Prophylactic Treatment with Baloxavir Protects Mice from Lethal Infection with Influenza A and B Viruses

Viruses. 2023 Nov 16;15(11):2264. doi: 10.3390/v15112264.

Abstract

Influenza remains a worldwide health concern. Antiviral drugs are considered as one of the useful options for its prevention as a complementary measure to vaccination. Baloxavir acid selectively inhibits the cap-dependent endonuclease of influenza viruses and exhibits marked viral titre reduction in patients. Here, we describe the prophylactic potency of baloxavir acid against lethal infection with influenza A and B viruses in mice. BALB/c mice were subcutaneously administered once with baloxavir acid suspension, or orally administered once daily for 10 days with oseltamivir phosphate solution at human relevant doses. Next, the mice were intranasally inoculated with A/PR/8/34 (H1N1) or B/Hong Kong/5/72 strain at 24 to 96 h after the initial dosing. Prophylactic treatment with the antiviral drugs significantly reduced the lung viral titres and prolonged survival time. In particular, baloxavir acid showed a greater suppressive effect on lung viral titres compared to oseltamivir phosphate. In this model, baloxavir acid maintained significant prophylactic effects against influenza A and B virus infections when the plasma concentration at the time of infection was at least 0.88 and 3.58 ng/mL, respectively. The significant prophylactic efficacy observed in our mouse model suggests the potential utility of baloxavir marboxil for prophylaxis against influenza in humans.

Keywords: baloxavir acid; baloxavir marboxil; cap-dependent endonuclease inhibitor; influenza virus; oseltamivir phosphate; prophylaxis.

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Herpesvirus 1, Cercopithecine*
  • Humans
  • Influenza A Virus, H1N1 Subtype*
  • Influenza, Human* / drug therapy
  • Influenza, Human* / prevention & control
  • Mice
  • Mice, Inbred BALB C
  • Oseltamivir / pharmacology
  • Oseltamivir / therapeutic use
  • Oxazines / therapeutic use
  • Phosphates
  • Pyridines / therapeutic use
  • Thiepins* / pharmacology
  • Thiepins* / therapeutic use

Substances

  • baloxavir
  • Oseltamivir
  • Oxazines
  • Pyridines
  • Thiepins
  • Antiviral Agents
  • Phosphates

Grants and funding

This study was sponsored by Shionogi and Co., Ltd., manufacturer/licensee of baloxavir marboxil. All authors are employees of Shionogi and Co., Ltd or Shionogi TechnoAdvance Research, Co., Ltd, an affiliation of Shionogi.