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Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)

Segmental vitiligo (SV) is a unilateral subtype of vitiligo which is clinically characterized by a cutaneous depigmentation and histologically by a melanocyte loss from the epidermis and hair follicle reservoirs. To date, its pathogenesis remains a mystery. In many cases, this skin depigmentation sh...

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Autores principales: Gauthier, Yvon, Lepreux, Sebastien, Cario‐Andre, Muriel, Rambert, Jérome, Dakdaki, Adrien, Lafon, Marie‐Edith, Abouqal, Redouane, Benzekri, Laila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092484/
https://www.ncbi.nlm.nih.gov/pubmed/36112095
http://dx.doi.org/10.1111/pcmr.13064
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author Gauthier, Yvon
Lepreux, Sebastien
Cario‐Andre, Muriel
Rambert, Jérome
Dakdaki, Adrien
Lafon, Marie‐Edith
Abouqal, Redouane
Benzekri, Laila
author_facet Gauthier, Yvon
Lepreux, Sebastien
Cario‐Andre, Muriel
Rambert, Jérome
Dakdaki, Adrien
Lafon, Marie‐Edith
Abouqal, Redouane
Benzekri, Laila
author_sort Gauthier, Yvon
collection PubMed
description Segmental vitiligo (SV) is a unilateral subtype of vitiligo which is clinically characterized by a cutaneous depigmentation and histologically by a melanocyte loss from the epidermis and hair follicle reservoirs. To date, its pathogenesis remains a mystery. In many cases, this skin depigmentation shares several clinical features and dysfunctions with herpes zoster (HZ). So, for the first time, we examined whether any nucleus and cell fusion associated with a positive immunolabelling of varicella‐zoster virus (VZV) and VZV mature virions could be found in SV skin samples as in herpes zoster (HZ). A total of 40 SV samples were used for histological and immunochemical studies. Control samples were obtained from three HZ, and 10 generalized vitiligo lesions. For ultrastructural study, three recent SV and one HZ as controls were recruited. Here, we report that nuclear fusion in epidermal cells were statistically associated with recent SV (p < .001), whereas syncytia formation was associated with long‐lasting SV (p = .001). A positive detection of VZV antigen was statistically associated in the epidermis with recent SV and in the dermis with long‐lasting SV (p = .001). Finally, the discovery of mature virions in 3/3 recent SV samples provides additional arguments for our viral hypothesis.
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spelling pubmed-100924842023-04-13 Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study) Gauthier, Yvon Lepreux, Sebastien Cario‐Andre, Muriel Rambert, Jérome Dakdaki, Adrien Lafon, Marie‐Edith Abouqal, Redouane Benzekri, Laila Pigment Cell Melanoma Res Short Communications Segmental vitiligo (SV) is a unilateral subtype of vitiligo which is clinically characterized by a cutaneous depigmentation and histologically by a melanocyte loss from the epidermis and hair follicle reservoirs. To date, its pathogenesis remains a mystery. In many cases, this skin depigmentation shares several clinical features and dysfunctions with herpes zoster (HZ). So, for the first time, we examined whether any nucleus and cell fusion associated with a positive immunolabelling of varicella‐zoster virus (VZV) and VZV mature virions could be found in SV skin samples as in herpes zoster (HZ). A total of 40 SV samples were used for histological and immunochemical studies. Control samples were obtained from three HZ, and 10 generalized vitiligo lesions. For ultrastructural study, three recent SV and one HZ as controls were recruited. Here, we report that nuclear fusion in epidermal cells were statistically associated with recent SV (p < .001), whereas syncytia formation was associated with long‐lasting SV (p = .001). A positive detection of VZV antigen was statistically associated in the epidermis with recent SV and in the dermis with long‐lasting SV (p = .001). Finally, the discovery of mature virions in 3/3 recent SV samples provides additional arguments for our viral hypothesis. John Wiley and Sons Inc. 2022-10-09 2023-01 /pmc/articles/PMC10092484/ /pubmed/36112095 http://dx.doi.org/10.1111/pcmr.13064 Text en © 2022 The Authors. Pigment Cell & Melanoma Research published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Gauthier, Yvon
Lepreux, Sebastien
Cario‐Andre, Muriel
Rambert, Jérome
Dakdaki, Adrien
Lafon, Marie‐Edith
Abouqal, Redouane
Benzekri, Laila
Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title_full Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title_fullStr Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title_full_unstemmed Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title_short Varicella‐zoster virus in actively spreading segmental vitiligo skin: Pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
title_sort varicella‐zoster virus in actively spreading segmental vitiligo skin: pathological, immunochemical, and ultrastructural findings (a first and preliminary study)
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092484/
https://www.ncbi.nlm.nih.gov/pubmed/36112095
http://dx.doi.org/10.1111/pcmr.13064
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