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Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions

Therapeutic mRNA delivery has been described for several treatment options, such as vaccination and cancer immunotherapy. However, mRNA delivery has to be accompanied by the development and testing of suitable carrier materials due to the instability of mRNAs in human body fluids. In the present stu...

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Autores principales: Jansig, Edith, Geissler, Stefanie, Rieckmann, Vera, Kuenemund, Anja, Hietel, Benjamin, Schenk, Mathias, Wussow, Sebastian, Kreideweiss, Patrick, Panzner, Steffen, Reinsch, Christian, Cynis, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494895/
https://www.ncbi.nlm.nih.gov/pubmed/32934311
http://dx.doi.org/10.1038/s41598-020-72004-8
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author Jansig, Edith
Geissler, Stefanie
Rieckmann, Vera
Kuenemund, Anja
Hietel, Benjamin
Schenk, Mathias
Wussow, Sebastian
Kreideweiss, Patrick
Panzner, Steffen
Reinsch, Christian
Cynis, Holger
author_facet Jansig, Edith
Geissler, Stefanie
Rieckmann, Vera
Kuenemund, Anja
Hietel, Benjamin
Schenk, Mathias
Wussow, Sebastian
Kreideweiss, Patrick
Panzner, Steffen
Reinsch, Christian
Cynis, Holger
author_sort Jansig, Edith
collection PubMed
description Therapeutic mRNA delivery has been described for several treatment options, such as vaccination and cancer immunotherapy. However, mRNA delivery has to be accompanied by the development and testing of suitable carrier materials due to the instability of mRNAs in human body fluids. In the present study, we investigated the ability of recently developed Viromers to deliver mRNAs in a classical inflammatory setting. We tested mRNAs coding for active components of preclinical (7ND) and approved (sTNF-RII) biologics, in vitro and in vivo. 7ND is an established blocker of the CCR2 axis, whereas sTNF-RII is the active component of the approved drug Etanercept. Viromer/mRNA complexes were transfected into murine macrophages in vitro. Protein expression was analysed using Luciferase reporter expression and mainly identified in spleen, blood and bone marrow in vivo. 7ND-mRNA delivery led to efficient blockage of monocytes infiltration in thioglycolate-induced peritonitis in mice, underlining the ability of Viromers to deliver a therapeutic mRNA cargo without overt toxicity. Therefore, we propose Viromer-based mRNA delivery as a suitable option for the treatment of inflammatory disorders beyond infusion of biological molecules.
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spelling pubmed-74948952020-09-18 Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions Jansig, Edith Geissler, Stefanie Rieckmann, Vera Kuenemund, Anja Hietel, Benjamin Schenk, Mathias Wussow, Sebastian Kreideweiss, Patrick Panzner, Steffen Reinsch, Christian Cynis, Holger Sci Rep Article Therapeutic mRNA delivery has been described for several treatment options, such as vaccination and cancer immunotherapy. However, mRNA delivery has to be accompanied by the development and testing of suitable carrier materials due to the instability of mRNAs in human body fluids. In the present study, we investigated the ability of recently developed Viromers to deliver mRNAs in a classical inflammatory setting. We tested mRNAs coding for active components of preclinical (7ND) and approved (sTNF-RII) biologics, in vitro and in vivo. 7ND is an established blocker of the CCR2 axis, whereas sTNF-RII is the active component of the approved drug Etanercept. Viromer/mRNA complexes were transfected into murine macrophages in vitro. Protein expression was analysed using Luciferase reporter expression and mainly identified in spleen, blood and bone marrow in vivo. 7ND-mRNA delivery led to efficient blockage of monocytes infiltration in thioglycolate-induced peritonitis in mice, underlining the ability of Viromers to deliver a therapeutic mRNA cargo without overt toxicity. Therefore, we propose Viromer-based mRNA delivery as a suitable option for the treatment of inflammatory disorders beyond infusion of biological molecules. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7494895/ /pubmed/32934311 http://dx.doi.org/10.1038/s41598-020-72004-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jansig, Edith
Geissler, Stefanie
Rieckmann, Vera
Kuenemund, Anja
Hietel, Benjamin
Schenk, Mathias
Wussow, Sebastian
Kreideweiss, Patrick
Panzner, Steffen
Reinsch, Christian
Cynis, Holger
Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title_full Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title_fullStr Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title_full_unstemmed Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title_short Viromers as carriers for mRNA-mediated expression of therapeutic molecules under inflammatory conditions
title_sort viromers as carriers for mrna-mediated expression of therapeutic molecules under inflammatory conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494895/
https://www.ncbi.nlm.nih.gov/pubmed/32934311
http://dx.doi.org/10.1038/s41598-020-72004-8
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