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- Publisher Website: 10.1186/1743-422X-7-9
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- PMID: 20082709
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Article: An M2e-based multiple antigenic peptide vaccine protects mice from lethal challenge with divergent H5N1 influenza viruses
Title | An M2e-based multiple antigenic peptide vaccine protects mice from lethal challenge with divergent H5N1 influenza viruses | ||||||||||||||
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Authors | |||||||||||||||
Issue Date | 2010 | ||||||||||||||
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.virologyj.com/home/ | ||||||||||||||
Citation | Virology Journal, 2010, v. 7 How to Cite? | ||||||||||||||
Abstract | Background. A growing concern has raised regarding the pandemic potential of the highly pathogenic avian influenza (HPAI) H5N1 viruses. Consequently, there is an urgent need to develop an effective and safe vaccine against the divergent H5N1 influenza viruses. In the present study, we designed a tetra-branched multiple antigenic peptide (MAP)-based vaccine, designated M2e-MAP, which contains the sequence overlapping the highly conserved extracellular domain of matrix protein 2 (M2e) of a HPAI H5N1 virus, and investigated its immune responses and cross-protection against different clades of H5N1 viruses. Results. Our results showed that M2e-MAP vaccine induced strong M2e-specific IgG antibody responses following 3-dose immunization of mice with M2e-MAP in the presence of Freunds' or aluminium (alum) adjuvant. M2e-MAP vaccination limited viral replication and attenuated histopathological damage in the challenged mouse lungs. The M2e-MAP-based vaccine protected immunized mice against both clade1: VN/1194 and clade2.3.4: SZ/406H H5N1 virus challenge, being able to counteract weight lost and elevate survival rate following lethal challenge of H5N1 viruses. Conclusions. These results suggest that M2e-MAP presenting M2e of H5N1 virus has a great potential to be developed into an effective subunit vaccine for the prevention of infection by a broad spectrum of HPAI H5N1 viruses. © 2010 Zhao et al; licensee BioMed Central Ltd. | ||||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/125131 | ||||||||||||||
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.016 | ||||||||||||||
PubMed Central ID | |||||||||||||||
ISI Accession Number ID |
Funding Information: This study was supported by the National High Technology R&D Program of China (863 Program, No. 2006AA02Z406), National Basic Research Program of China (973 Program, No. 2005CB523001), National Natural Science Foundation of China (30901371), Mega-projects of Science Research for the 11th Five-Year Plan (2009ZX10004-4001), the Area of Excellence Scheme of the University Grants Committee (Grant AoE/M-12/06) and Research Fund for the Control of Infectious Diseases (09080812), Hong Kong SAR. | ||||||||||||||
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Grants |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhao, G | en_HK |
dc.contributor.author | Lin, Y | en_HK |
dc.contributor.author | Du, L | en_HK |
dc.contributor.author | Guan, J | en_HK |
dc.contributor.author | Sun, S | en_HK |
dc.contributor.author | Sui, H | en_HK |
dc.contributor.author | Kou, Z | en_HK |
dc.contributor.author | Chan, CC | en_HK |
dc.contributor.author | Guo, Y | en_HK |
dc.contributor.author | Jiang, S | en_HK |
dc.contributor.author | Zheng, BJ | en_HK |
dc.contributor.author | Zhou, Y | en_HK |
dc.date.accessioned | 2010-10-31T11:13:09Z | - |
dc.date.available | 2010-10-31T11:13:09Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Virology Journal, 2010, v. 7 | en_HK |
dc.identifier.issn | 1743-422X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/125131 | - |
dc.description.abstract | Background. A growing concern has raised regarding the pandemic potential of the highly pathogenic avian influenza (HPAI) H5N1 viruses. Consequently, there is an urgent need to develop an effective and safe vaccine against the divergent H5N1 influenza viruses. In the present study, we designed a tetra-branched multiple antigenic peptide (MAP)-based vaccine, designated M2e-MAP, which contains the sequence overlapping the highly conserved extracellular domain of matrix protein 2 (M2e) of a HPAI H5N1 virus, and investigated its immune responses and cross-protection against different clades of H5N1 viruses. Results. Our results showed that M2e-MAP vaccine induced strong M2e-specific IgG antibody responses following 3-dose immunization of mice with M2e-MAP in the presence of Freunds' or aluminium (alum) adjuvant. M2e-MAP vaccination limited viral replication and attenuated histopathological damage in the challenged mouse lungs. The M2e-MAP-based vaccine protected immunized mice against both clade1: VN/1194 and clade2.3.4: SZ/406H H5N1 virus challenge, being able to counteract weight lost and elevate survival rate following lethal challenge of H5N1 viruses. Conclusions. These results suggest that M2e-MAP presenting M2e of H5N1 virus has a great potential to be developed into an effective subunit vaccine for the prevention of infection by a broad spectrum of HPAI H5N1 viruses. © 2010 Zhao et al; licensee BioMed Central Ltd. | en_HK |
dc.language | eng | en_HK |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.virologyj.com/home/ | en_HK |
dc.relation.ispartof | Virology Journal | en_HK |
dc.rights | Virology Journal. Copyright © BioMed Central Ltd. | - |
dc.subject.mesh | Adjuvants, Immunologic - administration and dosage | - |
dc.subject.mesh | Antigens, Viral - immunology | - |
dc.subject.mesh | Influenza A Virus, H5N1 Subtype - immunology | - |
dc.subject.mesh | Influenza Vaccines - immunology | - |
dc.subject.mesh | Viral Matrix Proteins - immunology | - |
dc.title | An M2e-based multiple antigenic peptide vaccine protects mice from lethal challenge with divergent H5N1 influenza viruses | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1743-422X&volume=7&issue=article no. 9&spage=&epage=&date=2010&atitle=An+M2e-based+multiple+antigenic+peptide+vaccine+protects+mice+from+lethal+challenge+with+divergent+H5N1+influenza+viruses | - |
dc.identifier.email | Zheng, BJ:bzheng@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zheng, BJ=rp00353 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/1743-422X-7-9 | en_HK |
dc.identifier.pmid | 20082709 | en_HK |
dc.identifier.pmcid | PMC2823673 | - |
dc.identifier.scopus | eid_2-s2.0-77249104563 | en_HK |
dc.identifier.hkuros | 175099 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77249104563&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 7 | en_HK |
dc.identifier.issue | article no. 9 | en_HK |
dc.identifier.eissn | 1743-422X | - |
dc.identifier.isi | WOS:000275091300001 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.relation.project | Cross-protective efficacy of immunization with different forms of M2 vaccines and their combinations with HA vaccines against highly pathogenic H5N1 influenza A viruses in mice | - |
dc.relation.project | Control of Pandemic and Inter-pandemic Influenza | - |
dc.identifier.scopusauthorid | Zhao, G=8684553000 | en_HK |
dc.identifier.scopusauthorid | Lin, Y=8591935100 | en_HK |
dc.identifier.scopusauthorid | Du, L=8686996200 | en_HK |
dc.identifier.scopusauthorid | Guan, J=35573273400 | en_HK |
dc.identifier.scopusauthorid | Sun, S=35171536200 | en_HK |
dc.identifier.scopusauthorid | Sui, H=23971615600 | en_HK |
dc.identifier.scopusauthorid | Kou, Z=23034818200 | en_HK |
dc.identifier.scopusauthorid | Chan, CC=36984588300 | en_HK |
dc.identifier.scopusauthorid | Guo, Y=8555122500 | en_HK |
dc.identifier.scopusauthorid | Jiang, S=7404453146 | en_HK |
dc.identifier.scopusauthorid | Zheng, BJ=7201780588 | en_HK |
dc.identifier.scopusauthorid | Zhou, Y=8791655300 | en_HK |
dc.identifier.citeulike | 6564277 | - |
dc.identifier.issnl | 1743-422X | - |