Loading…

Antivirals against HCV infection: the story thus far

Remarkable scientific breakthroughs have been made in the stride towards the development of potent and tolerable hepatitis C regimens within the last three decades. Earlier approaches involved the use of pegylated interferon alfa and ribavirin as standard-of-care treatment. Treating genotype 1a infe...

Full description

Saved in:
Bibliographic Details
Published in:Journal of infection in developing countries 2022-02, Vol.16 (2), p.231-243
Main Authors: Irekeola, Ahmad Adebayo, Ear, Engku Nur Syafirah, Mohd Amin, Nur Amalin Zahirah, Mustaffa, Nazri, Shueb, Rafidah Hanim
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c315t-9978f98fb62faf8ac1b71c09c392eebd5ada6b88f8515520c8bb5f26bae183533
cites
container_end_page 243
container_issue 2
container_start_page 231
container_title Journal of infection in developing countries
container_volume 16
creator Irekeola, Ahmad Adebayo
Ear, Engku Nur Syafirah
Mohd Amin, Nur Amalin Zahirah
Mustaffa, Nazri
Shueb, Rafidah Hanim
description Remarkable scientific breakthroughs have been made in the stride towards the development of potent and tolerable hepatitis C regimens within the last three decades. Earlier approaches involved the use of pegylated interferon alfa and ribavirin as standard-of-care treatment. Treating genotype 1a infection with this regimen which was at that time considered the gold standard for hepatitis C virus therapy was rife with challenges; safety and toxicity issues necessitated a rigorous quest for alternative regimens. Deeper understanding of the pathogenesis of hepatitis C virus ushered in the era of direct acting antiviral agents. These agents have been the subject of intensive research in the last two decades, leading to the development of drug classes such as protease inhibitors (e.g., grazoprevir), NS5A inhibitors (e.g., daclatasvir) and NS5B inhibitors (e.g., sofosbuvir). While many are still under development, several have been approved for hepatitis C therapy. A number of studies investigating the combination of direct acting antiviral agents with or without pegylated interferon and/or ribavirin for the treatment of chronic hepatitis have demonstrated sustained virologic response of > 90%. Given the array of direct acting antiviral agents currently available, the present landscape of hepatitis C therapy is now characterized by a gradual transition to all-oral interferon-free regimens. Despite these milestones, the WHO global target of eliminating hepatitis C as a public health problem by 2030 seems uncertain. In this review, we provide a concise account of the evolution and advancements in the development of anti-HCV regimens.
doi_str_mv 10.3855/jidc.14485
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2641001470</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2641001470</sourcerecordid><originalsourceid>FETCH-LOGICAL-c315t-9978f98fb62faf8ac1b71c09c392eebd5ada6b88f8515520c8bb5f26bae183533</originalsourceid><addsrcrecordid>eNpdkMFKAzEURYMotlY3foAMuBFhal4ymUnclaJWKLhRtyHJJJrSztQkI_Tvndoq4urdxbmXx0HoHPCYcsZuFr42YygKzg7QEERFclJyfPgnD9BJjAuMmaAMjtGAMiJ4AeUQFZMm-U8f1DJm6k35JqZsNn3NfOOsSb5tbrP0brOY2rDpUxczp8IpOnJ9wZ7t7wi93N89T2f5_OnhcTqZ54YCS7kQFXeCO10SpxxXBnQFBgtDBbFW10zVqtScO86AMYIN15o5UmplgVNG6Qhd7XbXof3obExy5aOxy6VqbNtFScoCMIaiwj16-Q9dtF1o-u8kBQpVVQq8pa53lAltjME6uQ5-pcJGApZbl3LrUn677OGL_WSnV7b-RX_k0S9kjm3A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3131776900</pqid></control><display><type>article</type><title>Antivirals against HCV infection: the story thus far</title><source>Publicly Available Content Database</source><creator>Irekeola, Ahmad Adebayo ; Ear, Engku Nur Syafirah ; Mohd Amin, Nur Amalin Zahirah ; Mustaffa, Nazri ; Shueb, Rafidah Hanim</creator><creatorcontrib>Irekeola, Ahmad Adebayo ; Ear, Engku Nur Syafirah ; Mohd Amin, Nur Amalin Zahirah ; Mustaffa, Nazri ; Shueb, Rafidah Hanim</creatorcontrib><description>Remarkable scientific breakthroughs have been made in the stride towards the development of potent and tolerable hepatitis C regimens within the last three decades. Earlier approaches involved the use of pegylated interferon alfa and ribavirin as standard-of-care treatment. Treating genotype 1a infection with this regimen which was at that time considered the gold standard for hepatitis C virus therapy was rife with challenges; safety and toxicity issues necessitated a rigorous quest for alternative regimens. Deeper understanding of the pathogenesis of hepatitis C virus ushered in the era of direct acting antiviral agents. These agents have been the subject of intensive research in the last two decades, leading to the development of drug classes such as protease inhibitors (e.g., grazoprevir), NS5A inhibitors (e.g., daclatasvir) and NS5B inhibitors (e.g., sofosbuvir). While many are still under development, several have been approved for hepatitis C therapy. A number of studies investigating the combination of direct acting antiviral agents with or without pegylated interferon and/or ribavirin for the treatment of chronic hepatitis have demonstrated sustained virologic response of &gt; 90%. Given the array of direct acting antiviral agents currently available, the present landscape of hepatitis C therapy is now characterized by a gradual transition to all-oral interferon-free regimens. Despite these milestones, the WHO global target of eliminating hepatitis C as a public health problem by 2030 seems uncertain. In this review, we provide a concise account of the evolution and advancements in the development of anti-HCV regimens.</description><identifier>ISSN: 1972-2680</identifier><identifier>ISSN: 2036-6590</identifier><identifier>EISSN: 1972-2680</identifier><identifier>DOI: 10.3855/jidc.14485</identifier><identifier>PMID: 35298416</identifier><language>eng</language><publisher>Italy: Journal of Infection in Developing Countries</publisher><subject>Antiviral Agents - pharmacology ; Antiviral Agents - therapeutic use ; Hepacivirus - genetics ; Hepatitis C ; Hepatitis C - drug therapy ; Hepatitis C, Chronic - drug therapy ; Humans ; Interferon ; Interferon-alpha - therapeutic use</subject><ispartof>Journal of infection in developing countries, 2022-02, Vol.16 (2), p.231-243</ispartof><rights>Copyright (c) 2022 Ahmad Adebayo Irekeola, Engku Nur Syafirah EAR, Nur Amalin Zahirah Mohd Amin, Nazri Mustaffa, Rafidah Hanim Shueb.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-9978f98fb62faf8ac1b71c09c392eebd5ada6b88f8515520c8bb5f26bae183533</citedby><orcidid>0000-0003-3249-6357 ; 0000-0002-1779-9571</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3131776900?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>313,314,780,784,792,25752,27921,27923,27924,37011,37012,44589</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35298416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Irekeola, Ahmad Adebayo</creatorcontrib><creatorcontrib>Ear, Engku Nur Syafirah</creatorcontrib><creatorcontrib>Mohd Amin, Nur Amalin Zahirah</creatorcontrib><creatorcontrib>Mustaffa, Nazri</creatorcontrib><creatorcontrib>Shueb, Rafidah Hanim</creatorcontrib><title>Antivirals against HCV infection: the story thus far</title><title>Journal of infection in developing countries</title><addtitle>J Infect Dev Ctries</addtitle><description>Remarkable scientific breakthroughs have been made in the stride towards the development of potent and tolerable hepatitis C regimens within the last three decades. Earlier approaches involved the use of pegylated interferon alfa and ribavirin as standard-of-care treatment. Treating genotype 1a infection with this regimen which was at that time considered the gold standard for hepatitis C virus therapy was rife with challenges; safety and toxicity issues necessitated a rigorous quest for alternative regimens. Deeper understanding of the pathogenesis of hepatitis C virus ushered in the era of direct acting antiviral agents. These agents have been the subject of intensive research in the last two decades, leading to the development of drug classes such as protease inhibitors (e.g., grazoprevir), NS5A inhibitors (e.g., daclatasvir) and NS5B inhibitors (e.g., sofosbuvir). While many are still under development, several have been approved for hepatitis C therapy. A number of studies investigating the combination of direct acting antiviral agents with or without pegylated interferon and/or ribavirin for the treatment of chronic hepatitis have demonstrated sustained virologic response of &gt; 90%. Given the array of direct acting antiviral agents currently available, the present landscape of hepatitis C therapy is now characterized by a gradual transition to all-oral interferon-free regimens. Despite these milestones, the WHO global target of eliminating hepatitis C as a public health problem by 2030 seems uncertain. In this review, we provide a concise account of the evolution and advancements in the development of anti-HCV regimens.</description><subject>Antiviral Agents - pharmacology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis C</subject><subject>Hepatitis C - drug therapy</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Humans</subject><subject>Interferon</subject><subject>Interferon-alpha - therapeutic use</subject><issn>1972-2680</issn><issn>2036-6590</issn><issn>1972-2680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkMFKAzEURYMotlY3foAMuBFhal4ymUnclaJWKLhRtyHJJJrSztQkI_Tvndoq4urdxbmXx0HoHPCYcsZuFr42YygKzg7QEERFclJyfPgnD9BJjAuMmaAMjtGAMiJ4AeUQFZMm-U8f1DJm6k35JqZsNn3NfOOsSb5tbrP0brOY2rDpUxczp8IpOnJ9wZ7t7wi93N89T2f5_OnhcTqZ54YCS7kQFXeCO10SpxxXBnQFBgtDBbFW10zVqtScO86AMYIN15o5UmplgVNG6Qhd7XbXof3obExy5aOxy6VqbNtFScoCMIaiwj16-Q9dtF1o-u8kBQpVVQq8pa53lAltjME6uQ5-pcJGApZbl3LrUn677OGL_WSnV7b-RX_k0S9kjm3A</recordid><startdate>20220228</startdate><enddate>20220228</enddate><creator>Irekeola, Ahmad Adebayo</creator><creator>Ear, Engku Nur Syafirah</creator><creator>Mohd Amin, Nur Amalin Zahirah</creator><creator>Mustaffa, Nazri</creator><creator>Shueb, Rafidah Hanim</creator><general>Journal of Infection in Developing Countries</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8C1</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3249-6357</orcidid><orcidid>https://orcid.org/0000-0002-1779-9571</orcidid></search><sort><creationdate>20220228</creationdate><title>Antivirals against HCV infection: the story thus far</title><author>Irekeola, Ahmad Adebayo ; Ear, Engku Nur Syafirah ; Mohd Amin, Nur Amalin Zahirah ; Mustaffa, Nazri ; Shueb, Rafidah Hanim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-9978f98fb62faf8ac1b71c09c392eebd5ada6b88f8515520c8bb5f26bae183533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antiviral Agents - pharmacology</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Hepacivirus - genetics</topic><topic>Hepatitis C</topic><topic>Hepatitis C - drug therapy</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Humans</topic><topic>Interferon</topic><topic>Interferon-alpha - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Irekeola, Ahmad Adebayo</creatorcontrib><creatorcontrib>Ear, Engku Nur Syafirah</creatorcontrib><creatorcontrib>Mohd Amin, Nur Amalin Zahirah</creatorcontrib><creatorcontrib>Mustaffa, Nazri</creatorcontrib><creatorcontrib>Shueb, Rafidah Hanim</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Public Health Database</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of infection in developing countries</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Irekeola, Ahmad Adebayo</au><au>Ear, Engku Nur Syafirah</au><au>Mohd Amin, Nur Amalin Zahirah</au><au>Mustaffa, Nazri</au><au>Shueb, Rafidah Hanim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antivirals against HCV infection: the story thus far</atitle><jtitle>Journal of infection in developing countries</jtitle><addtitle>J Infect Dev Ctries</addtitle><date>2022-02-28</date><risdate>2022</risdate><volume>16</volume><issue>2</issue><spage>231</spage><epage>243</epage><pages>231-243</pages><issn>1972-2680</issn><issn>2036-6590</issn><eissn>1972-2680</eissn><abstract>Remarkable scientific breakthroughs have been made in the stride towards the development of potent and tolerable hepatitis C regimens within the last three decades. Earlier approaches involved the use of pegylated interferon alfa and ribavirin as standard-of-care treatment. Treating genotype 1a infection with this regimen which was at that time considered the gold standard for hepatitis C virus therapy was rife with challenges; safety and toxicity issues necessitated a rigorous quest for alternative regimens. Deeper understanding of the pathogenesis of hepatitis C virus ushered in the era of direct acting antiviral agents. These agents have been the subject of intensive research in the last two decades, leading to the development of drug classes such as protease inhibitors (e.g., grazoprevir), NS5A inhibitors (e.g., daclatasvir) and NS5B inhibitors (e.g., sofosbuvir). While many are still under development, several have been approved for hepatitis C therapy. A number of studies investigating the combination of direct acting antiviral agents with or without pegylated interferon and/or ribavirin for the treatment of chronic hepatitis have demonstrated sustained virologic response of &gt; 90%. Given the array of direct acting antiviral agents currently available, the present landscape of hepatitis C therapy is now characterized by a gradual transition to all-oral interferon-free regimens. Despite these milestones, the WHO global target of eliminating hepatitis C as a public health problem by 2030 seems uncertain. In this review, we provide a concise account of the evolution and advancements in the development of anti-HCV regimens.</abstract><cop>Italy</cop><pub>Journal of Infection in Developing Countries</pub><pmid>35298416</pmid><doi>10.3855/jidc.14485</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-3249-6357</orcidid><orcidid>https://orcid.org/0000-0002-1779-9571</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1972-2680
ispartof Journal of infection in developing countries, 2022-02, Vol.16 (2), p.231-243
issn 1972-2680
2036-6590
1972-2680
language eng
recordid cdi_proquest_miscellaneous_2641001470
source Publicly Available Content Database
subjects Antiviral Agents - pharmacology
Antiviral Agents - therapeutic use
Hepacivirus - genetics
Hepatitis C
Hepatitis C - drug therapy
Hepatitis C, Chronic - drug therapy
Humans
Interferon
Interferon-alpha - therapeutic use
title Antivirals against HCV infection: the story thus far
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T16%3A45%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antivirals%20against%20HCV%20infection:%20the%20story%20thus%20far&rft.jtitle=Journal%20of%20infection%20in%20developing%20countries&rft.au=Irekeola,%20Ahmad%20Adebayo&rft.date=2022-02-28&rft.volume=16&rft.issue=2&rft.spage=231&rft.epage=243&rft.pages=231-243&rft.issn=1972-2680&rft.eissn=1972-2680&rft_id=info:doi/10.3855/jidc.14485&rft_dat=%3Cproquest_cross%3E2641001470%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c315t-9978f98fb62faf8ac1b71c09c392eebd5ada6b88f8515520c8bb5f26bae183533%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3131776900&rft_id=info:pmid/35298416&rfr_iscdi=true