyright © 2020 European Federation of Immunological Societies. Published by Elsevier B.V. All rights reserved.

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Auteurs

Lorenzo Salvati (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Mariaelena Occhipinti (M)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Leonardo Gori (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Luca Ciani (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Alessio Mazzoni (A)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Laura Maggi (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Manuela Capone (M)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Paola Parronchi (P)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Immunology and Cell Therapy Unit, Careggi University Hospital, Florence, Italy.

Francesco Liotta (F)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Immunology and Cell Therapy Unit, Careggi University Hospital, Florence, Italy.

Vittorio Miele (V)

Department of Emergency Radiology, Careggi University Hospital, Florence, Italy.

Francesco Annunziato (F)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Flow Cytometry Diagnostic Center and Immunotherapy (CDCI), Careggi University Hospital, Florence, Italy.

Federico Lavorini (F)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Pneumology and Intensive Care Unit, Careggi University Hospital, Florence, Italy.

Lorenzo Cosmi (L)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Immunology and Cell Therapy Unit, Careggi University Hospital, Florence, Italy. Electronic address: lorenzo.cosmi@unifi.it.

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