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Efficacy of late-onset antiviral treatment in immune-compromised hosts with persistent SARS-CoV-2 infection.

Carolin M LieberHae-Ji KangElizabeth B SobolikZachary M SticherVu L NgoAndrew T GewirtzAlexander A KolykhalovMichael G NatchusAlexander L GreningerMehul S SutharRichard K Plemper
Published in: bioRxiv : the preprint server for biology (2024)
T cell-depleted immunocompromised mouse model of SARS-CoV-2 infection, we explored therapeutic options of persistent infections with standard-of-care paxlovid, molnupiravir, and the experimental therapeutic 4'-FlU. Late-onset treatment initiated 14 days after infection was efficacious, but only 4'-FlU was rapidly sterilizing. No treatment-experienced viral variants with reduced susceptibility to the drugs emerged, albeit virus replication rebounded in animals of the paxlovid group after treatment end. This study supports the use of direct-acting antivirals for late-onset management of persistent SARS-CoV-2 infection in immunocompromised hosts. However, treatment courses likely require to be extended for maximal therapeutic benefit, calling for appropriately powered clinical trials to meet the specific needs of this patient group.
Keyphrases
  • late onset
  • early onset
  • clinical trial
  • mouse model
  • healthcare
  • randomized controlled trial
  • gene expression
  • combination therapy
  • smoking cessation
  • pain management
  • replacement therapy