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- Publisher Website: 10.1016/j.bbrc.2004.01.166
- Scopus: eid_2-s2.0-1342324072
- PMID: 14985131
- WOS: WOS:000220105600053
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Article: Characterization of humoral responses in mice immunized with plasmid DNAs encoding SARS-CoV spike gene fragments
Title | Characterization of humoral responses in mice immunized with plasmid DNAs encoding SARS-CoV spike gene fragments |
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Authors | |
Keywords | Coronavirus DNA vaccine Neutralizing antibody SARS Spike glycoprotein |
Issue Date | 2004 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description |
Citation | Biochemical And Biophysical Research Communications, 2004, v. 315 n. 4, p. 1134-1139 How to Cite? |
Abstract | The immunological characteristics of SARS-CoV spike protein were investigated by administering mice with plasmids encoding various S gene fragments. We showed that the secreting forms of S1, S2 subunits and the N-terminus of S1 subunit (residues 18-495) were capable of eliciting SARS-CoV specific antibodies and the region immediate to N-terminus of matured S1 protein contained an important immunogenic determinant for elicitation of SARS-CoV specific antibodies. In addition, mice immunized with plasmids encoding S1 fragment developed a Th1-mediated antibody isotype switching. Another interesting finding was that mouse antibodies elicited separately by plasmids encoding S1 and S2 subunits cooperatively neutralized SARS-CoV but neither the S1 nor S2 specific antibodies did, suggesting the possible role of both S1 and S2 subunits in host cell docking and entry. These results provide insights into understanding the immunological characteristics of spike protein and the development of subunit vaccines against SARS-CoV. © 2004 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/78992 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.770 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Zeng, F | en_HK |
dc.contributor.author | Chow, KYC | en_HK |
dc.contributor.author | Hon, CC | en_HK |
dc.contributor.author | Law, KM | en_HK |
dc.contributor.author | Yip, CW | en_HK |
dc.contributor.author | Chan, KH | en_HK |
dc.contributor.author | Peiris, JSM | en_HK |
dc.contributor.author | Leung, FCC | en_HK |
dc.date.accessioned | 2010-09-06T07:49:17Z | - |
dc.date.available | 2010-09-06T07:49:17Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Biochemical And Biophysical Research Communications, 2004, v. 315 n. 4, p. 1134-1139 | en_HK |
dc.identifier.issn | 0006-291X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/78992 | - |
dc.description.abstract | The immunological characteristics of SARS-CoV spike protein were investigated by administering mice with plasmids encoding various S gene fragments. We showed that the secreting forms of S1, S2 subunits and the N-terminus of S1 subunit (residues 18-495) were capable of eliciting SARS-CoV specific antibodies and the region immediate to N-terminus of matured S1 protein contained an important immunogenic determinant for elicitation of SARS-CoV specific antibodies. In addition, mice immunized with plasmids encoding S1 fragment developed a Th1-mediated antibody isotype switching. Another interesting finding was that mouse antibodies elicited separately by plasmids encoding S1 and S2 subunits cooperatively neutralized SARS-CoV but neither the S1 nor S2 specific antibodies did, suggesting the possible role of both S1 and S2 subunits in host cell docking and entry. These results provide insights into understanding the immunological characteristics of spike protein and the development of subunit vaccines against SARS-CoV. © 2004 Elsevier Inc. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description | en_HK |
dc.relation.ispartof | Biochemical and Biophysical Research Communications | en_HK |
dc.subject | Coronavirus | en_HK |
dc.subject | DNA vaccine | en_HK |
dc.subject | Neutralizing antibody | en_HK |
dc.subject | SARS | en_HK |
dc.subject | Spike glycoprotein | en_HK |
dc.title | Characterization of humoral responses in mice immunized with plasmid DNAs encoding SARS-CoV spike gene fragments | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0006-291X&volume=315&spage=1134&epage=1139&date=2004&atitle=Characterization+of+humoral+responses+in+mice+immunized+with+plasmid+DNAs+encoding+SARS-CoV+spike+gene+fragments | en_HK |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | en_HK |
dc.identifier.email | Leung, FCC: fcleung@hkucc.hku.hk | en_HK |
dc.identifier.authority | Peiris, JSM=rp00410 | en_HK |
dc.identifier.authority | Leung, FCC=rp00731 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.bbrc.2004.01.166 | en_HK |
dc.identifier.pmid | 14985131 | - |
dc.identifier.scopus | eid_2-s2.0-1342324072 | en_HK |
dc.identifier.hkuros | 85670 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-1342324072&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 315 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 1134 | en_HK |
dc.identifier.epage | 1139 | en_HK |
dc.identifier.isi | WOS:000220105600053 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Zeng, F=7202911544 | en_HK |
dc.identifier.scopusauthorid | Chow, KYC=7202180875 | en_HK |
dc.identifier.scopusauthorid | Hon, CC=7003617137 | en_HK |
dc.identifier.scopusauthorid | Law, KM=7202563042 | en_HK |
dc.identifier.scopusauthorid | Yip, CW=7101665559 | en_HK |
dc.identifier.scopusauthorid | Chan, KH=7406034307 | en_HK |
dc.identifier.scopusauthorid | Peiris, JSM=7005486823 | en_HK |
dc.identifier.scopusauthorid | Leung, FCC=7103078633 | en_HK |
dc.identifier.issnl | 0006-291X | - |