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Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?

Background: SARS-Cov2 has raised concerns among dermatologists regarding psoriasis and its respective treatments. Comorbidities, which induce the expression of the proprotease furin have been associated with severe course of COVID-19. Furin and angiotensin converting enzyme 2 (ACE2) play a major rol...

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Autores principales: Graier, Thomas, Golob-Schwarzl, Nicole, Weger, Wolfgang, Benezeder, Theresa, Painsi, Clemens, Salmhofer, Wolfgang, Wolf, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902756/
https://www.ncbi.nlm.nih.gov/pubmed/33644099
http://dx.doi.org/10.3389/fmed.2021.624462
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author Graier, Thomas
Golob-Schwarzl, Nicole
Weger, Wolfgang
Benezeder, Theresa
Painsi, Clemens
Salmhofer, Wolfgang
Wolf, Peter
author_facet Graier, Thomas
Golob-Schwarzl, Nicole
Weger, Wolfgang
Benezeder, Theresa
Painsi, Clemens
Salmhofer, Wolfgang
Wolf, Peter
author_sort Graier, Thomas
collection PubMed
description Background: SARS-Cov2 has raised concerns among dermatologists regarding psoriasis and its respective treatments. Comorbidities, which induce the expression of the proprotease furin have been associated with severe course of COVID-19. Furin and angiotensin converting enzyme 2 (ACE2) play a major role in viral host cell entry of SARS-Cov2. Objective: To evaluate mRNA expression of Furin and ACE2 from blood cells in psoriasis patients, and whether systemic or topical treatment reduces expression levels. Methods: This observational translational study analyzed blood samples from patients from a clinical trial and samples retrieved from the biobank of the Psoriasis Registry Austria (PsoRA). Furin and ACE2 expression levels were analyzed prior to as well as 3 and 12–24 months after start of biologic treatment with either ustekinumab or secukinumab. Additionally, the study analyzed expression levels prior to, 6 days after start of dithranol treatment and 4–6 weeks after end of dithranol treatment. Results: Furin mRNA expression was significantly increased at baseline in the biologic (4.9 ± 2.6 fold, p < 0.0001) and in the dithranol group (2.7 ± 1.4 fold, p < 0.001) compared to controls. There was a trend for arthritis patients to express more furin than patients with psoriatic skin involvement only (5.26 ± 2.30 vs. 3.48 ± 2.27, p = 0.078). Analyzing furin mRNA expression after treatment initiation with secukinumab or ustekinumab revealed a normalization of levels after 3 and 12 to 24 months. Similar findings were obtained for patients treated with dithranol, with significantly decreased expression levels 6 days after start of dithranol treatment and also at follow-up, (4–6 weeks after dithranol treatment had been terminated). ACE2 expression levels did not differ from controls at any timepoint, regardless of biologic or topical treatment. Conclusion: Significantly overexpressed levels of furin were observed in untreated patients, and, thus, these patients may be at risk for infection and a severe course of COVID-19. However, the data indicate that successful therapeutic intervention in psoriasis, by systemic biologic or topical treatment, can efficiently reduce furin levels in blood cells, possibly limiting the risk of psoriasis patients for a severe COVID-19 course. Clinical Trial Registration: ClinicalTrials.gov, identifier NCT02752672.
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spelling pubmed-79027562021-02-25 Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2? Graier, Thomas Golob-Schwarzl, Nicole Weger, Wolfgang Benezeder, Theresa Painsi, Clemens Salmhofer, Wolfgang Wolf, Peter Front Med (Lausanne) Medicine Background: SARS-Cov2 has raised concerns among dermatologists regarding psoriasis and its respective treatments. Comorbidities, which induce the expression of the proprotease furin have been associated with severe course of COVID-19. Furin and angiotensin converting enzyme 2 (ACE2) play a major role in viral host cell entry of SARS-Cov2. Objective: To evaluate mRNA expression of Furin and ACE2 from blood cells in psoriasis patients, and whether systemic or topical treatment reduces expression levels. Methods: This observational translational study analyzed blood samples from patients from a clinical trial and samples retrieved from the biobank of the Psoriasis Registry Austria (PsoRA). Furin and ACE2 expression levels were analyzed prior to as well as 3 and 12–24 months after start of biologic treatment with either ustekinumab or secukinumab. Additionally, the study analyzed expression levels prior to, 6 days after start of dithranol treatment and 4–6 weeks after end of dithranol treatment. Results: Furin mRNA expression was significantly increased at baseline in the biologic (4.9 ± 2.6 fold, p < 0.0001) and in the dithranol group (2.7 ± 1.4 fold, p < 0.001) compared to controls. There was a trend for arthritis patients to express more furin than patients with psoriatic skin involvement only (5.26 ± 2.30 vs. 3.48 ± 2.27, p = 0.078). Analyzing furin mRNA expression after treatment initiation with secukinumab or ustekinumab revealed a normalization of levels after 3 and 12 to 24 months. Similar findings were obtained for patients treated with dithranol, with significantly decreased expression levels 6 days after start of dithranol treatment and also at follow-up, (4–6 weeks after dithranol treatment had been terminated). ACE2 expression levels did not differ from controls at any timepoint, regardless of biologic or topical treatment. Conclusion: Significantly overexpressed levels of furin were observed in untreated patients, and, thus, these patients may be at risk for infection and a severe course of COVID-19. However, the data indicate that successful therapeutic intervention in psoriasis, by systemic biologic or topical treatment, can efficiently reduce furin levels in blood cells, possibly limiting the risk of psoriasis patients for a severe COVID-19 course. Clinical Trial Registration: ClinicalTrials.gov, identifier NCT02752672. Frontiers Media S.A. 2021-02-10 /pmc/articles/PMC7902756/ /pubmed/33644099 http://dx.doi.org/10.3389/fmed.2021.624462 Text en Copyright © 2021 Graier, Golob-Schwarzl, Weger, Benezeder, Painsi, Salmhofer and Wolf. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Graier, Thomas
Golob-Schwarzl, Nicole
Weger, Wolfgang
Benezeder, Theresa
Painsi, Clemens
Salmhofer, Wolfgang
Wolf, Peter
Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title_full Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title_fullStr Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title_full_unstemmed Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title_short Furin Expression in Patients With Psoriasis—A Patient Cohort Endangered to SARS-COV2?
title_sort furin expression in patients with psoriasis—a patient cohort endangered to sars-cov2?
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902756/
https://www.ncbi.nlm.nih.gov/pubmed/33644099
http://dx.doi.org/10.3389/fmed.2021.624462
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