Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Memórias do Instituto Oswaldo Cruz |
Texto Completo: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000900017 |
Resumo: | New Mycobacterium leprae protein antigens can contribute to improved serologic tests for leprosy diagnosis/classification and multidrug therapy (MDT) monitoring. This study describes seroreactivity to M. leprae proteins among participants from three highly endemic leprosy areas in Brazil: central-western Goiânia/Goiás (GO) (n = 225), Rondonópolis/Mato Grosso (MT) (n = 764) and northern Prata Village/Pará (PA) (n = 93). ELISA was performed to detect IgG to proteins (92f, 46f, leprosy IDRI diagnostic-1, ML0405, ML1213) and IgM to phenolic glycolipid-I (PGL-I). Multibacillary (MB) leprosy had positive rates for PGL-I that were similar to those for proteins; however, some anti-PGL-I-negative subjects were positive for proteins, suggesting that adding protein antigen to PGL-I can enhance the sensitivity of MB leprosy detection. In MT, different degrees of seroreactivity were observed and ranked for MB, former patients after MDT, paucibacillary (PB) leprosy, household contact (HHC) and endemic control (EC) groups. The seroreactivity of PB patients was low in GO and MT. HHCs from different endemic sites had similar IgG antibody responses to proteins. 46f and 92f were not recognised by most tuberculosis patients, ECs or HHCs within GO, an area with high BCG vaccination coverage. Low positivity in EC and HHC was observed in PA and MT. Our results provide evidence for the development of an improved serologic test that could be widely applicable for MB leprosy testing in Brazil. |
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Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in BrazilleprosydiagnosisserologyNew Mycobacterium leprae protein antigens can contribute to improved serologic tests for leprosy diagnosis/classification and multidrug therapy (MDT) monitoring. This study describes seroreactivity to M. leprae proteins among participants from three highly endemic leprosy areas in Brazil: central-western Goiânia/Goiás (GO) (n = 225), Rondonópolis/Mato Grosso (MT) (n = 764) and northern Prata Village/Pará (PA) (n = 93). ELISA was performed to detect IgG to proteins (92f, 46f, leprosy IDRI diagnostic-1, ML0405, ML1213) and IgM to phenolic glycolipid-I (PGL-I). Multibacillary (MB) leprosy had positive rates for PGL-I that were similar to those for proteins; however, some anti-PGL-I-negative subjects were positive for proteins, suggesting that adding protein antigen to PGL-I can enhance the sensitivity of MB leprosy detection. In MT, different degrees of seroreactivity were observed and ranked for MB, former patients after MDT, paucibacillary (PB) leprosy, household contact (HHC) and endemic control (EC) groups. The seroreactivity of PB patients was low in GO and MT. HHCs from different endemic sites had similar IgG antibody responses to proteins. 46f and 92f were not recognised by most tuberculosis patients, ECs or HHCs within GO, an area with high BCG vaccination coverage. Low positivity in EC and HHC was observed in PA and MT. Our results provide evidence for the development of an improved serologic test that could be widely applicable for MB leprosy testing in Brazil.Instituto Oswaldo Cruz, Ministério da Saúde2012-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000900017Memórias do Instituto Oswaldo Cruz v.107 suppl.1 2012reponame:Memórias do Instituto Oswaldo Cruzinstname:Fundação Oswaldo Cruzinstacron:FIOCRUZ10.1590/S0074-02762012000900017info:eu-repo/semantics/openAccessHungria,Emerith MayraOliveira,Regiane Morillas deSouza,Ana Lúcia Osório Maroclo deCosta,Maurício BarcelosSouza,Vânia Nieto Brito deSilva,Eliane AparecidaMoreno,Fátima Regina VilaniNogueira,Maria Esther SallesCosta,Maria Renata Sales NogueiraSilva,Sônia Maria Usó RuizBührer-Sékula,SamiraReed,Steven GDuthie,Malcolm SStefani,Mariane Martins de Araújoeng2020-04-25T17:51:21Zhttp://www.scielo.br/oai/scielo-oai.php0074-02761678-8060opendoar:null2020-04-26 02:18:44.376Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruztrue |
dc.title.none.fl_str_mv |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
title |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
spellingShingle |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil Hungria,Emerith Mayra leprosy diagnosis serology |
title_short |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
title_full |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
title_fullStr |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
title_full_unstemmed |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
title_sort |
Seroreactivity to new Mycobacterium leprae protein antigens in different leprosy-endemic regions in Brazil |
author |
Hungria,Emerith Mayra |
author_facet |
Hungria,Emerith Mayra Oliveira,Regiane Morillas de Souza,Ana Lúcia Osório Maroclo de Costa,Maurício Barcelos Souza,Vânia Nieto Brito de Silva,Eliane Aparecida Moreno,Fátima Regina Vilani Nogueira,Maria Esther Salles Costa,Maria Renata Sales Nogueira Silva,Sônia Maria Usó Ruiz Bührer-Sékula,Samira Reed,Steven G Duthie,Malcolm S Stefani,Mariane Martins de Araújo |
author_role |
author |
author2 |
Oliveira,Regiane Morillas de Souza,Ana Lúcia Osório Maroclo de Costa,Maurício Barcelos Souza,Vânia Nieto Brito de Silva,Eliane Aparecida Moreno,Fátima Regina Vilani Nogueira,Maria Esther Salles Costa,Maria Renata Sales Nogueira Silva,Sônia Maria Usó Ruiz Bührer-Sékula,Samira Reed,Steven G Duthie,Malcolm S Stefani,Mariane Martins de Araújo |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Hungria,Emerith Mayra Oliveira,Regiane Morillas de Souza,Ana Lúcia Osório Maroclo de Costa,Maurício Barcelos Souza,Vânia Nieto Brito de Silva,Eliane Aparecida Moreno,Fátima Regina Vilani Nogueira,Maria Esther Salles Costa,Maria Renata Sales Nogueira Silva,Sônia Maria Usó Ruiz Bührer-Sékula,Samira Reed,Steven G Duthie,Malcolm S Stefani,Mariane Martins de Araújo |
dc.subject.por.fl_str_mv |
leprosy diagnosis serology |
topic |
leprosy diagnosis serology |
dc.description.none.fl_txt_mv |
New Mycobacterium leprae protein antigens can contribute to improved serologic tests for leprosy diagnosis/classification and multidrug therapy (MDT) monitoring. This study describes seroreactivity to M. leprae proteins among participants from three highly endemic leprosy areas in Brazil: central-western Goiânia/Goiás (GO) (n = 225), Rondonópolis/Mato Grosso (MT) (n = 764) and northern Prata Village/Pará (PA) (n = 93). ELISA was performed to detect IgG to proteins (92f, 46f, leprosy IDRI diagnostic-1, ML0405, ML1213) and IgM to phenolic glycolipid-I (PGL-I). Multibacillary (MB) leprosy had positive rates for PGL-I that were similar to those for proteins; however, some anti-PGL-I-negative subjects were positive for proteins, suggesting that adding protein antigen to PGL-I can enhance the sensitivity of MB leprosy detection. In MT, different degrees of seroreactivity were observed and ranked for MB, former patients after MDT, paucibacillary (PB) leprosy, household contact (HHC) and endemic control (EC) groups. The seroreactivity of PB patients was low in GO and MT. HHCs from different endemic sites had similar IgG antibody responses to proteins. 46f and 92f were not recognised by most tuberculosis patients, ECs or HHCs within GO, an area with high BCG vaccination coverage. Low positivity in EC and HHC was observed in PA and MT. Our results provide evidence for the development of an improved serologic test that could be widely applicable for MB leprosy testing in Brazil. |
description |
New Mycobacterium leprae protein antigens can contribute to improved serologic tests for leprosy diagnosis/classification and multidrug therapy (MDT) monitoring. This study describes seroreactivity to M. leprae proteins among participants from three highly endemic leprosy areas in Brazil: central-western Goiânia/Goiás (GO) (n = 225), Rondonópolis/Mato Grosso (MT) (n = 764) and northern Prata Village/Pará (PA) (n = 93). ELISA was performed to detect IgG to proteins (92f, 46f, leprosy IDRI diagnostic-1, ML0405, ML1213) and IgM to phenolic glycolipid-I (PGL-I). Multibacillary (MB) leprosy had positive rates for PGL-I that were similar to those for proteins; however, some anti-PGL-I-negative subjects were positive for proteins, suggesting that adding protein antigen to PGL-I can enhance the sensitivity of MB leprosy detection. In MT, different degrees of seroreactivity were observed and ranked for MB, former patients after MDT, paucibacillary (PB) leprosy, household contact (HHC) and endemic control (EC) groups. The seroreactivity of PB patients was low in GO and MT. HHCs from different endemic sites had similar IgG antibody responses to proteins. 46f and 92f were not recognised by most tuberculosis patients, ECs or HHCs within GO, an area with high BCG vaccination coverage. Low positivity in EC and HHC was observed in PA and MT. Our results provide evidence for the development of an improved serologic test that could be widely applicable for MB leprosy testing in Brazil. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000900017 |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762012000900017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0074-02762012000900017 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
dc.source.none.fl_str_mv |
Memórias do Instituto Oswaldo Cruz v.107 suppl.1 2012 reponame:Memórias do Instituto Oswaldo Cruz instname:Fundação Oswaldo Cruz instacron:FIOCRUZ |
reponame_str |
Memórias do Instituto Oswaldo Cruz |
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Memórias do Instituto Oswaldo Cruz |
instname_str |
Fundação Oswaldo Cruz |
instacron_str |
FIOCRUZ |
institution |
FIOCRUZ |
repository.name.fl_str_mv |
Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruz |
repository.mail.fl_str_mv |
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1669937713015422976 |