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Azithromycin Plus Zinc Sulfate Rapidly and Synergistically Suppresses IκBα-Mediated In Vitro Human Airway Cell ACE2 Expression for SARS-CoV-2 Entry
Yin-Kai Chen; Tsung-Tao Huang; Chia-Wei Chang; Ming-Cheng Lee; Bor-Ru Lin; Yen-Pei Lu; Yih-Jen Hsu; Chun-Yu Chuang.
Affiliation
  • Yin-Kai Chen; National Taiwan University Cancer Center
  • Tsung-Tao Huang; Biomedical Platform and Incubation Services Division Taiwan Instrument Research Institute, National Applied Research Laboratories
  • Chia-Wei Chang; Biomedical Platform and Incubation Services Division Taiwan Instrument Research Institute, National Applied Research Laboratories
  • Ming-Cheng Lee; Department of Internal medicine, National Taiwan University Hospital
  • Bor-Ru Lin; Department of Integrated Diagnostics and Therapeutics, Department of Internal Medicine, National Taiwan Universtiy Hospital
  • Yen-Pei Lu; Biomedical Platform and Incubation Services Division Taiwan Instrument Research Institute, National Applied Research Laboratories
  • Yih-Jen Hsu; Department of Internal Medicine, National Taiwan University Hospital
  • Chun-Yu Chuang; Biomedical Engineering and Environmental Sciences, National Tsing Hua University
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-427206
ABSTRACT
Large-scale efforts have been persistently undertaken for medical prophylaxis and treatment of COVID-19 disasters worldwide. A variety of novel viral spike protein-targeted vaccine preparations have recently been clinically distributed based on accelerated approval. We revisited the early but inconclusive clinical interest in the combination of azithromycin and zinc sulfate repurposing with safety advantages. In vitro proof of concept was provided for rapid and synergistic suppression of ACE2 expression following treatments in human airway cells, Calu-3 and H322M. The two representative ACE2-expressing human airway cells indicate the upper and lower respiratory tracts. Prophylactic and early therapeutic roles of azithromycin combined with zinc are proposed for virus cellular entry prevention potential bridging to effective antibody production.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Prognostic_studies Language: En Year: 2021 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Prognostic_studies Language: En Year: 2021 Document type: Preprint