Retrospective Multicenter Cohort Study Shows Early Interferon Therapy Is Associated with Favorable Clinical Responses in COVID-19 Patients.
Adolescent
Adult
Aged
Aged, 80 and over
Antiviral Agents
/ administration & dosage
Betacoronavirus
COVID-19
Child
China
/ epidemiology
Cohort Studies
Coronavirus Infections
/ drug therapy
Drug Therapy, Combination
Female
Hospital Mortality
Host Microbial Interactions
/ drug effects
Humans
Indoles
/ administration & dosage
Interferon alpha-2
Interferon-alpha
/ administration & dosage
Length of Stay
Lopinavir
/ administration & dosage
Male
Middle Aged
Pandemics
Pneumonia, Viral
/ drug therapy
Retrospective Studies
Ritonavir
/ administration & dosage
SARS-CoV-2
Treatment Outcome
Young Adult
COVID-19 Drug Treatment
RNA virus
anti-retroviral agents
anti-viral immunity
cytokine storm syndrome
infectious disease
respiratory medicine
viral infection
Journal
Cell host & microbe
ISSN: 1934-6069
Titre abrégé: Cell Host Microbe
Pays: United States
ID NLM: 101302316
Informations de publication
Date de publication:
09 09 2020
09 09 2020
Historique:
received:
09
06
2020
revised:
06
07
2020
accepted:
09
07
2020
pubmed:
25
7
2020
medline:
22
9
2020
entrez:
25
7
2020
Statut:
ppublish
Résumé
Interferons (IFNs) are widely used in treating coronavirus disease 2019 (COVID-19) patients. However, a recent report of ACE2, the host factor mediating SARS-Cov-2 infection, identifying it as interferon-stimulated raised considerable safety concern. To examine the association between the use and timing of IFN-α2b and clinical outcomes, we analyzed in a retrospective multicenter cohort study of 446 COVID-19 patients in Hubei, China. Regression models estimated that early administration (≤5 days after admission) of IFN-α2b was associated with reduced in-hospital mortality in comparison with no admission of IFN-α2b, whereas late administration of IFN-α2b was associated with increased mortality. Among survivors, early IFN-α2b was not associated with hospital discharge or computed tomography (CT) scan improvement, whereas late IFN-α2b was associated with delayed recovery. Additionally, early IFN-α2b and umifenovir alone or together were associated with reduced mortality and accelerated recovery in comparison with treatment with lopinavir/ritonavir (LPV/r) alone. We concluded that administration of IFN-α2b during the early stage of COVID-19 could induce favorable clinical responses.
Identifiants
pubmed: 32707096
pii: S1931-3128(20)30401-7
doi: 10.1016/j.chom.2020.07.005
pmc: PMC7368656
pii:
doi:
Substances chimiques
Antiviral Agents
0
Indoles
0
Interferon alpha-2
0
Interferon-alpha
0
Interferon-alpha2b
0
Lopinavir
2494G1JF75
umifenovir
93M09WW4RU
Ritonavir
O3J8G9O825
Types de publication
Journal Article
Multicenter Study
Observational Study
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
455-464.e2Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Interests The authors declare no competing interests.
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