Baloxavir Marboxil Treatment of Nude Mice Infected With Influenza A Virus

Abstract Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses. Methods In this st...

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Published inThe Journal of infectious diseases Vol. 221; no. 10; pp. 1699 - 1702
Main Authors Kiso, Maki, Yamayoshi, Seiya, Murakami, Jurika, Kawaoka, Yoshihiro
Format Journal Article
LanguageEnglish
Published US Oxford University Press 27.04.2020
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Abstract Abstract Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses. Methods In this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient. Results Daily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment. Conclusions Despite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.
AbstractList Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses.BACKGROUNDImmunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses.In this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient.METHODSIn this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient.Daily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment.RESULTSDaily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment.Despite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.CONCLUSIONSDespite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.
Abstract Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses. Methods In this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient. Results Daily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment. Conclusions Despite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.
Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses. Methods In this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient. Results Daily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment. Conclusions Despite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.
Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to eradicate the virus from the respiratory tract, leading to the emergence of drug-resistant mutant viruses. In this study, we examined the efficacy of baloxavir marboxil in nude mice that were immunologically deficient. Daily treatment with a suboptimal dose of baloxavir marboxil increased the survival time of the virus-infected nude mice but did not clear the virus from their respiratory organs, resulting in gradual body weight loss after termination of treatment. Despite the prolonged baloxavir marboxil treatment, few resistant mutants were detected.
Author Yamayoshi, Seiya
Murakami, Jurika
Kawaoka, Yoshihiro
Kiso, Maki
AuthorAffiliation 2 Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison , Madison, Wisconsin, USA
3 Department of Special Pathogens, International Research Center for Infectious Diseases, Institute of Medical Science, University of Tokyo , Tokyo, Japan
1 Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan
AuthorAffiliation_xml – name: 2 Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison , Madison, Wisconsin, USA
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ContentType Journal Article
Copyright The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2019
The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
Copyright_xml – notice: The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2019
– notice: The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
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Keywords influenza
baloxavir marboxil
drug resistance
immunocompromised
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Snippet Abstract Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients...
Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not able to...
Background Immunocompromised patients infected with influenza virus require prolonged treatment with neuraminidase inhibitors, because these patients are not...
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SubjectTerms Animals
Antiviral Agents - administration & dosage
Antiviral Agents - therapeutic use
Antiviral drugs
Body weight
Body weight loss
Dibenzothiepins - administration & dosage
Dibenzothiepins - therapeutic use
Dose-Response Relationship, Drug
Drug resistance
Exo-a-sialidase
Immunocompromised hosts
Influenza
Influenza A
Influenza A virus
Major and Brief Reports
Male
Mice
Mice, Nude
Morpholines - administration & dosage
Morpholines - therapeutic use
Orthomyxoviridae Infections - drug therapy
Orthomyxoviridae Infections - veterinary
Orthomyxoviridae Infections - virology
Pyridones - administration & dosage
Pyridones - therapeutic use
Resistant mutant
Respiratory organs
Respiratory tract
Triazines - administration & dosage
Triazines - therapeutic use
Viruses
Title Baloxavir Marboxil Treatment of Nude Mice Infected With Influenza A Virus
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