Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>

The incidence of infections with nontuberculous mycobacteria (NTM) has been increasing worldwide. The emergence of multidrug-resistant NTM is a serious clinical concern, and a vaccine for NTM has not yet been developed. We previously developed a new recombinant Bacillus Calmette–Guérin (rBCG) vaccin...

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Autores principales: Shihoko Komine-Aizawa, Satoru Mizuno, Kazuhiro Matsuo, Takahiro Namiki, Satoshi Hayakawa, Mitsuo Honda
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:077b4100a78f471f82f3c994dbe021c52021-11-25T19:10:39ZRecombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>10.3390/vaccines91112602076-393Xhttps://doaj.org/article/077b4100a78f471f82f3c994dbe021c52021-11-01T00:00:00Zhttps://www.mdpi.com/2076-393X/9/11/1260https://doaj.org/toc/2076-393XThe incidence of infections with nontuberculous mycobacteria (NTM) has been increasing worldwide. The emergence of multidrug-resistant NTM is a serious clinical concern, and a vaccine for NTM has not yet been developed. We previously developed a new recombinant Bacillus Calmette–Guérin (rBCG) vaccine encoding the antigen 85B (Ag85B) protein of <i>Mycobacterium kansasii</i>—termed rBCG-Mkan85B—which was used together with a booster immunization with plasmid DNA expressing the same <i>M. kansasii</i> Ag85B gene (DNA-Mkan85B). We reported that rBCG-Mkan85B/DNA-Mkan85B prime–boost immunization elicited various NTM strain-specific CD4<sup>+</sup> and CD8<sup>+</sup> T cells and induced <i>Mycobacterium</i> <i>tuberculosis</i>-specific immunity. In this study, to investigate the protective effect against <i>M. kansasii</i> infection, we challenged mice vaccinated with a rBCG-Mkan85B or rBCG-Mkan85B/DNA-Mkan85B prime–boost strategy with virulent <i>M. kansasii</i>. Although BCG and rBCG-Mkan85B immunization each suppressed the growth of <i>M. kansasii</i> in the mouse lungs, the rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination reduced the bacterial burden more significantly. Moreover, the rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination induced antigen-specific CD4<sup>+</sup> and CD8<sup>+</sup> T cells. Our data suggest that rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination effectively enhances antigen-specific T cells. Our novel rBCG could be a potential alternative to clinical BCG for preventing various NTM infections.Shihoko Komine-AizawaSatoru MizunoKazuhiro MatsuoTakahiro NamikiSatoshi HayakawaMitsuo HondaMDPI AGarticle<i>Mycobacterium kansasii</i>CD8<sup>+</sup> T CellsCD4<sup>+</sup> T Cellsrecombinant BCGMedicineRENVaccines, Vol 9, Iss 1260, p 1260 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>Mycobacterium kansasii</i>
CD8<sup>+</sup> T Cells
CD4<sup>+</sup> T Cells
recombinant BCG
Medicine
R
spellingShingle <i>Mycobacterium kansasii</i>
CD8<sup>+</sup> T Cells
CD4<sup>+</sup> T Cells
recombinant BCG
Medicine
R
Shihoko Komine-Aizawa
Satoru Mizuno
Kazuhiro Matsuo
Takahiro Namiki
Satoshi Hayakawa
Mitsuo Honda
Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
description The incidence of infections with nontuberculous mycobacteria (NTM) has been increasing worldwide. The emergence of multidrug-resistant NTM is a serious clinical concern, and a vaccine for NTM has not yet been developed. We previously developed a new recombinant Bacillus Calmette–Guérin (rBCG) vaccine encoding the antigen 85B (Ag85B) protein of <i>Mycobacterium kansasii</i>—termed rBCG-Mkan85B—which was used together with a booster immunization with plasmid DNA expressing the same <i>M. kansasii</i> Ag85B gene (DNA-Mkan85B). We reported that rBCG-Mkan85B/DNA-Mkan85B prime–boost immunization elicited various NTM strain-specific CD4<sup>+</sup> and CD8<sup>+</sup> T cells and induced <i>Mycobacterium</i> <i>tuberculosis</i>-specific immunity. In this study, to investigate the protective effect against <i>M. kansasii</i> infection, we challenged mice vaccinated with a rBCG-Mkan85B or rBCG-Mkan85B/DNA-Mkan85B prime–boost strategy with virulent <i>M. kansasii</i>. Although BCG and rBCG-Mkan85B immunization each suppressed the growth of <i>M. kansasii</i> in the mouse lungs, the rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination reduced the bacterial burden more significantly. Moreover, the rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination induced antigen-specific CD4<sup>+</sup> and CD8<sup>+</sup> T cells. Our data suggest that rBCG-Mkan85B/DNA-Mkan85B prime–boost vaccination effectively enhances antigen-specific T cells. Our novel rBCG could be a potential alternative to clinical BCG for preventing various NTM infections.
format article
author Shihoko Komine-Aizawa
Satoru Mizuno
Kazuhiro Matsuo
Takahiro Namiki
Satoshi Hayakawa
Mitsuo Honda
author_facet Shihoko Komine-Aizawa
Satoru Mizuno
Kazuhiro Matsuo
Takahiro Namiki
Satoshi Hayakawa
Mitsuo Honda
author_sort Shihoko Komine-Aizawa
title Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
title_short Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
title_full Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
title_fullStr Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
title_full_unstemmed Recombinant BCG-Prime and DNA-Boost Immunization Confers Mice with Enhanced Protection against <i>Mycobacterium kansasii</i>
title_sort recombinant bcg-prime and dna-boost immunization confers mice with enhanced protection against <i>mycobacterium kansasii</i>
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/077b4100a78f471f82f3c994dbe021c5
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