P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice
| dc.contributor.author | Stutz, H | en_ZA |
| dc.contributor.author | Powles, R | en_ZA |
| dc.contributor.author | Shephard, EG | en_ZA |
| dc.contributor.author | Williamson, A | en_ZA |
| dc.date.accessioned | 2015-11-04T11:45:19Z | |
| dc.date.available | 2015-11-04T11:45:19Z | |
| dc.date.issued | 2009 | en_ZA |
| dc.description.abstract | Mycobacterium bovis BCG (BCG) has a number of characteristics that give it great potential to act as a vehicle for the delivery of recombinant vaccines. However, its success depends on overcoming the challenges of poor antigen expression levels and genetic instability. Our studies using an optimized mycobacterial shuttle vector which utilizes the Mycobacterium tuberculosis mtrA promoter, induced upon infection of macrophages, and the M. tuberculosis 19 kDa signal sequence may overcome these issues. We have used this system to generate a recombinant BCG (rBCG) expressing HIV-1 subtype C full length Gag or reverse transcriptase (RT). | en_ZA |
| dc.identifier.apacitation | Stutz, H., Powles, R., Shephard, E., & Williamson, A. (2009). P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice. <i>Retrovirology</i>, http://hdl.handle.net/11427/14656 | en_ZA |
| dc.identifier.chicagocitation | Stutz, H, R Powles, EG Shephard, and A Williamson "P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice." <i>Retrovirology</i> (2009) http://hdl.handle.net/11427/14656 | en_ZA |
| dc.identifier.citation | Stutz, H., Powles, R., Shephard, E. G., & Williamson, A. (2009). P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice. Retrovirology, 6(Suppl 3), P417. | en_ZA |
| dc.identifier.ris | TY - Journal Article AU - Stutz, H AU - Powles, R AU - Shephard, EG AU - Williamson, A AB - Mycobacterium bovis BCG (BCG) has a number of characteristics that give it great potential to act as a vehicle for the delivery of recombinant vaccines. However, its success depends on overcoming the challenges of poor antigen expression levels and genetic instability. Our studies using an optimized mycobacterial shuttle vector which utilizes the Mycobacterium tuberculosis mtrA promoter, induced upon infection of macrophages, and the M. tuberculosis 19 kDa signal sequence may overcome these issues. We have used this system to generate a recombinant BCG (rBCG) expressing HIV-1 subtype C full length Gag or reverse transcriptase (RT). DA - 2009 DB - OpenUCT DO - 10.1186/1742-4690-6-S3-P417 DP - University of Cape Town J1 - Retrovirology LK - https://open.uct.ac.za PB - University of Cape Town PY - 2009 T1 - P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice TI - P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice UR - http://hdl.handle.net/11427/14656 ER - | en_ZA |
| dc.identifier.uri | http://hdl.handle.net/11427/14656 | |
| dc.identifier.uri | http://dx.doi.org/10.1186/1742-4690-6-S3-P417 | |
| dc.identifier.vancouvercitation | Stutz H, Powles R, Shephard E, Williamson A. P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice. Retrovirology. 2009; http://hdl.handle.net/11427/14656. | en_ZA |
| dc.language.iso | eng | en_ZA |
| dc.publisher | BioMed Central Ltd | en_ZA |
| dc.publisher.department | Division of Medical Microbiology | en_ZA |
| dc.publisher.faculty | Faculty of Health Sciences | en_ZA |
| dc.publisher.institution | University of Cape Town | |
| dc.rights | This is an Open Access article distributed under the terms of the Creative Commons Attribution License | en_ZA |
| dc.rights.holder | 2009 Stutz et al; licensee BioMed Central Ltd. | en_ZA |
| dc.rights.uri | http://creativecommons.org/licenses/by/2.0 | en_ZA |
| dc.source | Retrovirology | en_ZA |
| dc.source.uri | http://www.retrovirology.com/ | en_ZA |
| dc.subject.other | Wild Type BCG | en_ZA |
| dc.subject.other | Booster Vaccine | en_ZA |
| dc.subject.other | Antigen Specific CD8 | en_ZA |
| dc.subject.other | Primary Vaccine | en_ZA |
| dc.subject.other | rBCG Vaccine | en_ZA |
| dc.subject.other | ELISPOT Assay | en_ZA |
| dc.title | P19-53 LB. Priming with recombinant BCG expressing HIV-1 Gag or RT and boosting with recombinant MVA induces an effective immune response in mice | en_ZA |
| dc.type | Journal Article | en_ZA |
| uct.type.filetype | Text | |
| uct.type.filetype | Image | |
| uct.type.publication | Research | en_ZA |
| uct.type.resource | Article | en_ZA |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- Stutz_P19_53_LB_Priming_recombinant_BCG_2009.pdf
- Size:
- 66.86 KB
- Format:
- Adobe Portable Document Format
- Description: