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Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies

The number of new cases of leprosy reported worldwide has remained essentially unchanged for the last decade despite continued global use of free multidrug therapy (MDT) provided to any diagnosed leprosy patient. In order to more effectively interrupt the chain of transmission, new strategies will b...

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Autores principales: da Silva, Moises Batista, Li, Wei, Bouth, Raquel Carvalho, Gobbo, Angélica Rita, Messias, Ana Caroline Cunha, Moraes, Tania Mara Pires, Jorge, Erika Vanessa Oliveira, Barreto, Josafá Gonçalves, Filho, Fred Bernardes, Conde, Guilherme Augusto Barros, Frade, Marco Andrey Cipriani, Salgado, Claudio Guedes, Spencer, John Stewart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118453/
https://www.ncbi.nlm.nih.gov/pubmed/33984058
http://dx.doi.org/10.1371/journal.pone.0251631
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author da Silva, Moises Batista
Li, Wei
Bouth, Raquel Carvalho
Gobbo, Angélica Rita
Messias, Ana Caroline Cunha
Moraes, Tania Mara Pires
Jorge, Erika Vanessa Oliveira
Barreto, Josafá Gonçalves
Filho, Fred Bernardes
Conde, Guilherme Augusto Barros
Frade, Marco Andrey Cipriani
Salgado, Claudio Guedes
Spencer, John Stewart
author_facet da Silva, Moises Batista
Li, Wei
Bouth, Raquel Carvalho
Gobbo, Angélica Rita
Messias, Ana Caroline Cunha
Moraes, Tania Mara Pires
Jorge, Erika Vanessa Oliveira
Barreto, Josafá Gonçalves
Filho, Fred Bernardes
Conde, Guilherme Augusto Barros
Frade, Marco Andrey Cipriani
Salgado, Claudio Guedes
Spencer, John Stewart
author_sort da Silva, Moises Batista
collection PubMed
description The number of new cases of leprosy reported worldwide has remained essentially unchanged for the last decade despite continued global use of free multidrug therapy (MDT) provided to any diagnosed leprosy patient. In order to more effectively interrupt the chain of transmission, new strategies will be required to detect those with latent disease who contribute to furthering transmission. To improve the ability to diagnose leprosy earlier in asymptomatic infected individuals, we examined the combined use of two well-known biomarkers of M. leprae infection, namely the presence of M. leprae DNA by PCR from earlobe slit skin smears (SSS) and positive antibody titers to the M. leprae-specific antigen, Phenolic Glycolipid I (anti-PGL-I) from leprosy patients and household contacts living in seven hyperendemic cities in the northern state of Pará, Brazilian Amazon. Combining both tests increased sensitivity, specificity and accuracy over either test alone. A total of 466 individuals were evaluated, including 87 newly diagnosed leprosy patients, 52 post-treated patients, 296 household contacts and 31 healthy endemic controls. The highest frequency of double positives (PGL-I+/RLEP+) were detected in the new case group (40/87, 46%) with lower numbers for treated (12/52, 23.1%), household contacts (46/296, 15.5%) and healthy endemic controls (0/31, 0%). The frequencies in these groups were reversed for double negatives (PGL-I-/RLEP-) for new cases (6/87, 6.9%), treated leprosy cases (15/52, 28.8%) and the highest in household contacts (108/296, 36.5%) and healthy endemic controls (24/31, 77.4%). The data strongly suggest that household contacts that are double positive have latent disease, are likely contributing to shedding and transmission of disease to their close contacts and are at the highest risk of progressing to clinical disease. Proposed strategies to reduce leprosy transmission in highly endemic areas may include chemoprophylactic treatment of this group of individuals to stop the spread of bacilli to eventually lower new case detection rates in these areas.
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spelling pubmed-81184532021-05-24 Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies da Silva, Moises Batista Li, Wei Bouth, Raquel Carvalho Gobbo, Angélica Rita Messias, Ana Caroline Cunha Moraes, Tania Mara Pires Jorge, Erika Vanessa Oliveira Barreto, Josafá Gonçalves Filho, Fred Bernardes Conde, Guilherme Augusto Barros Frade, Marco Andrey Cipriani Salgado, Claudio Guedes Spencer, John Stewart PLoS One Research Article The number of new cases of leprosy reported worldwide has remained essentially unchanged for the last decade despite continued global use of free multidrug therapy (MDT) provided to any diagnosed leprosy patient. In order to more effectively interrupt the chain of transmission, new strategies will be required to detect those with latent disease who contribute to furthering transmission. To improve the ability to diagnose leprosy earlier in asymptomatic infected individuals, we examined the combined use of two well-known biomarkers of M. leprae infection, namely the presence of M. leprae DNA by PCR from earlobe slit skin smears (SSS) and positive antibody titers to the M. leprae-specific antigen, Phenolic Glycolipid I (anti-PGL-I) from leprosy patients and household contacts living in seven hyperendemic cities in the northern state of Pará, Brazilian Amazon. Combining both tests increased sensitivity, specificity and accuracy over either test alone. A total of 466 individuals were evaluated, including 87 newly diagnosed leprosy patients, 52 post-treated patients, 296 household contacts and 31 healthy endemic controls. The highest frequency of double positives (PGL-I+/RLEP+) were detected in the new case group (40/87, 46%) with lower numbers for treated (12/52, 23.1%), household contacts (46/296, 15.5%) and healthy endemic controls (0/31, 0%). The frequencies in these groups were reversed for double negatives (PGL-I-/RLEP-) for new cases (6/87, 6.9%), treated leprosy cases (15/52, 28.8%) and the highest in household contacts (108/296, 36.5%) and healthy endemic controls (24/31, 77.4%). The data strongly suggest that household contacts that are double positive have latent disease, are likely contributing to shedding and transmission of disease to their close contacts and are at the highest risk of progressing to clinical disease. Proposed strategies to reduce leprosy transmission in highly endemic areas may include chemoprophylactic treatment of this group of individuals to stop the spread of bacilli to eventually lower new case detection rates in these areas. Public Library of Science 2021-05-13 /pmc/articles/PMC8118453/ /pubmed/33984058 http://dx.doi.org/10.1371/journal.pone.0251631 Text en © 2021 da Silva et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Research Article
da Silva, Moises Batista
Li, Wei
Bouth, Raquel Carvalho
Gobbo, Angélica Rita
Messias, Ana Caroline Cunha
Moraes, Tania Mara Pires
Jorge, Erika Vanessa Oliveira
Barreto, Josafá Gonçalves
Filho, Fred Bernardes
Conde, Guilherme Augusto Barros
Frade, Marco Andrey Cipriani
Salgado, Claudio Guedes
Spencer, John Stewart
Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title_full Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title_fullStr Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title_full_unstemmed Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title_short Latent leprosy infection identified by dual RLEP and anti-PGL-I positivity: Implications for new control strategies
title_sort latent leprosy infection identified by dual rlep and anti-pgl-i positivity: implications for new control strategies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118453/
https://www.ncbi.nlm.nih.gov/pubmed/33984058
http://dx.doi.org/10.1371/journal.pone.0251631
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