Literature DB >> 27651415

Protease Inhibitor Resistance Remains Even After Mutant Strains Become Undetectable by Deep Sequencing.

Hiromi Kan1,2, Michio Imamura1,2, Takuro Uchida1,2, Nobuhiko Hiraga1,2, C Nelson Hayes1,2, Masataka Tsuge1,2, Hiromi Abe1,2, Hiroshi Aikata1,2, Grace Naswa Makokha1,2, Sajeda Chowdhury1,2, Daiki Miki2,3, Hidenori Ochi2,3, Yuji Ishida2,4, Chise Tateno2,4, Kazuaki Chayama1,2,3.   

Abstract

BACKGROUND: Although treatment-emergent NS3/4A protease inhibitor (PI)-resistant variants typically decrease in frequency after cessation of PI therapy in patients with chronic hepatitis C virus (HCV) infection, HCV susceptibility to PIs in patients who have not responded to previous PI therapy has not been addressed.
METHODS: Patients with chronic HCV genotype 1 infection were treated either with simeprevir plus interferon or with daclatasvir plus asunaprevir. Frequencies of drug-resistant mutations among patients with treatment failure were analyzed by deep sequencing. Human hepatocyte chimeric mice were injected with serum samples obtained from either treatment-naive patients or nonresponders to treatment with daclatasvir plus asunaprevir and then were treated with simeprevir and sofosbuvir.
RESULTS: Virological response to daclatasvir plus asunaprevir treatment was significantly lower in patients with simeprevir treatment failure as compared to those without previous treatment. Deep-sequencing analysis showed that the frequency of PI treatment-emergent NS3-D168 mutations gradually decreased and were completely replaced by wild-type genes after cessation of therapy. However, mice injected with serum obtained from a patient with PI treatment failure rapidly developed NS3-D168 mutations at significantly higher frequencies following either simeprevir or sofosbuvir treatment.
CONCLUSIONS: The virological response to daclatasvir plus asunaprevir treatment was low in patients with simeprevir treatment failure. PI resistance remains even after disappearance of mutant strains by deep sequencing.
© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail journals.permissions@oup.com.

Entities:  

Keywords:  NS3/4A protease inhibitor; NS5B polymerase inhibitor; chimeric mouse; direct-acting antiviral agent; drug resistance; hepatitis C virus

Mesh:

Substances:

Year:  2016        PMID: 27651415     DOI: 10.1093/infdis/jiw437

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  3 in total

1.  Synthesis and biological evaluation of tricyclic matrinic derivatives as a class of novel anti-HCV agents.

Authors:  Sheng Tang; Zong-Gen Peng; Ying-Hong Li; Xin Zhang; Tian-Yun Fan; Jian-Dong Jiang; Yan-Xiang Wang; Dan-Qing Song
Journal:  Chem Cent J       Date:  2017-09-29       Impact factor: 4.215

2.  HA1077 displays synergistic activity with daclatasvir against hepatitis C virus and suppresses the emergence of NS5A resistance-associated substitutions in mice.

Authors:  Seung-Hoon Lee; Jae-Su Moon; Bo-Yeong Pak; Geon-Woo Kim; Wooseong Lee; Hee Cho; SangKyu Kim; Seong-Jun Kim; Jong-Won Oh
Journal:  Sci Rep       Date:  2018-08-20       Impact factor: 4.379

3.  Drug repurposing of pyrimidine analogs as potent antiviral compounds against human enterovirus A71 infection with potential clinical applications.

Authors:  Jialei Sun; Thinesshwary Yogarajah; Regina Ching Hua Lee; Parveen Kaur; Masafumi Inoue; Yong Wah Tan; Justin Jang Hann Chu
Journal:  Sci Rep       Date:  2020-05-18       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.