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Article: A Replicating Modified Vaccinia Tiantan Strain Expressing an Avian-Derived Influenza H5N1 Hemagglutinin Induce Broadly Neutralizing Antibodies and Cross-Clade Protective Immunity in Mice

TitleA Replicating Modified Vaccinia Tiantan Strain Expressing an Avian-Derived Influenza H5N1 Hemagglutinin Induce Broadly Neutralizing Antibodies and Cross-Clade Protective Immunity in Mice
Authors
Issue Date2013
PublisherPublic Library of Science. The Journal's web site is located at http://www.plosone.org/home.action
Citation
PLoS ONE, 2013, v. 8 n. 12, article no. e83274 How to Cite?
AbstractTo combat the possibility of a zoonotic H5N1 pandemic in a timely fashion, it is necessary to develop a vaccine that would confer protection against homologous and heterologous human H5N1 influenza viruses. Using a replicating modified vaccinia virus Tian Tan strain (MVTT) as a vaccine vector, we constructed MVTTHA-QH and MVTTHA-AH, which expresses the H5 gene of a goose-derived Qinghai strain A/Bar-headed Goose/Qinghai/1/2005 or human-derived Anhui Strain A/Anhui/1/2005. The immunogenicity profiles of both vaccine candidates were evaluated. Vaccination with MVTTHA-QH induced a significant level of neutralizing antibodies (Nabs) against a homologous strain and a wide range of H5N1 pseudoviruses (clades 1, 2.1, 2.2, 2.3.2, and 2.3.4). Neutralization tests (NT) and Haemagglutination inhibition (HI) antibodies inhibit the live autologous virus as well as a homologous A/Xingjiang/1/2006 and a heterologous A/Vietnam/1194/2004, representing two human isolates from clade 2.2 and clade 1, respectively. Importantly, mice vaccinated with intranasal MVTTHA-QH were completely protected from challenge with lethal dosages of A/Bar-headed Goose/Qinghai/1/2005 and the A/Viet Nam/1194/2004, respectively, but not control mice that received a mock MVTTS vaccine. However, MVTTHA-AH induced much lower levels of NT against its autologous strain. Our results suggest that it is feasible to use the H5 gene from A/Bar-headed Goose/Qinghai/1/2005 to construct an effective vaccine, when using MVTT as a vector, to prevent infections against homologous and genetically divergent human H5N1 influenza viruses.
Persistent Identifierhttp://hdl.handle.net/10722/203172
PubMed Central ID
ISI Accession Number ID
Errata

 

DC FieldValueLanguage
dc.contributor.authorXiao, Hen_US
dc.contributor.authorLiu, Len_US
dc.contributor.authorZhu, Qen_US
dc.contributor.authorTan, Zen_US
dc.contributor.authorYu, Wen_US
dc.contributor.authorTang, Xen_US
dc.contributor.authorZhan, Den_US
dc.contributor.authorDu, Yen_US
dc.contributor.authorWang, Hen_US
dc.contributor.authorLiu, Den_US
dc.contributor.authorLi, Zen_US
dc.contributor.authorYuen, KYen_US
dc.contributor.authorHo, DDen_US
dc.contributor.authorGao, GFen_US
dc.contributor.authorChen, Zen_US
dc.date.accessioned2014-09-19T12:56:44Z-
dc.date.available2014-09-19T12:56:44Z-
dc.date.issued2013en_US
dc.identifier.citationPLoS ONE, 2013, v. 8 n. 12, article no. e83274en_US
dc.identifier.urihttp://hdl.handle.net/10722/203172-
dc.description.abstractTo combat the possibility of a zoonotic H5N1 pandemic in a timely fashion, it is necessary to develop a vaccine that would confer protection against homologous and heterologous human H5N1 influenza viruses. Using a replicating modified vaccinia virus Tian Tan strain (MVTT) as a vaccine vector, we constructed MVTTHA-QH and MVTTHA-AH, which expresses the H5 gene of a goose-derived Qinghai strain A/Bar-headed Goose/Qinghai/1/2005 or human-derived Anhui Strain A/Anhui/1/2005. The immunogenicity profiles of both vaccine candidates were evaluated. Vaccination with MVTTHA-QH induced a significant level of neutralizing antibodies (Nabs) against a homologous strain and a wide range of H5N1 pseudoviruses (clades 1, 2.1, 2.2, 2.3.2, and 2.3.4). Neutralization tests (NT) and Haemagglutination inhibition (HI) antibodies inhibit the live autologous virus as well as a homologous A/Xingjiang/1/2006 and a heterologous A/Vietnam/1194/2004, representing two human isolates from clade 2.2 and clade 1, respectively. Importantly, mice vaccinated with intranasal MVTTHA-QH were completely protected from challenge with lethal dosages of A/Bar-headed Goose/Qinghai/1/2005 and the A/Viet Nam/1194/2004, respectively, but not control mice that received a mock MVTTS vaccine. However, MVTTHA-AH induced much lower levels of NT against its autologous strain. Our results suggest that it is feasible to use the H5 gene from A/Bar-headed Goose/Qinghai/1/2005 to construct an effective vaccine, when using MVTT as a vector, to prevent infections against homologous and genetically divergent human H5N1 influenza viruses.-
dc.languageengen_US
dc.publisherPublic Library of Science. The Journal's web site is located at http://www.plosone.org/home.action-
dc.relation.ispartofPLoS ONEen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleA Replicating Modified Vaccinia Tiantan Strain Expressing an Avian-Derived Influenza H5N1 Hemagglutinin Induce Broadly Neutralizing Antibodies and Cross-Clade Protective Immunity in Miceen_US
dc.typeArticleen_US
dc.identifier.emailLiu, L: liuli71@hkucc.hku.hken_US
dc.identifier.emailDu, DY: biodu@hku.hken_US
dc.identifier.emailWang, H: hbwang@hkucc.hku.hken_US
dc.identifier.emailYuen, KY: kyyuen@hkucc.hku.hken_US
dc.identifier.emailChen, Z: zchenai@hku.hken_US
dc.identifier.authorityLiu, L=rp00268en_US
dc.identifier.authorityYuen, KY=rp00366en_US
dc.identifier.authorityChen, Z=rp00243en_US
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1371/journal.pone.0083274en_US
dc.identifier.pmid24358269-
dc.identifier.pmcidPMC3866202-
dc.identifier.scopuseid_2-s2.0-84892924704-
dc.identifier.hkuros237094en_US
dc.identifier.volume8en_US
dc.identifier.issue12-
dc.identifier.spagearticle no. e83274-
dc.identifier.epagearticle no. e83274-
dc.identifier.eissn1932-6203-
dc.identifier.isiWOS:000328737700055-
dc.relation.erratumdoi:10.1371/journal.pone.0115925-
dc.relation.erratumeid:eid_2-s2.0-84917691152-
dc.identifier.issnl1932-6203-

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