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Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin
In this work, we studied the expression kinetics and innate immune response of a self-amplifying mRNA (sa-RNA) after electroporation and lipid-nanoparticle (LNP)-mediated delivery in the skin of mice. Intradermal electroporation of the sa-RNA resulted in a plateau-shaped expression, with the plateau...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722285/ https://www.ncbi.nlm.nih.gov/pubmed/31472371 http://dx.doi.org/10.1016/j.omtn.2019.08.001 |
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author | Huysmans, Hanne Zhong, Zifu De Temmerman, Joyca Mui, Barbara L. Tam, Ying K. Mc Cafferty, Séan Gitsels, Arlieke Vanrompay, Daisy Sanders, Niek N. |
author_facet | Huysmans, Hanne Zhong, Zifu De Temmerman, Joyca Mui, Barbara L. Tam, Ying K. Mc Cafferty, Séan Gitsels, Arlieke Vanrompay, Daisy Sanders, Niek N. |
author_sort | Huysmans, Hanne |
collection | PubMed |
description | In this work, we studied the expression kinetics and innate immune response of a self-amplifying mRNA (sa-RNA) after electroporation and lipid-nanoparticle (LNP)-mediated delivery in the skin of mice. Intradermal electroporation of the sa-RNA resulted in a plateau-shaped expression, with the plateau between day 3 and day 10. The overall protein expression of sa-RNA was significantly higher than that obtained after electroporation of plasmid DNA (pDNA) or non-replication mRNAs. Moreover, using IFN-β reporter mice, we elucidated that intradermal electroporation of sa-RNA induced a short-lived moderate innate immune response, which did not affect the expression of the sa-RNA. A completely different expression profile and innate immune response were observed when LNPs were used. The expression peaked 24 h after intradermal injection of sa-RNA-LNPs and subsequently showed a sharp drop. This drop might be explained by a translational blockage caused by the strong innate immune response that we observed in IFN-β reporter mice shortly (4 h) after intradermal injection of sa-RNA-LNPs. A final interesting observation was the capacity of sa-RNA-LNPs to transfect the draining lymph nodes after intradermal injection. |
format | Online Article Text |
id | pubmed-6722285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-67222852019-09-10 Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin Huysmans, Hanne Zhong, Zifu De Temmerman, Joyca Mui, Barbara L. Tam, Ying K. Mc Cafferty, Séan Gitsels, Arlieke Vanrompay, Daisy Sanders, Niek N. Mol Ther Nucleic Acids Article In this work, we studied the expression kinetics and innate immune response of a self-amplifying mRNA (sa-RNA) after electroporation and lipid-nanoparticle (LNP)-mediated delivery in the skin of mice. Intradermal electroporation of the sa-RNA resulted in a plateau-shaped expression, with the plateau between day 3 and day 10. The overall protein expression of sa-RNA was significantly higher than that obtained after electroporation of plasmid DNA (pDNA) or non-replication mRNAs. Moreover, using IFN-β reporter mice, we elucidated that intradermal electroporation of sa-RNA induced a short-lived moderate innate immune response, which did not affect the expression of the sa-RNA. A completely different expression profile and innate immune response were observed when LNPs were used. The expression peaked 24 h after intradermal injection of sa-RNA-LNPs and subsequently showed a sharp drop. This drop might be explained by a translational blockage caused by the strong innate immune response that we observed in IFN-β reporter mice shortly (4 h) after intradermal injection of sa-RNA-LNPs. A final interesting observation was the capacity of sa-RNA-LNPs to transfect the draining lymph nodes after intradermal injection. American Society of Gene & Cell Therapy 2019-08-07 /pmc/articles/PMC6722285/ /pubmed/31472371 http://dx.doi.org/10.1016/j.omtn.2019.08.001 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Huysmans, Hanne Zhong, Zifu De Temmerman, Joyca Mui, Barbara L. Tam, Ying K. Mc Cafferty, Séan Gitsels, Arlieke Vanrompay, Daisy Sanders, Niek N. Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title | Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title_full | Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title_fullStr | Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title_full_unstemmed | Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title_short | Expression Kinetics and Innate Immune Response after Electroporation and LNP-Mediated Delivery of a Self-Amplifying mRNA in the Skin |
title_sort | expression kinetics and innate immune response after electroporation and lnp-mediated delivery of a self-amplifying mrna in the skin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722285/ https://www.ncbi.nlm.nih.gov/pubmed/31472371 http://dx.doi.org/10.1016/j.omtn.2019.08.001 |
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