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Endemic pemphigus over a century: Part II

BACKGROUND: Endemic pemphigus foliaceus (EPF) is an autoimmune disease, classically occurring in a restricted geographic area. Foci of EPF have been described in several Central and South American countries, often affecting young people and Amerindians, with some female predilection. Although most A...

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Autores principales: Abréu-Vélez, Ana María, Roselino, Ana Maria, Howard, Michael S., Reason, Iara J. de Messias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354423/
https://www.ncbi.nlm.nih.gov/pubmed/22624125
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author Abréu-Vélez, Ana María
Roselino, Ana Maria
Howard, Michael S.
Reason, Iara J. de Messias
author_facet Abréu-Vélez, Ana María
Roselino, Ana Maria
Howard, Michael S.
Reason, Iara J. de Messias
author_sort Abréu-Vélez, Ana María
collection PubMed
description BACKGROUND: Endemic pemphigus foliaceus (EPF) is an autoimmune disease, classically occurring in a restricted geographic area. Foci of EPF have been described in several Central and South American countries, often affecting young people and Amerindians, with some female predilection. Although most American EPF cases have been documented in Brazil, cases have been reported in Peru, Paraguay, El Salvador and Venezuela. An additional variant of EPF has been described in El Bagre, Colombia, (El Bagre-EPF) affecting older men and a few post-menopausal females. Finally, one additional type of EPF has been described in nomadic tribes affecting females of child bearing age in Tunisia, Africa. AIMS: The main aim of this review is to summarize current knowledge about autoantigens, and immunologic and genetic studies in EPF. MATERIAL AND METHODS: We utilized a retrospective review of the literature, aiming to compile and compare the multiple geographic foci of EPF. RESULTS: The primary autoantigens in EPF are still considered to be desmogleins in the case of the Tunisian and all American cases, in contradistinction to plakins and desmogleins in El Bagre-EPF. Although several autoantigens are been suggested, their biochemical nature needs further elucidation. Current knowledge still supports the concept that an antibody mediated immune response represents the principal pathophysiology in all variants of EPF. CONCLUSION: A strong genetic susceptibility appears to contribute to disease development in several people affected by these diseases; however, no specific genes have been confirmed at present. We conclude that further investigation is necessary to define these disorders immunologically and genetically.
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spelling pubmed-33544232012-05-23 Endemic pemphigus over a century: Part II Abréu-Vélez, Ana María Roselino, Ana Maria Howard, Michael S. Reason, Iara J. de Messias N Am J Med Sci Review Article BACKGROUND: Endemic pemphigus foliaceus (EPF) is an autoimmune disease, classically occurring in a restricted geographic area. Foci of EPF have been described in several Central and South American countries, often affecting young people and Amerindians, with some female predilection. Although most American EPF cases have been documented in Brazil, cases have been reported in Peru, Paraguay, El Salvador and Venezuela. An additional variant of EPF has been described in El Bagre, Colombia, (El Bagre-EPF) affecting older men and a few post-menopausal females. Finally, one additional type of EPF has been described in nomadic tribes affecting females of child bearing age in Tunisia, Africa. AIMS: The main aim of this review is to summarize current knowledge about autoantigens, and immunologic and genetic studies in EPF. MATERIAL AND METHODS: We utilized a retrospective review of the literature, aiming to compile and compare the multiple geographic foci of EPF. RESULTS: The primary autoantigens in EPF are still considered to be desmogleins in the case of the Tunisian and all American cases, in contradistinction to plakins and desmogleins in El Bagre-EPF. Although several autoantigens are been suggested, their biochemical nature needs further elucidation. Current knowledge still supports the concept that an antibody mediated immune response represents the principal pathophysiology in all variants of EPF. CONCLUSION: A strong genetic susceptibility appears to contribute to disease development in several people affected by these diseases; however, no specific genes have been confirmed at present. We conclude that further investigation is necessary to define these disorders immunologically and genetically. Medknow Publications & Media Pvt Ltd 2010-03 /pmc/articles/PMC3354423/ /pubmed/22624125 Text en Copyright: © North American Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Abréu-Vélez, Ana María
Roselino, Ana Maria
Howard, Michael S.
Reason, Iara J. de Messias
Endemic pemphigus over a century: Part II
title Endemic pemphigus over a century: Part II
title_full Endemic pemphigus over a century: Part II
title_fullStr Endemic pemphigus over a century: Part II
title_full_unstemmed Endemic pemphigus over a century: Part II
title_short Endemic pemphigus over a century: Part II
title_sort endemic pemphigus over a century: part ii
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354423/
https://www.ncbi.nlm.nih.gov/pubmed/22624125
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