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Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris

BACKGROUND: Common warts are caused by human papillomaviruses (HPVs), they are among the most common cutaneous viral infections. Macrophage migration inhibitory factor (MIF) is an essential contributor in many inflammatory and immune skin diseases. Yet, its role in the pathology of common warts is u...

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Autores principales: Sorour, Neveen Emad, Hamed, Ahmed Mohamed, Tabl, Hala Abd-El Mageed, Ahmed, Amira Abd-El Aziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709820/
https://www.ncbi.nlm.nih.gov/pubmed/31686887
http://dx.doi.org/10.2147/CCID.S209269
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author Sorour, Neveen Emad
Hamed, Ahmed Mohamed
Tabl, Hala Abd-El Mageed
Ahmed, Amira Abd-El Aziz
author_facet Sorour, Neveen Emad
Hamed, Ahmed Mohamed
Tabl, Hala Abd-El Mageed
Ahmed, Amira Abd-El Aziz
author_sort Sorour, Neveen Emad
collection PubMed
description BACKGROUND: Common warts are caused by human papillomaviruses (HPVs), they are among the most common cutaneous viral infections. Macrophage migration inhibitory factor (MIF) is an essential contributor in many inflammatory and immune skin diseases. Yet, its role in the pathology of common warts is unclear. OBJECTIVE: To assess MIF levels in lesional and perilesional skin in patients with common warts in comparison to apparently healthy control group with matching age and sex. SUBJECTS AND METHODS: A case-control study performed on 60 patients with common warts (group A) and 30 age and sex matching healthy controls (group B). Two biopsies were taken from each patient in group A; one from the lesion (lesional) and the other one from the skin around the wart (perilesional), while biopsies of controls were taken from matched sites to patients. Measurement of MIF in all groups was done by quantitative ELISA kits. RESULTS: Significant high MIF levels were detected in lesional and perilesional skin biopsies compared to controls (P<0.001). Yet, the difference in MIF levels between lesional and perilesional skin biopsy was non-significant. No significant relations were found between lesional and perilesional MIF levels and clinical characteristics of the studied patients while both lesional and perilesional MIF levels were significantly correlated (rh=0.269, P=0.021). CONCLUSION: The significantly elevated MIF levels in lesional and perilesional skin biopsies compared to controls point to its role in wart progression from HPV infected cells.
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spelling pubmed-67098202019-11-04 Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris Sorour, Neveen Emad Hamed, Ahmed Mohamed Tabl, Hala Abd-El Mageed Ahmed, Amira Abd-El Aziz Clin Cosmet Investig Dermatol Original Research BACKGROUND: Common warts are caused by human papillomaviruses (HPVs), they are among the most common cutaneous viral infections. Macrophage migration inhibitory factor (MIF) is an essential contributor in many inflammatory and immune skin diseases. Yet, its role in the pathology of common warts is unclear. OBJECTIVE: To assess MIF levels in lesional and perilesional skin in patients with common warts in comparison to apparently healthy control group with matching age and sex. SUBJECTS AND METHODS: A case-control study performed on 60 patients with common warts (group A) and 30 age and sex matching healthy controls (group B). Two biopsies were taken from each patient in group A; one from the lesion (lesional) and the other one from the skin around the wart (perilesional), while biopsies of controls were taken from matched sites to patients. Measurement of MIF in all groups was done by quantitative ELISA kits. RESULTS: Significant high MIF levels were detected in lesional and perilesional skin biopsies compared to controls (P<0.001). Yet, the difference in MIF levels between lesional and perilesional skin biopsy was non-significant. No significant relations were found between lesional and perilesional MIF levels and clinical characteristics of the studied patients while both lesional and perilesional MIF levels were significantly correlated (rh=0.269, P=0.021). CONCLUSION: The significantly elevated MIF levels in lesional and perilesional skin biopsies compared to controls point to its role in wart progression from HPV infected cells. Dove 2019-08-22 /pmc/articles/PMC6709820/ /pubmed/31686887 http://dx.doi.org/10.2147/CCID.S209269 Text en © 2019 Sorour et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Sorour, Neveen Emad
Hamed, Ahmed Mohamed
Tabl, Hala Abd-El Mageed
Ahmed, Amira Abd-El Aziz
Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title_full Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title_fullStr Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title_full_unstemmed Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title_short Assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
title_sort assessment of macrophage migration inhibitory factor in patients with verruca vulgaris
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709820/
https://www.ncbi.nlm.nih.gov/pubmed/31686887
http://dx.doi.org/10.2147/CCID.S209269
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