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Required concentration index quantifies effective drug combinations against hepatitis C virus infection.
Kakizoe, Yusuke; Koizumi, Yoshiki; Ikoma, Yukino; Ohashi, Hirofumi; Wakita, Takaji; Iwami, Shingo; Watashi, Koichi.
Afiliação
  • Kakizoe Y; Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka, 812-8581, Japan.
  • Koizumi Y; Present address: Data Science Group, Advanced Technology Division, INTAGE Inc, Tokyo, 101-8201, Japan.
  • Ikoma Y; National Center for Global Health and Medicine, Tokyo, 162-8655, Japan.
  • Ohashi H; Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka, 812-8581, Japan.
  • Wakita T; Department of Virology II, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
  • Iwami S; Department of Applied Biological Science, Tokyo University of Science, Noda, 278-8510, Japan.
  • Watashi K; Department of Virology II, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Theor Biol Med Model ; 18(1): 4, 2021 01 09.
Article em En | MEDLINE | ID: mdl-33422060
Successful clinical drug development requires rational design of combination treatments based on preclinical data. Anti-hepatitis C virus (HCV) drugs exhibit significant diversity in antiviral effect. Dose-response assessments can be used to determine parameters profiling the diverse antiviral effect during combination treatment. In the current study, a combined experimental and mathematical approaches were used to compare and score different combinations of anti-HCV treatments. A "required concentration index" was generated and used to rank the antiviral profile of possible double- and triple-drug combinations against HCV genotype 1b and 2a. Rankings varied based on target HCV genotype. Interestingly, multidrug (double and triple) treatment not only augmented antiviral activity, but also reduced genotype-specific efficacy, suggesting another advantage of multidrug treatment. The current study provides a quantitative method for profiling drug combinations against viral genotypes, to better inform clinical drug development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C / Hepacivirus Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Theor Biol Med Model Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C / Hepacivirus Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Theor Biol Med Model Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão