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Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice
Background: Various vaccine adjuvants have been developed to eliminate HBV from patients with chronic HBV infection. In addition, spermidine (SPD), a type of polyamine, has been reported to enhance the activity of immune cells. In the present study, we investigated whether the combination of SPD and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043579/ https://www.ncbi.nlm.nih.gov/pubmed/36972390 http://dx.doi.org/10.1097/HC9.0000000000000104 |
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author | Ito, Daisuke Ito, Hiroyasu Ando, Tatsuya Sakai, Yasuhiro Ideta, Takayasu Ishii, Ken J. Ishikawa, Tetsuya Shimizu, Masahito |
author_facet | Ito, Daisuke Ito, Hiroyasu Ando, Tatsuya Sakai, Yasuhiro Ideta, Takayasu Ishii, Ken J. Ishikawa, Tetsuya Shimizu, Masahito |
author_sort | Ito, Daisuke |
collection | PubMed |
description | Background: Various vaccine adjuvants have been developed to eliminate HBV from patients with chronic HBV infection. In addition, spermidine (SPD), a type of polyamine, has been reported to enhance the activity of immune cells. In the present study, we investigated whether the combination of SPD and vaccine adjuvant enhances the HBV antigen-specific immune response to HBV vaccination. Methods: Wild-type and HBV-transgenic (HBV-Tg) mice were vaccinated 2 or 3 times. SPD was orally administered in drinking water. Cyclic guanosine monophosphate–AMP (cGAMP) and nanoparticulate CpG-ODN (K3-SPG) were used as the HBV vaccine adjuvants. The HBV antigen-specific immune response was evaluated by measuring the HBsAb titer in blood collected over time and the number of interferon-γ producing cells by enzyme-linked immunospot assay. Results: The administration of HBsAg + cGAMP + SPD or HBsAg + K3-SPG + SPD significantly enhanced HBsAg-specific interferon-γ production by CD8 T cells from wild-type and HBV-Tg mice. The administration of HBsAg, cGAMP, and SPD increased serum HBsAb levels in wild-type and HBV-Tg mice. In HBV-Tg mice, the administration of SPD + cGAMP or SPD + K3-SPG with HBV vaccination significantly reduced HBsAg levels in the liver and serum. CONCLUSIONS: These results indicate that the combination of HBV vaccine adjuvant and SPD induces a stronger humoral and cellular immune response through T-cell activation. These treatments may support the development of a strategy to completely eliminate HBV. |
format | Online Article Text |
id | pubmed-10043579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-100435792023-03-29 Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice Ito, Daisuke Ito, Hiroyasu Ando, Tatsuya Sakai, Yasuhiro Ideta, Takayasu Ishii, Ken J. Ishikawa, Tetsuya Shimizu, Masahito Hepatol Commun Original Article Background: Various vaccine adjuvants have been developed to eliminate HBV from patients with chronic HBV infection. In addition, spermidine (SPD), a type of polyamine, has been reported to enhance the activity of immune cells. In the present study, we investigated whether the combination of SPD and vaccine adjuvant enhances the HBV antigen-specific immune response to HBV vaccination. Methods: Wild-type and HBV-transgenic (HBV-Tg) mice were vaccinated 2 or 3 times. SPD was orally administered in drinking water. Cyclic guanosine monophosphate–AMP (cGAMP) and nanoparticulate CpG-ODN (K3-SPG) were used as the HBV vaccine adjuvants. The HBV antigen-specific immune response was evaluated by measuring the HBsAb titer in blood collected over time and the number of interferon-γ producing cells by enzyme-linked immunospot assay. Results: The administration of HBsAg + cGAMP + SPD or HBsAg + K3-SPG + SPD significantly enhanced HBsAg-specific interferon-γ production by CD8 T cells from wild-type and HBV-Tg mice. The administration of HBsAg, cGAMP, and SPD increased serum HBsAb levels in wild-type and HBV-Tg mice. In HBV-Tg mice, the administration of SPD + cGAMP or SPD + K3-SPG with HBV vaccination significantly reduced HBsAg levels in the liver and serum. CONCLUSIONS: These results indicate that the combination of HBV vaccine adjuvant and SPD induces a stronger humoral and cellular immune response through T-cell activation. These treatments may support the development of a strategy to completely eliminate HBV. Lippincott Williams & Wilkins 2023-03-24 /pmc/articles/PMC10043579/ /pubmed/36972390 http://dx.doi.org/10.1097/HC9.0000000000000104 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/) (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Original Article Ito, Daisuke Ito, Hiroyasu Ando, Tatsuya Sakai, Yasuhiro Ideta, Takayasu Ishii, Ken J. Ishikawa, Tetsuya Shimizu, Masahito Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title | Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title_full | Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title_fullStr | Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title_full_unstemmed | Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title_short | Spermidine enhances the efficacy of adjuvant in HBV vaccination in mice |
title_sort | spermidine enhances the efficacy of adjuvant in hbv vaccination in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043579/ https://www.ncbi.nlm.nih.gov/pubmed/36972390 http://dx.doi.org/10.1097/HC9.0000000000000104 |
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