Inhaled modified angiotensin converting enzyme 2 (ACE2) as a decoy to mitigate SARS-CoV-2 infection.


Journal

The New Zealand medical journal
ISSN: 1175-8716
Titre abrégé: N Z Med J
Pays: New Zealand
ID NLM: 0401067

Informations de publication

Date de publication:
22 05 2020
Historique:
entrez: 22 5 2020
pubmed: 22 5 2020
medline: 29 5 2020
Statut: epublish

Résumé

COVID-19 is a new zoonotic disease caused by the SARS-CoV-2 virus. Since its emergence in Wuhan City, China, the virus has rapidly spread across the globe causing calamitous health, economic and societal consequences. It causes disproportionately severe disease in the elderly and those with co-morbidities, such as hypertension and diabetes. There is currently no proven treatment for COVID-19 and a safe and effective vaccine is at least a year away. The virus gains access to the respiratory epithelium through cell surface angiotensin converting enzyme 2 (ACE2). The receptor binding domain (RBD) of the virus is unlikely to mutate without loss of pathogenicity and thus represents an attractive target for antiviral treatment. Inhaled modified recombinant human ACE2, may bind SARS-CoV-2 and mitigate lung damage. This decoy strategy is unlikely to provoke an adverse immune response and may reduce morbidity and mortality in high-risk groups.

Identifiants

pubmed: 32438383

Substances chimiques

Recombinant Proteins 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0
Peptidyl-Dipeptidase A EC 3.4.15.1
ACE2 protein, human EC 3.4.17.23
Angiotensin-Converting Enzyme 2 EC 3.4.17.23

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112-118

Déclaration de conflit d'intérêts

Dr Rolleston reports affiliation with South Pacific Sera Ltd outside the submitted work; and is the Chair of the Life Sciences Network. Dr Petousis-Harris reports grants from GSK outside the submitted work.

Auteurs

Rohan Ameratunga (R)

Department of Clinical Immunology, Auckland Hospital, Auckland; Department of Virology and Immunology, Auckland Hospital, Auckland; Department of Molecular Medicine and Pathology, School of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland.

Klaus Lehnert (K)

School of Biological Sciences, University of Auckland, Auckland.

Euphemia Leung (E)

Auckland Cancer Society Research Centre, School of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland.

Davide Comoletti (D)

School of Biological Sciences, Victoria University of Wellington, Kelburn Parade, Wellington.

Russell Snell (R)

School of Biological Sciences, University of Auckland, Auckland.

See-Tarn Woon (ST)

Department of Virology and Immunology, Auckland Hospital, Auckland.

William Abbott (W)

Department of Surgery, Auckland Hospital, Auckland.

Emily Mears (E)

School of Biological Sciences, University of Auckland, Auckland.

Richard Steele (R)

Department of Virology and Immunology, Auckland Hospital, Auckland; Department of Respiratory Medicine, Wellington Hospital, Wellington.

Jeff McKee (J)

Ecosure-Avisure Group, Burleigh Heads, Queensland, Australia.

Andrew Muscroft-Taylor (A)

Callaghan Innovations, Protein Science and Engineering, Christchurch.

Shanthi Ameratunga (S)

Population Health Directorate, Counties Manukau District Health Board, Auckland.

Natalie Medlicott (N)

School of Pharmacy, University of Otago, Dunedin.

Shyamal Das (S)

School of Pharmacy, University of Otago, Dunedin.

William Rolleston (W)

South Pacific Sera, Timaru.

Miguel Quiñones-Mateu (M)

Department of Microbiology and Immunology, University of Otago, Dunedin.

Helen Petousis-Harris (H)

Faculty of Medical and Health Sciences, University of Auckland, Auckland.

Anthony Jordan (A)

Department of Clinical Immunology, Auckland Hospital, Auckland.

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Classifications MeSH