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Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes

Chemically modified mRNA is an efficient, biocompatible modality for therapeutic protein expression. We report a first-time-in-human study of this modality, aiming to evaluate safety and potential therapeutic effects. Men with type 2 diabetes mellitus (T2DM) received intradermal injections of modifi...

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Autores principales: Gan, Li-Ming, Lagerström-Fermér, Maria, Carlsson, Leif G., Arfvidsson, Cecilia, Egnell, Ann-Charlotte, Rudvik, Anna, Kjaer, Magnus, Collén, Anna, Thompson, James D., Joyal, John, Chialda, Ligia, Koernicke, Thomas, Fuhr, Rainard, Chien, Kenneth R., Fritsche-Danielson, Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382754/
https://www.ncbi.nlm.nih.gov/pubmed/30787295
http://dx.doi.org/10.1038/s41467-019-08852-4
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author Gan, Li-Ming
Lagerström-Fermér, Maria
Carlsson, Leif G.
Arfvidsson, Cecilia
Egnell, Ann-Charlotte
Rudvik, Anna
Kjaer, Magnus
Collén, Anna
Thompson, James D.
Joyal, John
Chialda, Ligia
Koernicke, Thomas
Fuhr, Rainard
Chien, Kenneth R.
Fritsche-Danielson, Regina
author_facet Gan, Li-Ming
Lagerström-Fermér, Maria
Carlsson, Leif G.
Arfvidsson, Cecilia
Egnell, Ann-Charlotte
Rudvik, Anna
Kjaer, Magnus
Collén, Anna
Thompson, James D.
Joyal, John
Chialda, Ligia
Koernicke, Thomas
Fuhr, Rainard
Chien, Kenneth R.
Fritsche-Danielson, Regina
author_sort Gan, Li-Ming
collection PubMed
description Chemically modified mRNA is an efficient, biocompatible modality for therapeutic protein expression. We report a first-time-in-human study of this modality, aiming to evaluate safety and potential therapeutic effects. Men with type 2 diabetes mellitus (T2DM) received intradermal injections of modified mRNA encoding vascular endothelial growth factor A (VEGF-A) or buffered saline placebo (ethical obligations precluded use of a non-translatable mRNA control) at randomized sites on the forearm. The only causally treatment-related adverse events were mild injection-site reactions. Skin microdialysis revealed elevated VEGF-A protein levels at mRNA-treated sites versus placebo-treated sites from about 4–24 hours post-administration. Enhancements in basal skin blood flow at 4 hours and 7 days post-administration were detected using laser Doppler fluximetry and imaging. Intradermal VEGF-A mRNA was well tolerated and led to local functional VEGF-A protein expression and transient skin blood flow enhancement in men with T2DM. VEGF-A mRNA may have therapeutic potential for regenerative angiogenesis.
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spelling pubmed-63827542019-02-22 Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes Gan, Li-Ming Lagerström-Fermér, Maria Carlsson, Leif G. Arfvidsson, Cecilia Egnell, Ann-Charlotte Rudvik, Anna Kjaer, Magnus Collén, Anna Thompson, James D. Joyal, John Chialda, Ligia Koernicke, Thomas Fuhr, Rainard Chien, Kenneth R. Fritsche-Danielson, Regina Nat Commun Article Chemically modified mRNA is an efficient, biocompatible modality for therapeutic protein expression. We report a first-time-in-human study of this modality, aiming to evaluate safety and potential therapeutic effects. Men with type 2 diabetes mellitus (T2DM) received intradermal injections of modified mRNA encoding vascular endothelial growth factor A (VEGF-A) or buffered saline placebo (ethical obligations precluded use of a non-translatable mRNA control) at randomized sites on the forearm. The only causally treatment-related adverse events were mild injection-site reactions. Skin microdialysis revealed elevated VEGF-A protein levels at mRNA-treated sites versus placebo-treated sites from about 4–24 hours post-administration. Enhancements in basal skin blood flow at 4 hours and 7 days post-administration were detected using laser Doppler fluximetry and imaging. Intradermal VEGF-A mRNA was well tolerated and led to local functional VEGF-A protein expression and transient skin blood flow enhancement in men with T2DM. VEGF-A mRNA may have therapeutic potential for regenerative angiogenesis. Nature Publishing Group UK 2019-02-20 /pmc/articles/PMC6382754/ /pubmed/30787295 http://dx.doi.org/10.1038/s41467-019-08852-4 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gan, Li-Ming
Lagerström-Fermér, Maria
Carlsson, Leif G.
Arfvidsson, Cecilia
Egnell, Ann-Charlotte
Rudvik, Anna
Kjaer, Magnus
Collén, Anna
Thompson, James D.
Joyal, John
Chialda, Ligia
Koernicke, Thomas
Fuhr, Rainard
Chien, Kenneth R.
Fritsche-Danielson, Regina
Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title_full Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title_fullStr Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title_full_unstemmed Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title_short Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
title_sort intradermal delivery of modified mrna encoding vegf-a in patients with type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382754/
https://www.ncbi.nlm.nih.gov/pubmed/30787295
http://dx.doi.org/10.1038/s41467-019-08852-4
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