Combinatorial Regimens Augment Drug Monotherapy for SARS-CoV-2 Clearance in Mice.
Irfan UllahFanny EscudieIvan ScandaleZoela GilaniGabrielle Gendron-LepageFleur GaudetteCharles E MowbrayLaurent FraisseRenée BazinAndrés FinziWalther MothesPriti KumarEric ChatelainPradeep D UchilPublished in: bioRxiv : the preprint server for biology (2023)
Direct acting antivirals (DAAs) represent critical tools for combating SARS-CoV-2 variants of concern (VOCs) that evolve to escape spike-based immunity and future coronaviruses with pandemic potential. Here, we used bioluminescence imaging to evaluate therapeutic efficacy of DAAs that target SARS-CoV-2 RNA-dependent RNA polymerase (favipiravir, molnupiravir) or Main protease (nirmatrelvir) against Delta or Omicron VOCs in K18-hACE2 mice. Nirmatrelvir displayed the best efficacy followed by molnupiravir and favipiravir in suppressing viral loads in the lung. Unlike neutralizing antibody treatment, DAA monotherapy did not eliminate SARS-CoV-2 in mice. However, targeting two viral enzymes by combining molnupiravir with nirmatrelvir resulted in superior efficacy and virus clearance. Furthermore, combining molnupiravir with Caspase-1/4 inhibitor mitigated inflammation and lung pathology whereas combining molnupiravir with COVID-19 convalescent plasma yielded rapid virus clearance and 100% survival. Thus, our study provides insights into treatment efficacies of DAAs and other effective combinations to bolster COVID-19 therapeutic arsenal.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- combination therapy
- high fat diet induced
- oxidative stress
- coronavirus disease
- type diabetes
- cell death
- open label
- clinical trial
- signaling pathway
- emergency department
- randomized controlled trial
- copy number
- cancer therapy
- wild type
- replacement therapy
- endoplasmic reticulum stress