Combination Therapy Using Inhalable GapmeR and Recombinant ACE2 for COVID-19

Navin Kumar Verma*, Mobashar Hussain Urf Turabe Fazil, Shane P. Duggan, Dermot Kelleher

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Here we report our perspective on applying GapmeR technology in combination with recombinant angiotensin-converting enzyme 2 (ACE2) in the treatment of COVID-19 patients. GapmeR is a cell-permeating antisense single-stranded DNA molecule that can be designed to specifically target intracellular severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Once internalized into host cells, such as lung alveolar cells, GapmeR molecules can bind to the viral RNA. This RNA/DNA hybrid will then be degraded by the RNase H enzyme abundantly present in the host cells. GapmeRs can be delivered to COVID-19 patients through inhalation or via nebulization. SARS-CoV-2-targeted GapmeR can also be given to frontline healthcare workers as a prophylactic protection. The recombinant ACE2 protein, the efficacy of which is being evaluated in clinical trials, will bind to the spike (S) glycoprotein of extracellular SARS-CoV-2 and potentially block viral infectivity. We propose that combining inhalable SARS-CoV-2-targeted GapmeRs with recombinant ACE2 could provide a viable and rapidly implementable more effective therapeutic approach for eradicating SARS-CoV-2 and save millions of lives.

Original languageEnglish
Article number197
JournalFrontiers in Molecular Biosciences
Volume7
DOIs
Publication statusPublished - Aug 7 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© Copyright © 2020 Verma, Fazil, Duggan and Kelleher.

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology
  • Biochemistry, Genetics and Molecular Biology (miscellaneous)

Keywords

  • angiotensin-converting enzyme 2
  • COVID-19 (2019-nCoV)
  • GapmeR
  • nasal delivery
  • therapy

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