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Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases
After sustained exposure to Mycobacterium leprae, only a subset of exposed individuals develops clinical leprosy. Moreover, leprosy patients show a wide spectrum of clinical manifestations that extend from the paucibacillary (PB) to the multibacillary (MB) form of the disease. This “polarization” of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878860/ https://www.ncbi.nlm.nih.gov/pubmed/27219008 http://dx.doi.org/10.1371/journal.pntd.0004345 |
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author | Gaschignard, Jean Grant, Audrey Virginia Thuc, Nguyen Van Orlova, Marianna Cobat, Aurélie Huong, Nguyen Thu Ba, Nguyen Ngoc Thai, Vu Hong Abel, Laurent Schurr, Erwin Alcaïs, Alexandre |
author_facet | Gaschignard, Jean Grant, Audrey Virginia Thuc, Nguyen Van Orlova, Marianna Cobat, Aurélie Huong, Nguyen Thu Ba, Nguyen Ngoc Thai, Vu Hong Abel, Laurent Schurr, Erwin Alcaïs, Alexandre |
author_sort | Gaschignard, Jean |
collection | PubMed |
description | After sustained exposure to Mycobacterium leprae, only a subset of exposed individuals develops clinical leprosy. Moreover, leprosy patients show a wide spectrum of clinical manifestations that extend from the paucibacillary (PB) to the multibacillary (MB) form of the disease. This “polarization” of leprosy has long been a major focus of investigation for immunologists because of the different immune response in these two forms. But while leprosy per se has been shown to be under tight human genetic control, few epidemiological or genetic studies have focused on leprosy subtypes. Using PubMed, we collected available data in English on the epidemiology of leprosy polarization and the possible role of human genetics in its pathophysiology until September 2015. At the genetic level, we assembled a list of 28 genes from the literature that are associated with leprosy subtypes or implicated in the polarization process. Our bibliographical search revealed that improved study designs are needed to identify genes associated with leprosy polarization. Future investigations should not be restricted to a subanalysis of leprosy per se studies but should instead contrast MB to PB individuals. We show the latter approach to be the most powerful design for the identification of genetic polarization determinants. Finally, we bring to light the important resource represented by the nine-banded armadillo model, a unique animal model for leprosy. |
format | Online Article Text |
id | pubmed-4878860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48788602016-06-09 Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases Gaschignard, Jean Grant, Audrey Virginia Thuc, Nguyen Van Orlova, Marianna Cobat, Aurélie Huong, Nguyen Thu Ba, Nguyen Ngoc Thai, Vu Hong Abel, Laurent Schurr, Erwin Alcaïs, Alexandre PLoS Negl Trop Dis Review After sustained exposure to Mycobacterium leprae, only a subset of exposed individuals develops clinical leprosy. Moreover, leprosy patients show a wide spectrum of clinical manifestations that extend from the paucibacillary (PB) to the multibacillary (MB) form of the disease. This “polarization” of leprosy has long been a major focus of investigation for immunologists because of the different immune response in these two forms. But while leprosy per se has been shown to be under tight human genetic control, few epidemiological or genetic studies have focused on leprosy subtypes. Using PubMed, we collected available data in English on the epidemiology of leprosy polarization and the possible role of human genetics in its pathophysiology until September 2015. At the genetic level, we assembled a list of 28 genes from the literature that are associated with leprosy subtypes or implicated in the polarization process. Our bibliographical search revealed that improved study designs are needed to identify genes associated with leprosy polarization. Future investigations should not be restricted to a subanalysis of leprosy per se studies but should instead contrast MB to PB individuals. We show the latter approach to be the most powerful design for the identification of genetic polarization determinants. Finally, we bring to light the important resource represented by the nine-banded armadillo model, a unique animal model for leprosy. Public Library of Science 2016-05-24 /pmc/articles/PMC4878860/ /pubmed/27219008 http://dx.doi.org/10.1371/journal.pntd.0004345 Text en © 2016 Gaschignard et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Gaschignard, Jean Grant, Audrey Virginia Thuc, Nguyen Van Orlova, Marianna Cobat, Aurélie Huong, Nguyen Thu Ba, Nguyen Ngoc Thai, Vu Hong Abel, Laurent Schurr, Erwin Alcaïs, Alexandre Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title | Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title_full | Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title_fullStr | Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title_full_unstemmed | Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title_short | Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases |
title_sort | pauci- and multibacillary leprosy: two distinct, genetically neglected diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878860/ https://www.ncbi.nlm.nih.gov/pubmed/27219008 http://dx.doi.org/10.1371/journal.pntd.0004345 |
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