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Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers

Omiganan (OMN; a synthetic cationic peptide) and imiquimod (IMQ; a TLR7 agonist) have synergistic effects on interferon responses in vitro. The objective of this study was to translate this to a human model for proof‐of‐concept, and to explore the potential of OMN add‐on treatment for viral skin dis...

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Autores principales: Niemeyer‐van der Kolk, Tessa, Assil, Salma, Buters, Thomas P., Rijsbergen, Melanie, Klaassen, Erica S., Feiss, Gary, Florencia, Edwin, Prens, Errol P., Burggraaf, Jacobus, van Doorn, Martijn B.A., Rissmann, Robert, Moerland, Matthijs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214655/
https://www.ncbi.nlm.nih.gov/pubmed/32043302
http://dx.doi.org/10.1111/cts.12741
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author Niemeyer‐van der Kolk, Tessa
Assil, Salma
Buters, Thomas P.
Rijsbergen, Melanie
Klaassen, Erica S.
Feiss, Gary
Florencia, Edwin
Prens, Errol P.
Burggraaf, Jacobus
van Doorn, Martijn B.A.
Rissmann, Robert
Moerland, Matthijs
author_facet Niemeyer‐van der Kolk, Tessa
Assil, Salma
Buters, Thomas P.
Rijsbergen, Melanie
Klaassen, Erica S.
Feiss, Gary
Florencia, Edwin
Prens, Errol P.
Burggraaf, Jacobus
van Doorn, Martijn B.A.
Rissmann, Robert
Moerland, Matthijs
author_sort Niemeyer‐van der Kolk, Tessa
collection PubMed
description Omiganan (OMN; a synthetic cationic peptide) and imiquimod (IMQ; a TLR7 agonist) have synergistic effects on interferon responses in vitro. The objective of this study was to translate this to a human model for proof‐of‐concept, and to explore the potential of OMN add‐on treatment for viral skin diseases. Sixteen healthy volunteers received topical IMQ, OMN, or a combination of both for up to 4 days on tape‐stripped skin. Skin inflammation was quantified by laser speckle contrast imaging and 2D photography, and molecular and cellular responses were analyzed in biopsies. IMQ treatment induced an inflammatory response of the skin. Co‐treatment with OMN enhanced this inflammatory response to IMQ, with increases in perfusion (+17.1%; 95% confidence interval (CI) 5.6%–30%; P < 0.01) and erythema (+1.5; 95% CI 0.25%–2.83; P = 0.02). Interferon regulatory factor‐driven and NFκB‐driven responses following TLR7 stimulation were enhanced by OMN (increases in IL‐6, IL‐10, MXA, and IFNɣ), and more immune cell infiltration was observed (in particular CD4+, CD8+, and CD14+ cells). These findings are in line with the earlier mechanistic in vitro data, and support evaluation of imiquimod/OMN combination therapy in human papillomavirus‐induced skin diseases.
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spelling pubmed-72146552020-05-13 Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers Niemeyer‐van der Kolk, Tessa Assil, Salma Buters, Thomas P. Rijsbergen, Melanie Klaassen, Erica S. Feiss, Gary Florencia, Edwin Prens, Errol P. Burggraaf, Jacobus van Doorn, Martijn B.A. Rissmann, Robert Moerland, Matthijs Clin Transl Sci Research Omiganan (OMN; a synthetic cationic peptide) and imiquimod (IMQ; a TLR7 agonist) have synergistic effects on interferon responses in vitro. The objective of this study was to translate this to a human model for proof‐of‐concept, and to explore the potential of OMN add‐on treatment for viral skin diseases. Sixteen healthy volunteers received topical IMQ, OMN, or a combination of both for up to 4 days on tape‐stripped skin. Skin inflammation was quantified by laser speckle contrast imaging and 2D photography, and molecular and cellular responses were analyzed in biopsies. IMQ treatment induced an inflammatory response of the skin. Co‐treatment with OMN enhanced this inflammatory response to IMQ, with increases in perfusion (+17.1%; 95% confidence interval (CI) 5.6%–30%; P < 0.01) and erythema (+1.5; 95% CI 0.25%–2.83; P = 0.02). Interferon regulatory factor‐driven and NFκB‐driven responses following TLR7 stimulation were enhanced by OMN (increases in IL‐6, IL‐10, MXA, and IFNɣ), and more immune cell infiltration was observed (in particular CD4+, CD8+, and CD14+ cells). These findings are in line with the earlier mechanistic in vitro data, and support evaluation of imiquimod/OMN combination therapy in human papillomavirus‐induced skin diseases. John Wiley and Sons Inc. 2020-02-13 2020-05 /pmc/articles/PMC7214655/ /pubmed/32043302 http://dx.doi.org/10.1111/cts.12741 Text en © 2020 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Niemeyer‐van der Kolk, Tessa
Assil, Salma
Buters, Thomas P.
Rijsbergen, Melanie
Klaassen, Erica S.
Feiss, Gary
Florencia, Edwin
Prens, Errol P.
Burggraaf, Jacobus
van Doorn, Martijn B.A.
Rissmann, Robert
Moerland, Matthijs
Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title_full Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title_fullStr Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title_full_unstemmed Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title_short Omiganan Enhances Imiquimod‐Induced Inflammatory Responses in Skin of Healthy Volunteers
title_sort omiganan enhances imiquimod‐induced inflammatory responses in skin of healthy volunteers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214655/
https://www.ncbi.nlm.nih.gov/pubmed/32043302
http://dx.doi.org/10.1111/cts.12741
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