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Article: Study on hybridized yeast-based HIV vaccine
Title | Study on hybridized yeast-based HIV vaccine |
---|---|
Authors | |
Keywords | Gene Engineering Hiv Vaccine Yeast Hybridization |
Issue Date | 2006 |
Citation | Chinese Journal Of Microbiology And Immunology, 2006, v. 26 n. 11, p. 1033-1037 How to Cite? |
Abstract | Objective: To perform pre-clinical study on a yeast-based HIV vaccine. Methods: Plasmids expressing Gag and IL-2 was respectively constructed and then transformed into yeast; yeast hybridization was performed to obtain yeast hybrid concurrently expressing Gag and IL-2; culture of yeast hybrid in large scale was performed. The final vaccine product was obtained through series of process including inactivation, lyophilization and filling. The efficacy and safety of the vaccine was analyzed in mouse and macaque models. Results: Expression of Gag and IL-2 in yeast hybrid is stable. Upon subcutaneous injection, HIV vaccine derived from the yeast hybrid could elicit strong Gag-specific cellular immune responses in mice and in macaque models, respectively. In addition, vaccine could also elicit strong protection from tumor challenge in mice. Study on safety indicated that, except for slight tenderness and swelling at the site of injection, there was no obvious acute as well as chronic toxicity. Conclusion: Yeast hybrid can be used as a vehicle for vaccine; yeast hybrid-based vaccine is capable of inducing strong antigen-specific cellular immune responses. Our studies imply that yeast hybrid is a promising vector and delivery system for the development of novel therapeutic vaccine candidates against infections and tumors. |
Persistent Identifier | http://hdl.handle.net/10722/157473 |
ISSN | 2023 SCImago Journal Rankings: 0.114 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhang, SE | en_US |
dc.contributor.author | Xiong, Q | en_US |
dc.contributor.author | Tang, HB | en_US |
dc.contributor.author | Liu, JY | en_US |
dc.contributor.author | Wu, YY | en_US |
dc.contributor.author | Wu, DP | en_US |
dc.contributor.author | Tian, WZ | en_US |
dc.contributor.author | Lu, JH | en_US |
dc.contributor.author | Zheng, BJ | en_US |
dc.contributor.author | Sun, J | en_US |
dc.date.accessioned | 2012-08-08T08:50:16Z | - |
dc.date.available | 2012-08-08T08:50:16Z | - |
dc.date.issued | 2006 | en_US |
dc.identifier.citation | Chinese Journal Of Microbiology And Immunology, 2006, v. 26 n. 11, p. 1033-1037 | en_US |
dc.identifier.issn | 0254-5101 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/157473 | - |
dc.description.abstract | Objective: To perform pre-clinical study on a yeast-based HIV vaccine. Methods: Plasmids expressing Gag and IL-2 was respectively constructed and then transformed into yeast; yeast hybridization was performed to obtain yeast hybrid concurrently expressing Gag and IL-2; culture of yeast hybrid in large scale was performed. The final vaccine product was obtained through series of process including inactivation, lyophilization and filling. The efficacy and safety of the vaccine was analyzed in mouse and macaque models. Results: Expression of Gag and IL-2 in yeast hybrid is stable. Upon subcutaneous injection, HIV vaccine derived from the yeast hybrid could elicit strong Gag-specific cellular immune responses in mice and in macaque models, respectively. In addition, vaccine could also elicit strong protection from tumor challenge in mice. Study on safety indicated that, except for slight tenderness and swelling at the site of injection, there was no obvious acute as well as chronic toxicity. Conclusion: Yeast hybrid can be used as a vehicle for vaccine; yeast hybrid-based vaccine is capable of inducing strong antigen-specific cellular immune responses. Our studies imply that yeast hybrid is a promising vector and delivery system for the development of novel therapeutic vaccine candidates against infections and tumors. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Chinese Journal of Microbiology and Immunology | en_US |
dc.subject | Gene Engineering | en_US |
dc.subject | Hiv | en_US |
dc.subject | Vaccine | en_US |
dc.subject | Yeast Hybridization | en_US |
dc.title | Study on hybridized yeast-based HIV vaccine | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zheng, BJ:bzheng@hkucc.hku.hk | en_US |
dc.identifier.authority | Zheng, BJ=rp00353 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.scopus | eid_2-s2.0-33847034839 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33847034839&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 26 | en_US |
dc.identifier.issue | 11 | en_US |
dc.identifier.spage | 1033 | en_US |
dc.identifier.epage | 1037 | en_US |
dc.identifier.scopusauthorid | Zhang, SE=15849864200 | en_US |
dc.identifier.scopusauthorid | Xiong, Q=55222654600 | en_US |
dc.identifier.scopusauthorid | Tang, HB=15849485200 | en_US |
dc.identifier.scopusauthorid | Liu, JY=26651214700 | en_US |
dc.identifier.scopusauthorid | Wu, YY=15849886300 | en_US |
dc.identifier.scopusauthorid | Wu, DP=15849818600 | en_US |
dc.identifier.scopusauthorid | Tian, WZ=55137435500 | en_US |
dc.identifier.scopusauthorid | Lu, JH=8079348400 | en_US |
dc.identifier.scopusauthorid | Zheng, BJ=7201780588 | en_US |
dc.identifier.scopusauthorid | Sun, J=37071291400 | en_US |
dc.identifier.issnl | 0254-5101 | - |