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 in | The Journal of infectious diseases Vol. 221; no. 10; pp. 1699 - 1702 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Oxford University Press
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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. |
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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 – name: 1 Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan – name: 3 Department of Special Pathogens, International Research Center for Infectious Diseases, Institute of Medical Science, University of Tokyo , Tokyo, Japan |
Author_xml | – sequence: 1 givenname: Maki surname: Kiso fullname: Kiso, Maki organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan – sequence: 2 givenname: Seiya orcidid: 0000-0001-7768-5157 surname: Yamayoshi fullname: Yamayoshi, Seiya organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan – sequence: 3 givenname: Jurika surname: Murakami fullname: Murakami, Jurika organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan – sequence: 4 givenname: Yoshihiro surname: Kawaoka fullname: Kawaoka, Yoshihiro email: yamayo@ims.u-tokyo.ac.jp organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan |
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CitedBy_id | crossref_primary_10_1371_journal_ppat_1011342 crossref_primary_10_1016_j_antiviral_2024_105961 crossref_primary_10_1101_cshperspect_a038687 crossref_primary_10_1002_2211_5463_13416 crossref_primary_10_1093_ve_veae027 crossref_primary_10_1016_j_jep_2022_116070 crossref_primary_10_1093_jac_dkaa393 crossref_primary_10_2147_DHPS_S470868 crossref_primary_10_3390_cryst12040550 crossref_primary_10_1016_j_antiviral_2021_105158 crossref_primary_10_3390_microorganisms8121968 |
Cites_doi | 10.1056/NEJMc1003749 10.1093/jac/dky462 10.1093/infdis/jix606 10.1038/s41598-018-27890-4 10.1056/NEJMoa1716197 10.2807/1560-7917.ES.2019.24.12.1900170 10.1086/598684 10.1371/journal.pone.0217307 10.1016/j.virusres.2011.03.022 10.3201/eid1704.101429 10.1086/500464 |
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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. |
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Keywords | influenza baloxavir marboxil drug resistance immunocompromised |
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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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