Prophylactic efficacy of a human monoclonal antibody against MERS-CoV in the common marmoset.


Journal

Antiviral research
ISSN: 1872-9096
Titre abrégé: Antiviral Res
Pays: Netherlands
ID NLM: 8109699

Informations de publication

Date de publication:
03 2019
Historique:
received: 21 01 2019
accepted: 23 01 2019
pubmed: 27 1 2019
medline: 14 3 2020
entrez: 27 1 2019
Statut: ppublish

Résumé

Effective antiviral treatments for MERS-CoV are urgently needed. LCA60 is a MERS-CoV-neutralizing monoclonal antibody isolated from a convalescent MERS patient. Previously, it was shown that treatment with LCA60 resulted in reduced disease and virus titers in mouse models of MERS-CoV infection. Here, we tested the prophylactic efficacy of LCA60 in the common marmoset model of MERS-CoV infection. Intravenous administration of LCA60 one day before virus challenge resulted in high levels of MERS-CoV-neutralizing activity in circulating blood. Clinically, there was a moderate benefit of treatment with LCA60 including reduced respiratory involvement. Although viral lung loads were not reduced in LCA60-treated animals as compared to controls, there were fewer pathological changes in the lungs. Thus, prophylactic LCA60 treatment could be implemented to reduce disease burden in contacts of confirmed MERS-CoV patients.

Identifiants

pubmed: 30684561
pii: S0166-3542(19)30036-1
doi: 10.1016/j.antiviral.2019.01.016
pmc: PMC7113761
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Neutralizing 0
Antibodies, Viral 0

Types de publication

Journal Article Research Support, N.I.H., Intramural Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

70-74

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

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Auteurs

Emmie de Wit (E)

Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Friederike Feldmann (F)

Rocky Mountain Veterinary Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Eva Horne (E)

Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Atsushi Okumura (A)

Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY, USA.

Elisabetta Cameroni (E)

Humabs BioMed SA, A Subsidiary of Vir Biotechnology, 6500, Bellinzona, Switzerland.

Elaine Haddock (E)

Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Greg Saturday (G)

Rocky Mountain Veterinary Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Dana Scott (D)

Rocky Mountain Veterinary Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.

Robin Gopal (R)

National Infection Service, Public Health England (PHE), London, NW9 5EQ, United Kingdom.

Maria Zambon (M)

National Infection Service, Public Health England (PHE), London, NW9 5EQ, United Kingdom.

Davide Corti (D)

Humabs BioMed SA, A Subsidiary of Vir Biotechnology, 6500, Bellinzona, Switzerland.

Heinz Feldmann (H)

Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA. Electronic address: feldmannh@niaid.nih.gov.

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Classifications MeSH