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Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma
Antigen peptides and adjuvants have been extensively investigated for cancer immunotherapy, and they are expected to elicit specific immune responses for cancer treatment. However, the anti-cancer efficacy of antigen peptide and adjuvant-based cancer vaccines has been limited due to the inefficient...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539931/ https://www.ncbi.nlm.nih.gov/pubmed/31060324 http://dx.doi.org/10.3390/ijms20092207 |
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author | Mu, Li-Min Liu, Lei Liu, Rui Du, Ya-Fei Luo, Qian Xu, Jia-Rui Xie, Ying Lu, Wan-Liang |
author_facet | Mu, Li-Min Liu, Lei Liu, Rui Du, Ya-Fei Luo, Qian Xu, Jia-Rui Xie, Ying Lu, Wan-Liang |
author_sort | Mu, Li-Min |
collection | PubMed |
description | Antigen peptides and adjuvants have been extensively investigated for cancer immunotherapy, and they are expected to elicit specific immune responses for cancer treatment. However, the anti-cancer efficacy of antigen peptide and adjuvant-based cancer vaccines has been limited due to the inefficient delivery to draining lymph nodes after administration. Therefore, it is necessary to develop a suitable delivery system to transport antigen peptides and adjuvants. Here, we report a novel type of nanostructured lipovaccines for the treatment of melanoma by delivering antigen peptide (SL9) and oligodeoxynucleotide adjuvant (CpG) to the lymphatic vessels and to the draining lymph node. The SL9-CpG lipovaccines were characterized using dynamic laser scattering (DLS) and transmission electron microscopy (TEM). The lymph uptake, immune response elicitation and treatment effects were evaluated on melanoma-bearing C57BL/6 mice using flow cytometry (FCM), enzyme-linked immunosorbent assay (ELISA) and tumor inhibitory efficacy. The SL9-CpG lipovaccines were uniform with a nanoscale size (~70 nm), had high encapsulation efficiency, and exhibited effective lymph uptake, resulting in activation of specific cytotoxic CD8+ T cells, and release of IFN-γ, and a robust inhibition of tumor growth. Therefore, the nanostructured SL9-CpG lipovaccines offer a promising strategy for melanoma treatment. |
format | Online Article Text |
id | pubmed-6539931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65399312019-06-04 Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma Mu, Li-Min Liu, Lei Liu, Rui Du, Ya-Fei Luo, Qian Xu, Jia-Rui Xie, Ying Lu, Wan-Liang Int J Mol Sci Article Antigen peptides and adjuvants have been extensively investigated for cancer immunotherapy, and they are expected to elicit specific immune responses for cancer treatment. However, the anti-cancer efficacy of antigen peptide and adjuvant-based cancer vaccines has been limited due to the inefficient delivery to draining lymph nodes after administration. Therefore, it is necessary to develop a suitable delivery system to transport antigen peptides and adjuvants. Here, we report a novel type of nanostructured lipovaccines for the treatment of melanoma by delivering antigen peptide (SL9) and oligodeoxynucleotide adjuvant (CpG) to the lymphatic vessels and to the draining lymph node. The SL9-CpG lipovaccines were characterized using dynamic laser scattering (DLS) and transmission electron microscopy (TEM). The lymph uptake, immune response elicitation and treatment effects were evaluated on melanoma-bearing C57BL/6 mice using flow cytometry (FCM), enzyme-linked immunosorbent assay (ELISA) and tumor inhibitory efficacy. The SL9-CpG lipovaccines were uniform with a nanoscale size (~70 nm), had high encapsulation efficiency, and exhibited effective lymph uptake, resulting in activation of specific cytotoxic CD8+ T cells, and release of IFN-γ, and a robust inhibition of tumor growth. Therefore, the nanostructured SL9-CpG lipovaccines offer a promising strategy for melanoma treatment. MDPI 2019-05-05 /pmc/articles/PMC6539931/ /pubmed/31060324 http://dx.doi.org/10.3390/ijms20092207 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mu, Li-Min Liu, Lei Liu, Rui Du, Ya-Fei Luo, Qian Xu, Jia-Rui Xie, Ying Lu, Wan-Liang Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title | Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title_full | Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title_fullStr | Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title_full_unstemmed | Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title_short | Nanostructured SL9-CpG Lipovaccines Elicit Immune Response for the Treatment of Melanoma |
title_sort | nanostructured sl9-cpg lipovaccines elicit immune response for the treatment of melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539931/ https://www.ncbi.nlm.nih.gov/pubmed/31060324 http://dx.doi.org/10.3390/ijms20092207 |
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