TY - JOUR
T1 - Inhaled modified angiotensin converting enzyme 2 (ACE2) as a decoy to mitigate SARS-CoV-2 infection
AU - Ameratunga, Rohan
AU - Lehnert, Klaus
AU - Leung, Euphemia
AU - Comoletti, Davide
AU - Snell, Russell
AU - Woon, See Tarn
AU - Abbott, William
AU - Mears, Emily
AU - Steele, Richard
AU - McKee, Jeff
AU - Muscroff-Taylor, Andrew
AU - Ameratunga, Shanthi
AU - Medlicott, Natalie
AU - Das, Shyamal
AU - Rolleston, William
AU - Quinones-Mateu, Miguel E.
AU - Petousis-Harris, Helen
AU - Jordan, Anthony
N1 - Publisher Copyright:
© 2020 New Zealand Medical Association. All rights reserved.
PY - 2020/5/22
Y1 - 2020/5/22
N2 - 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.
AB - 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.
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M3 - Article
C2 - 32438383
AN - SCOPUS:85085155002
SN - 0028-8446
VL - 133
SP - 112
EP - 118
JO - New Zealand Medical Journal
JF - New Zealand Medical Journal
IS - 1515
ER -