Cargando…

Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses

A safe and effective adjuvant is necessary to induce reliable protective efficacy of the protein-based vaccines against tuberculosis (TB). Mycobacterial components, such as synthetic cord factor and arabinogalactan, have been used as one of the adjuvant components. Mycobacterium bovis bacillus Calme...

Descripción completa

Detalles Bibliográficos
Autores principales: Back, Yong Woo, Choi, Seunga, Choi, Han-Gyu, Shin, Ki-Won, Son, Yeo-Jin, Paik, Tae-Hyun, Kim, Hwa-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407753/
https://www.ncbi.nlm.nih.gov/pubmed/30849108
http://dx.doi.org/10.1371/journal.pone.0213536
_version_ 1783401620988493824
author Back, Yong Woo
Choi, Seunga
Choi, Han-Gyu
Shin, Ki-Won
Son, Yeo-Jin
Paik, Tae-Hyun
Kim, Hwa-Jung
author_facet Back, Yong Woo
Choi, Seunga
Choi, Han-Gyu
Shin, Ki-Won
Son, Yeo-Jin
Paik, Tae-Hyun
Kim, Hwa-Jung
author_sort Back, Yong Woo
collection PubMed
description A safe and effective adjuvant is necessary to induce reliable protective efficacy of the protein-based vaccines against tuberculosis (TB). Mycobacterial components, such as synthetic cord factor and arabinogalactan, have been used as one of the adjuvant components. Mycobacterium bovis bacillus Calmette- Guérin cell-wall skeleton (BCG-CWS) has been used as an effective immune-stimulator. However, it is not proven whether BCG-CWS can be an effective adjuvant for the subunit protein vaccine of TB. In this study, we demonstrated that the BCG-CWS effectively coupled with Ag85B and enhanced the conjugated Ag85B activity on the maturation of dendritic cells (DCs). Ag85B-BCG-CWS-matured DCs induced significant Th1 and Th17 responses when compared to BCG-CWS or Ag85B alone. In addition, significant Ag85B-specific Th1 and Th17 responses were induced in Ag85B-BCG-CWS-immunized mice before infection with M. tuberculosis and maintained after infection. Moreover, Ag85B-BCG-CWS showed significant protective effect comparable to live BCG at 6 weeks after infection and maintained its protective efficacy at 32 weeks post-challenge, whereas live BCG did not. These results suggest that the BCG-CWS may be an effective adjuvant candidate for a protein-based vaccine against TB.
format Online
Article
Text
id pubmed-6407753
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-64077532019-03-17 Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses Back, Yong Woo Choi, Seunga Choi, Han-Gyu Shin, Ki-Won Son, Yeo-Jin Paik, Tae-Hyun Kim, Hwa-Jung PLoS One Research Article A safe and effective adjuvant is necessary to induce reliable protective efficacy of the protein-based vaccines against tuberculosis (TB). Mycobacterial components, such as synthetic cord factor and arabinogalactan, have been used as one of the adjuvant components. Mycobacterium bovis bacillus Calmette- Guérin cell-wall skeleton (BCG-CWS) has been used as an effective immune-stimulator. However, it is not proven whether BCG-CWS can be an effective adjuvant for the subunit protein vaccine of TB. In this study, we demonstrated that the BCG-CWS effectively coupled with Ag85B and enhanced the conjugated Ag85B activity on the maturation of dendritic cells (DCs). Ag85B-BCG-CWS-matured DCs induced significant Th1 and Th17 responses when compared to BCG-CWS or Ag85B alone. In addition, significant Ag85B-specific Th1 and Th17 responses were induced in Ag85B-BCG-CWS-immunized mice before infection with M. tuberculosis and maintained after infection. Moreover, Ag85B-BCG-CWS showed significant protective effect comparable to live BCG at 6 weeks after infection and maintained its protective efficacy at 32 weeks post-challenge, whereas live BCG did not. These results suggest that the BCG-CWS may be an effective adjuvant candidate for a protein-based vaccine against TB. Public Library of Science 2019-03-08 /pmc/articles/PMC6407753/ /pubmed/30849108 http://dx.doi.org/10.1371/journal.pone.0213536 Text en © 2019 Back et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Back, Yong Woo
Choi, Seunga
Choi, Han-Gyu
Shin, Ki-Won
Son, Yeo-Jin
Paik, Tae-Hyun
Kim, Hwa-Jung
Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title_full Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title_fullStr Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title_full_unstemmed Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title_short Cell wall skeleton of Mycobacterium bovis BCG enhances the vaccine potential of antigen 85B against tuberculosis by inducing Th1 and Th17 responses
title_sort cell wall skeleton of mycobacterium bovis bcg enhances the vaccine potential of antigen 85b against tuberculosis by inducing th1 and th17 responses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407753/
https://www.ncbi.nlm.nih.gov/pubmed/30849108
http://dx.doi.org/10.1371/journal.pone.0213536
work_keys_str_mv AT backyongwoo cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT choiseunga cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT choihangyu cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT shinkiwon cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT sonyeojin cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT paiktaehyun cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses
AT kimhwajung cellwallskeletonofmycobacteriumbovisbcgenhancesthevaccinepotentialofantigen85bagainsttuberculosisbyinducingth1andth17responses