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Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine
BACKGROUND: DNA vaccines have emerged as an attractive approach for the generation of cytotoxic T lymphocytes (CTL). In our previous study, we found That Toll like receptor (TLR) ligands are promising candidates for the development of novel adjuvants for DNA vaccine. To improve the efficacy of DNA v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727273/ https://www.ncbi.nlm.nih.gov/pubmed/26811064 http://dx.doi.org/10.1186/s12929-016-0238-3 |
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author | Gableh, Fateme Saeidi, Mohsen Hemati, Shaghayegh Hamdi, Kasra Soleimanjahi, Hoorieh Gorji, Ali Ghaemi, Amir |
author_facet | Gableh, Fateme Saeidi, Mohsen Hemati, Shaghayegh Hamdi, Kasra Soleimanjahi, Hoorieh Gorji, Ali Ghaemi, Amir |
author_sort | Gableh, Fateme |
collection | PubMed |
description | BACKGROUND: DNA vaccines have emerged as an attractive approach for the generation of cytotoxic T lymphocytes (CTL). In our previous study, we found That Toll like receptor (TLR) ligands are promising candidates for the development of novel adjuvants for DNA vaccine. To improve the efficacy of DNA vaccine directed against human papillomavirus (HPV) tumors, we evaluated whether co-administration of a TLR4 ligand, monophosphoryl lipid A (MPL), and Natural Killer T Cell Ligand α-Galactosylceramide(α-GalCer) adjuvants with DNA vaccine would influence the anti-tumor efficacy of DNA vaccinations. METHODS: We investigated the effectiveness of α-GalCer and MPL combination as an adjuvant with an HPV-16 E7 DNA vaccine to enhance antitumor immune responses. RESULTS: By using adjuvant combination for a DNA vaccine, we found that the levels of lymphocyte proliferation, CTL activity, IFN- γ, IL-4 and IL-12 responses, and tumor protection against TC-1 cells were significantly increased compared to the DNA vaccine with individual adjuvants. In addition, inhibition of IL-18 signaling during vaccination decreased IFN-γ responses and tumor protection, and that this inhibition suggested stimulatory role of IL-18 in adjuvant effects of α-GalCer and MPL combination. CONCLUSION: The strong adjuvanticity associated with α-GalCer/MPL combination may to be an important tool in the development of novel and strong cancer immunotherapy. |
format | Online Article Text |
id | pubmed-4727273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47272732016-01-27 Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine Gableh, Fateme Saeidi, Mohsen Hemati, Shaghayegh Hamdi, Kasra Soleimanjahi, Hoorieh Gorji, Ali Ghaemi, Amir J Biomed Sci Research BACKGROUND: DNA vaccines have emerged as an attractive approach for the generation of cytotoxic T lymphocytes (CTL). In our previous study, we found That Toll like receptor (TLR) ligands are promising candidates for the development of novel adjuvants for DNA vaccine. To improve the efficacy of DNA vaccine directed against human papillomavirus (HPV) tumors, we evaluated whether co-administration of a TLR4 ligand, monophosphoryl lipid A (MPL), and Natural Killer T Cell Ligand α-Galactosylceramide(α-GalCer) adjuvants with DNA vaccine would influence the anti-tumor efficacy of DNA vaccinations. METHODS: We investigated the effectiveness of α-GalCer and MPL combination as an adjuvant with an HPV-16 E7 DNA vaccine to enhance antitumor immune responses. RESULTS: By using adjuvant combination for a DNA vaccine, we found that the levels of lymphocyte proliferation, CTL activity, IFN- γ, IL-4 and IL-12 responses, and tumor protection against TC-1 cells were significantly increased compared to the DNA vaccine with individual adjuvants. In addition, inhibition of IL-18 signaling during vaccination decreased IFN-γ responses and tumor protection, and that this inhibition suggested stimulatory role of IL-18 in adjuvant effects of α-GalCer and MPL combination. CONCLUSION: The strong adjuvanticity associated with α-GalCer/MPL combination may to be an important tool in the development of novel and strong cancer immunotherapy. BioMed Central 2016-01-25 /pmc/articles/PMC4727273/ /pubmed/26811064 http://dx.doi.org/10.1186/s12929-016-0238-3 Text en © Gableh et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Gableh, Fateme Saeidi, Mohsen Hemati, Shaghayegh Hamdi, Kasra Soleimanjahi, Hoorieh Gorji, Ali Ghaemi, Amir Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title | Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title_full | Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title_fullStr | Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title_full_unstemmed | Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title_short | Combination of the toll like receptor agonist and α-Galactosylceramide as an efficient adjuvant for cancer vaccine |
title_sort | combination of the toll like receptor agonist and α-galactosylceramide as an efficient adjuvant for cancer vaccine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727273/ https://www.ncbi.nlm.nih.gov/pubmed/26811064 http://dx.doi.org/10.1186/s12929-016-0238-3 |
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