Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Sandra Lucia Euzebio [UNIFESP]
Data de Publicação: 2011
Outros Autores: Pereira, Helena Lúcia Alves [UNIFESP], Silva, Neusa Pereira da [UNIFESP], Souza, Alexandre Wagner Silva de [UNIFESP], Sato, Emilia Inoue [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://www.actareumatologica.pt/article_download.php?id=648
https://repositorio.unifesp.br/handle/11600/42090
Resumo: Objectives: To determine the prevalence of anticardiolipin (aCL) and anti-beta(2)-glycoprotein I (anti-beta(2)GPI) antibodies in leprosy patients, during and after specific multidrug therapy (MDT), and to evaluate a possible association between these antibodies and some clinical characteristics of leprosy, including clinical forms, reactional episodes and treatment.Methods: The study included 158 leprosy patients, 129 gender-and-age matched healthy individuals, and 38 women with primary antiphospholipid syndrome (APS). Clinical and demographic characteristic of leprosy patients were collected, and serum samples, obtained from all participants, were kept frozen at - 20 degrees C. Antibodies were measured either by an in house-developed ELISA (aCL) or by a commercial ELISA (anti-beta(2)GPI).Results and Conclusions: Increased levels of aCL and anti-beta(2)GPI antibodies were found in leprosy patients and in the APS group, however, in contrast to APS, the predominant isotype in leprosy was IgM. The frequency of aCL and anti-beta(2)GPI antibodies was significantly higher in leprosy patients than in healthy individuals (15.8% vs. 3.1%; p < 0.01; 46.2% vs. 9.4%, p < 0.01), respectively. The lepromatous form predominated among aCL positive leprosy patients (p < 0.01). There was no difference in aCL and anti-beta(2)GPI positivity between leprosy patients taking MDT and those completed MDT as cured. Furthermore the duration of discharged period (period between discharge from MDT and the realization of the study) had no effect on anti-beta(2)GPI positivity, and a slight increase in aCL positivity was observed in patients with longer follow up periods (p=0.04), suggesting that the presence of antiphospholipid antibodies (aPL) was not a transient phenomenon. Although aPL in leprosy were frequent and beta(2)GPI-dependent as those found in APS, IgM was the predominant isotype, and there was no association with thrombosis or other APS manifestations.
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spelling Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patientsLeprosyAnti-beta(2)-glycoprotein I antibodiesAntiphospholipid antibodiesAnticardiolipin antibodiesAntiphospholipid syndromeObjectives: To determine the prevalence of anticardiolipin (aCL) and anti-beta(2)-glycoprotein I (anti-beta(2)GPI) antibodies in leprosy patients, during and after specific multidrug therapy (MDT), and to evaluate a possible association between these antibodies and some clinical characteristics of leprosy, including clinical forms, reactional episodes and treatment.Methods: The study included 158 leprosy patients, 129 gender-and-age matched healthy individuals, and 38 women with primary antiphospholipid syndrome (APS). Clinical and demographic characteristic of leprosy patients were collected, and serum samples, obtained from all participants, were kept frozen at - 20 degrees C. Antibodies were measured either by an in house-developed ELISA (aCL) or by a commercial ELISA (anti-beta(2)GPI).Results and Conclusions: Increased levels of aCL and anti-beta(2)GPI antibodies were found in leprosy patients and in the APS group, however, in contrast to APS, the predominant isotype in leprosy was IgM. The frequency of aCL and anti-beta(2)GPI antibodies was significantly higher in leprosy patients than in healthy individuals (15.8% vs. 3.1%; p < 0.01; 46.2% vs. 9.4%, p < 0.01), respectively. The lepromatous form predominated among aCL positive leprosy patients (p < 0.01). There was no difference in aCL and anti-beta(2)GPI positivity between leprosy patients taking MDT and those completed MDT as cured. Furthermore the duration of discharged period (period between discharge from MDT and the realization of the study) had no effect on anti-beta(2)GPI positivity, and a slight increase in aCL positivity was observed in patients with longer follow up periods (p=0.04), suggesting that the presence of antiphospholipid antibodies (aPL) was not a transient phenomenon. Although aPL in leprosy were frequent and beta(2)GPI-dependent as those found in APS, IgM was the predominant isotype, and there was no association with thrombosis or other APS manifestations.Univ Fed Amazonas, Div Rheumatol, Manaus, Amazonas, BrazilUniv Fed Sao Paulo, Div Rheumatol, Sao Paulo, BrazilUniv Fed Sao Paulo, Div Rheumatol, Sao Paulo, BrazilWeb of ScienceMedfarma-edicoes Medicas, LdaUniv Fed AmazonasUniversidade Federal de São Paulo (UNIFESP)Ribeiro, Sandra Lucia Euzebio [UNIFESP]Pereira, Helena Lúcia Alves [UNIFESP]Silva, Neusa Pereira da [UNIFESP]Souza, Alexandre Wagner Silva de [UNIFESP]Sato, Emilia Inoue [UNIFESP]2018-06-15T12:47:30Z2018-06-15T12:47:30Z2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion30-37application/pdfhttps://www.actareumatologica.pt/article_download.php?id=648Acta Reumatologica Portuguesa. Alges: Medfarma-edicoes Medicas, Lda, v. 36, n. 1, p. 30-37, 2011.WOS000288828700006.pdf0303-464Xhttps://repositorio.unifesp.br/handle/11600/42090WOS:000288828700006engActa Reumatologica Portuguesainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-09-16T13:54:37Zoai:repositorio.unifesp.br/:11600/42090Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-09-16T13:54:37Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
title Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
spellingShingle Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
Ribeiro, Sandra Lucia Euzebio [UNIFESP]
Leprosy
Anti-beta(2)-glycoprotein I antibodies
Antiphospholipid antibodies
Anticardiolipin antibodies
Antiphospholipid syndrome
title_short Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
title_full Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
title_fullStr Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
title_full_unstemmed Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
title_sort Anti-beta(2)-glycoprotein i antibodies are highly prevalent in a large number of Brazilian leprosy patients
author Ribeiro, Sandra Lucia Euzebio [UNIFESP]
author_facet Ribeiro, Sandra Lucia Euzebio [UNIFESP]
Pereira, Helena Lúcia Alves [UNIFESP]
Silva, Neusa Pereira da [UNIFESP]
Souza, Alexandre Wagner Silva de [UNIFESP]
Sato, Emilia Inoue [UNIFESP]
author_role author
author2 Pereira, Helena Lúcia Alves [UNIFESP]
Silva, Neusa Pereira da [UNIFESP]
Souza, Alexandre Wagner Silva de [UNIFESP]
Sato, Emilia Inoue [UNIFESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Univ Fed Amazonas
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ribeiro, Sandra Lucia Euzebio [UNIFESP]
Pereira, Helena Lúcia Alves [UNIFESP]
Silva, Neusa Pereira da [UNIFESP]
Souza, Alexandre Wagner Silva de [UNIFESP]
Sato, Emilia Inoue [UNIFESP]
dc.subject.por.fl_str_mv Leprosy
Anti-beta(2)-glycoprotein I antibodies
Antiphospholipid antibodies
Anticardiolipin antibodies
Antiphospholipid syndrome
topic Leprosy
Anti-beta(2)-glycoprotein I antibodies
Antiphospholipid antibodies
Anticardiolipin antibodies
Antiphospholipid syndrome
description Objectives: To determine the prevalence of anticardiolipin (aCL) and anti-beta(2)-glycoprotein I (anti-beta(2)GPI) antibodies in leprosy patients, during and after specific multidrug therapy (MDT), and to evaluate a possible association between these antibodies and some clinical characteristics of leprosy, including clinical forms, reactional episodes and treatment.Methods: The study included 158 leprosy patients, 129 gender-and-age matched healthy individuals, and 38 women with primary antiphospholipid syndrome (APS). Clinical and demographic characteristic of leprosy patients were collected, and serum samples, obtained from all participants, were kept frozen at - 20 degrees C. Antibodies were measured either by an in house-developed ELISA (aCL) or by a commercial ELISA (anti-beta(2)GPI).Results and Conclusions: Increased levels of aCL and anti-beta(2)GPI antibodies were found in leprosy patients and in the APS group, however, in contrast to APS, the predominant isotype in leprosy was IgM. The frequency of aCL and anti-beta(2)GPI antibodies was significantly higher in leprosy patients than in healthy individuals (15.8% vs. 3.1%; p < 0.01; 46.2% vs. 9.4%, p < 0.01), respectively. The lepromatous form predominated among aCL positive leprosy patients (p < 0.01). There was no difference in aCL and anti-beta(2)GPI positivity between leprosy patients taking MDT and those completed MDT as cured. Furthermore the duration of discharged period (period between discharge from MDT and the realization of the study) had no effect on anti-beta(2)GPI positivity, and a slight increase in aCL positivity was observed in patients with longer follow up periods (p=0.04), suggesting that the presence of antiphospholipid antibodies (aPL) was not a transient phenomenon. Although aPL in leprosy were frequent and beta(2)GPI-dependent as those found in APS, IgM was the predominant isotype, and there was no association with thrombosis or other APS manifestations.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01
2018-06-15T12:47:30Z
2018-06-15T12:47:30Z
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 https://www.actareumatologica.pt/article_download.php?id=648
Acta Reumatologica Portuguesa. Alges: Medfarma-edicoes Medicas, Lda, v. 36, n. 1, p. 30-37, 2011.
WOS000288828700006.pdf
0303-464X
https://repositorio.unifesp.br/handle/11600/42090
WOS:000288828700006
url https://www.actareumatologica.pt/article_download.php?id=648
https://repositorio.unifesp.br/handle/11600/42090
identifier_str_mv Acta Reumatologica Portuguesa. Alges: Medfarma-edicoes Medicas, Lda, v. 36, n. 1, p. 30-37, 2011.
WOS000288828700006.pdf
0303-464X
WOS:000288828700006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Acta Reumatologica Portuguesa
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 30-37
application/pdf
dc.publisher.none.fl_str_mv Medfarma-edicoes Medicas, Lda
publisher.none.fl_str_mv Medfarma-edicoes Medicas, Lda
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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