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dc.contributor.authorAtcheson, E
dc.contributor.authorLi, W
dc.contributor.authorBliss, CM
dc.contributor.authorChinnakannan, S
dc.contributor.authorHeim, K
dc.contributor.authorSharpe, H
dc.contributor.authorHutchings, C
dc.contributor.authorDietrich, I
dc.contributor.authorNguyen, D
dc.contributor.authorKapoor, A
dc.contributor.authorJarvis, Michael A
dc.contributor.authorKlenerman, P
dc.contributor.authorBarnes, E
dc.contributor.authorSimmonds, P
dc.date.accessioned2020-09-15T12:36:24Z
dc.date.issued2020-03
dc.identifier.issn0270-9139
dc.identifier.issn1527-3350
dc.identifier.urihttp://hdl.handle.net/10026.1/16343
dc.description.abstract

<jats:sec> <jats:title>Background and Aims</jats:title> <jats:p>The lack of immunocompetent small animal models for hepatitis C virus (HCV) has greatly hindered the development of effective vaccines. Using rodent hepacivirus (RHV), a homolog of HCV that shares many characteristics of HCV infection, we report the development and application of an RHV outbred rat model for HCV vaccine development.</jats:p> </jats:sec> <jats:sec> <jats:title>Approach and Results</jats:title> <jats:p>Simian adenovirus (ChAdOx1) encoding a genetic immune enhancer (truncated shark class II invariant chain) fused to the nonstructural (NS) proteins NS3‐NS5B from RHV (ChAd‐NS) was used to vaccinate Sprague‐Dawley rats, resulting in high levels of cluster of differentiation 8–positive (CD8<jats:sup>+</jats:sup>) T‐cell responses. Following RHV challenge (using 10 or 100 times the minimum infectious dose), 42% of vaccinated rats cleared infection within 6‐8 weeks, while all mock vaccinated controls became infected with high‐level viremia postchallenge. A single, 7‐fold higher dose of ChAd‐NS increased efficacy to 67%. Boosting with ChAd‐NS or with a plasmid encoding the same NS3‐NS5B antigens increased efficacy to 100% and 83%, respectively. A ChAdOx1 vector encoding structural antigens (ChAd‐S) was also constructed. ChAd‐S alone showed no efficacy. Strikingly, when combined with ChAd‐NS, ChAD‐S produced 83% efficacy. Protection was associated with a strong CD8<jats:sup>+</jats:sup> interferon gamma–positive recall response against NS4. Next‐generation sequencing of a putative RHV escape mutant in a vaccinated rat identified mutations in both identified immunodominant CD8<jats:sup>+</jats:sup> T‐cell epitopes.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>A simian adenovirus vector vaccine strategy is effective at inducing complete protective immunity in the rat RHV model. The RHV Sprague‐Dawley rat challenge model enables comparative testing of vaccine platforms and antigens and identification of correlates of protection and thereby provides a small animal experimental framework to guide the development of an effective vaccine for HCV in humans.</jats:p> </jats:sec>

dc.format.extent794-807
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherWiley
dc.subjectAdenoviridae
dc.subjectAnimals
dc.subjectCD8-Positive T-Lymphocytes
dc.subjectDisease Models, Animal
dc.subjectEpitopes, T-Lymphocyte
dc.subjectHepacivirus
dc.subjectInterferon-gamma
dc.subjectMale
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectVaccination
dc.subjectVaccines, Synthetic
dc.subjectViral Hepatitis Vaccines
dc.subjectViral Nonstructural Proteins
dc.titleUse of an Outbred Rat Hepacivirus Challenge Model for Design and Evaluation of Efficacy of Different Immunization Strategies for Hepatitis C Virus
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000489670300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue3
plymouth.volume71
plymouth.publication-statusPublished
plymouth.journalHepatology
dc.identifier.doi10.1002/hep.30894
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2019-08-05
dc.rights.embargodate2020-9-19
dc.identifier.eissn1527-3350
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1002/hep.30894
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-03
rioxxterms.typeJournal Article/Review


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