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Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne

Adult female acne is a chronic inflammatory, immune-mediated disease that affects the pilosebaceous unit in women in their 20s to 40s, and is considered different from acne vulgaris. Propionibacterium acnes is recognized by TLR-2, resulting in activation of this receptor and an inflammatory response...

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Autores principales: Rocha, Marco A. D., Guadanhim, Lilia R. S., Sanudo, Adriana, Bagatin, Edileia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821154/
https://www.ncbi.nlm.nih.gov/pubmed/29484093
http://dx.doi.org/10.1080/19381980.2017.1361570
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author Rocha, Marco A. D.
Guadanhim, Lilia R. S.
Sanudo, Adriana
Bagatin, Edileia
author_facet Rocha, Marco A. D.
Guadanhim, Lilia R. S.
Sanudo, Adriana
Bagatin, Edileia
author_sort Rocha, Marco A. D.
collection PubMed
description Adult female acne is a chronic inflammatory, immune-mediated disease that affects the pilosebaceous unit in women in their 20s to 40s, and is considered different from acne vulgaris. Propionibacterium acnes is recognized by TLR-2, resulting in activation of this receptor and an inflammatory response through the NFκ B pathway. This therapeutic, interventional, open, randomized, evaluator-blinded and comparative trial included 38 adult women with moderate facial acne and 10 age-matched controls, all aged between 26 and 44 years. Two treatments were performed over six months: 15% azelaic acid gel (AA) bid (n = 18) and oral contraceptive (COC) drospirenone 3 mg/ethinylestradiol .02 mg (n = 20). Biopsies were taken at baseline (control, lesion, perilesional) and at the conclusion (lesion and perilesional) of the study to evaluate TLR-2 expression by immunohistochemistry. Lesion count and blind photographic evaluation were used for efficacy. The groups were homogeneous: 70% of lesions were located in the submandibular area, 95% of participants had inflammatory lesions; of these, 50% had persistent and 50% had late-onset acne. The mean ages were 33.7 ± 5.5 and 33.1 ± 5.3 years (COC and AA group, respectively). A moderate clinical improvement was observed in both groups. No difference in TLR-2 expression in the lesion or perilesional areas was observed; however, reduced TLR-2 expression was seen in the control group. A significant reduction in expression was observed after both treatments, with no difference between the groups. This finding suggests an anti-inflammatory effect of COCs and AA in adult female acne, via modulation of the TLR-2 receptor.
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spelling pubmed-58211542018-02-26 Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne Rocha, Marco A. D. Guadanhim, Lilia R. S. Sanudo, Adriana Bagatin, Edileia Dermatoendocrinol Research Paper Adult female acne is a chronic inflammatory, immune-mediated disease that affects the pilosebaceous unit in women in their 20s to 40s, and is considered different from acne vulgaris. Propionibacterium acnes is recognized by TLR-2, resulting in activation of this receptor and an inflammatory response through the NFκ B pathway. This therapeutic, interventional, open, randomized, evaluator-blinded and comparative trial included 38 adult women with moderate facial acne and 10 age-matched controls, all aged between 26 and 44 years. Two treatments were performed over six months: 15% azelaic acid gel (AA) bid (n = 18) and oral contraceptive (COC) drospirenone 3 mg/ethinylestradiol .02 mg (n = 20). Biopsies were taken at baseline (control, lesion, perilesional) and at the conclusion (lesion and perilesional) of the study to evaluate TLR-2 expression by immunohistochemistry. Lesion count and blind photographic evaluation were used for efficacy. The groups were homogeneous: 70% of lesions were located in the submandibular area, 95% of participants had inflammatory lesions; of these, 50% had persistent and 50% had late-onset acne. The mean ages were 33.7 ± 5.5 and 33.1 ± 5.3 years (COC and AA group, respectively). A moderate clinical improvement was observed in both groups. No difference in TLR-2 expression in the lesion or perilesional areas was observed; however, reduced TLR-2 expression was seen in the control group. A significant reduction in expression was observed after both treatments, with no difference between the groups. This finding suggests an anti-inflammatory effect of COCs and AA in adult female acne, via modulation of the TLR-2 receptor. Taylor & Francis 2017-10-04 /pmc/articles/PMC5821154/ /pubmed/29484093 http://dx.doi.org/10.1080/19381980.2017.1361570 Text en © 2018 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Rocha, Marco A. D.
Guadanhim, Lilia R. S.
Sanudo, Adriana
Bagatin, Edileia
Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title_full Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title_fullStr Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title_full_unstemmed Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title_short Modulation of Toll Like Receptor-2 on sebaceous gland by the treatment of adult female acne
title_sort modulation of toll like receptor-2 on sebaceous gland by the treatment of adult female acne
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821154/
https://www.ncbi.nlm.nih.gov/pubmed/29484093
http://dx.doi.org/10.1080/19381980.2017.1361570
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