4.7 Article

Detection of Variants With Reduced Baloxavir Marboxil and Oseltamivir Susceptibility in Children With Influenza A During the 2019-2020 Influenza Season

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 224, Issue 10, Pages 1735-1741

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab196

Keywords

influenza; baloxavir; oseltamivir; antiviral therapy; resistance; children; I38T; I38F; A37T; H275Y

Funding

  1. Ministry of Health, Labor and Welfare, Japan [10110400]
  2. Japan Society for the Promotion of Science (JSPS) KAKENHI [18K10036, 20K08210]
  3. Grants-in-Aid for Scientific Research [18K10036, 20K08210] Funding Source: KAKEN

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This study aimed to detect influenza variants with reduced susceptibility to baloxavir marboxil and oseltamivir, and to determine differences in clinical course in children with and without these variants post-antiviral treatment. The results showed that while the emergence of baloxavir-resistant variants may affect the clinical course of patients, oseltamivir-resistant variants had no clinical impact.
Background. We aimed to detect influenza variants with reduced susceptibility to baloxavir marboxil (baloxavir) and oseltamivir and identify differences in the clinical course between children with and without these variants after antiviral treatment. Methods. During the 2019-2020 influenza season, we enrolled children with confirmed influenza A (20 treated with baloxavir and 16 with oseltamivir). We analyzed patients' sequential viral RNA loads and infectious virus titers, the drug susceptibilities of clinical isolates, and amino acid substitutions in the viral polymerase acidic protein subunits or neuraminidase. We assessed patients' clinical information using questionnaires. Results. All viral RNA loads and virus titers were significantly decreased after treatment, but we detected baloxavir-resistant and oseltamivir-resistant variants in 5 of 20 and 3 of 16 patients, respectively. The duration of fever was similar between patients with and without the variants, but infectious viral shedding lasted 3 days longer in patients with baloxavir-resistant variants. In addition, the duration to improvement of clinical symptoms was longer in these patients (75.0 vs 29.5 hours; P. =.106). Conclusions. After antiviral treatment, the emergence of baloxavir-resistant variants may affect the patients' clinical course, but oseltamivir-resistant variants had no clinical impact.

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