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A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice
Recombinant Salmonella enterica serovar Typhi can function as a live vector to deliver foreign antigens to the mammalian immune system and induce both mucosal and systemic immunity. In this study, we generated a recombinant Salmonella Typhi strain pilS(−)pilT(−)Gag(+)(pVAX1-gp120) harboring the huma...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114238/ https://www.ncbi.nlm.nih.gov/pubmed/18639586 http://dx.doi.org/10.1016/j.antiviral.2008.06.013 |
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author | Feng, Yong Wang, Shiqun Luo, Fenglin Ruan, Ying Kang, Lei Xiang, Xiaohui Chao, Tao Peng, Guiqing Zhu, Chengliang Mu, Yongxin Zhu, Ying Zhang, Xiaolian Wu, Jianguo |
author_facet | Feng, Yong Wang, Shiqun Luo, Fenglin Ruan, Ying Kang, Lei Xiang, Xiaohui Chao, Tao Peng, Guiqing Zhu, Chengliang Mu, Yongxin Zhu, Ying Zhang, Xiaolian Wu, Jianguo |
author_sort | Feng, Yong |
collection | PubMed |
description | Recombinant Salmonella enterica serovar Typhi can function as a live vector to deliver foreign antigens to the mammalian immune system and induce both mucosal and systemic immunity. In this study, we generated a recombinant Salmonella Typhi strain pilS(−)pilT(−)Gag(+)(pVAX1-gp120) harboring the human immunodeficiency virus (HIV) gag gene integrated into the bacterial chromosome and gp120 gene carried by a plasmid. Mice inoculated with this recombinant bacterium through intranasal route produced high titers of IgG to gp120 in sera and IgA to gp120 in fecal washes. In addition, Gag-specific and gp120-specific cytotoxic T lymphocyte (CTL) responses were observed in sorted spleen lymphocytes of immunized mice. These results demonstrated that this recombinant Salmonella Typhi strain elicits multiple immune responses against both Gag and gp120 antigens of HIV, and thus would be a potential vaccine candidate to the prevention of HIV/AIDS. |
format | Online Article Text |
id | pubmed-7114238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71142382020-04-02 A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice Feng, Yong Wang, Shiqun Luo, Fenglin Ruan, Ying Kang, Lei Xiang, Xiaohui Chao, Tao Peng, Guiqing Zhu, Chengliang Mu, Yongxin Zhu, Ying Zhang, Xiaolian Wu, Jianguo Antiviral Res Article Recombinant Salmonella enterica serovar Typhi can function as a live vector to deliver foreign antigens to the mammalian immune system and induce both mucosal and systemic immunity. In this study, we generated a recombinant Salmonella Typhi strain pilS(−)pilT(−)Gag(+)(pVAX1-gp120) harboring the human immunodeficiency virus (HIV) gag gene integrated into the bacterial chromosome and gp120 gene carried by a plasmid. Mice inoculated with this recombinant bacterium through intranasal route produced high titers of IgG to gp120 in sera and IgA to gp120 in fecal washes. In addition, Gag-specific and gp120-specific cytotoxic T lymphocyte (CTL) responses were observed in sorted spleen lymphocytes of immunized mice. These results demonstrated that this recombinant Salmonella Typhi strain elicits multiple immune responses against both Gag and gp120 antigens of HIV, and thus would be a potential vaccine candidate to the prevention of HIV/AIDS. Elsevier B.V. 2008-12 2008-07-17 /pmc/articles/PMC7114238/ /pubmed/18639586 http://dx.doi.org/10.1016/j.antiviral.2008.06.013 Text en Copyright © 2008 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Feng, Yong Wang, Shiqun Luo, Fenglin Ruan, Ying Kang, Lei Xiang, Xiaohui Chao, Tao Peng, Guiqing Zhu, Chengliang Mu, Yongxin Zhu, Ying Zhang, Xiaolian Wu, Jianguo A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title | A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title_full | A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title_fullStr | A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title_full_unstemmed | A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title_short | A novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the Gag and gp120 proteins of HIV-1 in immunized mice |
title_sort | novel recombinant bacterial vaccine strain expressing dual viral antigens induces multiple immune responses to the gag and gp120 proteins of hiv-1 in immunized mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114238/ https://www.ncbi.nlm.nih.gov/pubmed/18639586 http://dx.doi.org/10.1016/j.antiviral.2008.06.013 |
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