4.7 Article

Influenza polymerase inhibitor resistance: Assessment of the current state of the art-A report of the isirv Antiviral group

Journal

ANTIVIRAL RESEARCH
Volume 194, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.antiviral.2021.105158

Keywords

Influenza virus; Antiviral; Polymerase inhibitor; Baloxavir; Drug resistance; Fitness

Funding

  1. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services [HHSN272201400006C, 75N93021C00016]

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This article summarized the current knowledge on the clinical impact of resistance to polymerase inhibitors, surveillance methods, and laboratory evaluation methods. Limitations and gaps in current knowledge were highlighted, with suggestions for future research including additional clinical studies of influenza antiviral drug combinations. Lessons learned from influenza resistance monitoring may also be useful for establishing future drug susceptibility surveillance and testing for SARS-CoV-2.
It is more than 20 years since the neuraminidase inhibitors, oseltamivir and zanamivir were approved for the treatment and prevention of influenza. Guidelines for global surveillance and methods for evaluating resistance were established initially by the Neuraminidase Inhibitor Susceptibility Network (NISN), which merged 10 years ago with the International Society for influenza and other Respiratory Virus Diseases (isirv) to become the isirvAntiviral Group (isirv-AVG). With the ongoing development of new influenza polymerase inhibitors and recent approval of baloxavir marboxil, the isirv-AVG held a closed meeting in August 2019 to discuss the impact of resistance to these inhibitors. Following this meeting and review of the current literature, this article is intended to summarize current knowledge regarding the clinical impact of resistance to polymerase inhibitors and approaches for surveillance and methods for laboratory evaluation of resistance, both in vitro and in animal models. We highlight limitations and gaps in current knowledge and suggest some strategies for addressing these gaps, including the need for additional clinical studies of influenza antiviral drug combinations. Lessons learned from influenza resistance monitoring may also be helpful for establishing future drug susceptibility surveillance and testing for SARS-CoV-2.

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