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Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved

Current treatment of vitiligo is still a great challenge, since most cases of vitiligo have variable re-pigmentation outcomes due to their unpredictable responses to existing therapeutic regimens. There is an urgent need to identify this re-pigmentation process and to develop novel therapies. This r...

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Autores principales: Lei, Tie-Chi, Hearing, Vincent J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249724/
https://www.ncbi.nlm.nih.gov/pubmed/32433056
http://dx.doi.org/10.1097/CM9.0000000000000794
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author Lei, Tie-Chi
Hearing, Vincent J.
author_facet Lei, Tie-Chi
Hearing, Vincent J.
author_sort Lei, Tie-Chi
collection PubMed
description Current treatment of vitiligo is still a great challenge, since most cases of vitiligo have variable re-pigmentation outcomes due to their unpredictable responses to existing therapeutic regimens. There is an urgent need to identify this re-pigmentation process and to develop novel therapies. This review illustrates the most current research and latest understanding of vitiligo skin re-pigmentation and related regulatory mechanisms. Literature was collected from PubMed until January 2020, using the search terms including “vitiligo,” “re-pigmentation,” “phototherapy,” “narrow-band ultraviolet B, ” “excimer,” “fractional carbon dioxide laser,” and “melanocyte stem cells.” Literature was mainly derived from English articles. Article type was not limited. Emerging evidence suggests that patients with vitiligo present various re-pigmentation patterns following ultraviolet B phototherapy, which relies on different cell reservoirs from the perilesional margins and/or from uninvolved hair follicles to replenish functional melanocytes that are lost in vitiliginous skin. The following events are likely to be involved in this re-pigmentation process, including: 1) changes in the paracrine secretion and distribution of transforming growth factor-β1 in the bulge area and in the epidermis; 2) the enhanced transfer of dermal pro-melanogenic growth factors to the epidermis; and 3) the induction of a C-X-C motif chemokine ligand (CXCL) 12-enriched micro-environment that efficiently recruits CXCR4- or CXCR7-positive melanocytes. Ongoing studies on the cellular and molecular events underlying vitiligo re-pigmentation will help design new therapeutic strategies to improve treatment outcomes.
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spelling pubmed-72497242020-06-15 Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved Lei, Tie-Chi Hearing, Vincent J. Chin Med J (Engl) Review Articles Current treatment of vitiligo is still a great challenge, since most cases of vitiligo have variable re-pigmentation outcomes due to their unpredictable responses to existing therapeutic regimens. There is an urgent need to identify this re-pigmentation process and to develop novel therapies. This review illustrates the most current research and latest understanding of vitiligo skin re-pigmentation and related regulatory mechanisms. Literature was collected from PubMed until January 2020, using the search terms including “vitiligo,” “re-pigmentation,” “phototherapy,” “narrow-band ultraviolet B, ” “excimer,” “fractional carbon dioxide laser,” and “melanocyte stem cells.” Literature was mainly derived from English articles. Article type was not limited. Emerging evidence suggests that patients with vitiligo present various re-pigmentation patterns following ultraviolet B phototherapy, which relies on different cell reservoirs from the perilesional margins and/or from uninvolved hair follicles to replenish functional melanocytes that are lost in vitiliginous skin. The following events are likely to be involved in this re-pigmentation process, including: 1) changes in the paracrine secretion and distribution of transforming growth factor-β1 in the bulge area and in the epidermis; 2) the enhanced transfer of dermal pro-melanogenic growth factors to the epidermis; and 3) the induction of a C-X-C motif chemokine ligand (CXCL) 12-enriched micro-environment that efficiently recruits CXCR4- or CXCR7-positive melanocytes. Ongoing studies on the cellular and molecular events underlying vitiligo re-pigmentation will help design new therapeutic strategies to improve treatment outcomes. Wolters Kluwer Health 2020-05-20 2020-04-21 /pmc/articles/PMC7249724/ /pubmed/32433056 http://dx.doi.org/10.1097/CM9.0000000000000794 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Review Articles
Lei, Tie-Chi
Hearing, Vincent J.
Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title_full Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title_fullStr Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title_full_unstemmed Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title_short Deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
title_sort deciphering skin re-pigmentation patterns in vitiligo: an update on the cellular and molecular events involved
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249724/
https://www.ncbi.nlm.nih.gov/pubmed/32433056
http://dx.doi.org/10.1097/CM9.0000000000000794
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