CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)

Detalhes bibliográficos
Autor(a) principal: Pereira,Ester Miranda
Data de Publicação: 2018
Outros Autores: Silva,Adalberto Socorro da, Silva,Raimundo Nonato da, Monte Neto,José Tiburcio, Nascimento,Fernando F. do, Sousa,Jackeline L. M., Costa Filho,Henrique César Saraiva de Arêa Leão, Sales Filho,Herton Luiz Alves, Labilloy,Anatalia, Monte,Semiramis Jamil Hadad do
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal Brasileiro de Nefrologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018000400333
Resumo: ABSTRACT Introduction: Fabry disease (FD) is a disorder caused by mutations in the gene encoding for lysosomal enzyme α-galactosidase A (α-GAL). Reduced α-GAL activity leads to progressive accumulation of globotriaosylceramide (Gb3), also known as CD77. The recent report of increased expression of CD77 in blood cells of patients with FD indicated that this molecule can be used as a potential marker for monitoring enzyme replacement therapy (ERT). Objective: The purpose of this study was to evaluate the CD77 levels throughout ERT in FD patients (V269M mutation). Methods: We evaluated the fluctuations in PBMC (peripheral blood mononuclear cell) membrane CD77 expression in FD patients undergoing ERT and correlated these levels with those observed in different cell types. Results: A greater CD77 expression was found in phagocytes of patients compared to controls at baseline. Interestingly, the variability in CD77 levels is larger in patients at baseline (340 - 1619 MIF) and after 12 months of ERT (240 - 530 MIF) compared with the control group (131 - 331 MFI). Furthermore, by analyzing the levels of CD77 in phagocytes from patients throughout ERT, we found a constant decrease in CD77 levels. Conclusion: The increased CD77 levels in the phagocytes of Fabry carriers together with the decrease in CD77 levels throughout ERT suggest that measuring CD77 levels in phagocytes is a promising tool for monitoring the response to ERT in FD.
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spelling CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)Fabry DiseaseEnzyme Replacement TherapyPhagocytesABSTRACT Introduction: Fabry disease (FD) is a disorder caused by mutations in the gene encoding for lysosomal enzyme α-galactosidase A (α-GAL). Reduced α-GAL activity leads to progressive accumulation of globotriaosylceramide (Gb3), also known as CD77. The recent report of increased expression of CD77 in blood cells of patients with FD indicated that this molecule can be used as a potential marker for monitoring enzyme replacement therapy (ERT). Objective: The purpose of this study was to evaluate the CD77 levels throughout ERT in FD patients (V269M mutation). Methods: We evaluated the fluctuations in PBMC (peripheral blood mononuclear cell) membrane CD77 expression in FD patients undergoing ERT and correlated these levels with those observed in different cell types. Results: A greater CD77 expression was found in phagocytes of patients compared to controls at baseline. Interestingly, the variability in CD77 levels is larger in patients at baseline (340 - 1619 MIF) and after 12 months of ERT (240 - 530 MIF) compared with the control group (131 - 331 MFI). Furthermore, by analyzing the levels of CD77 in phagocytes from patients throughout ERT, we found a constant decrease in CD77 levels. Conclusion: The increased CD77 levels in the phagocytes of Fabry carriers together with the decrease in CD77 levels throughout ERT suggest that measuring CD77 levels in phagocytes is a promising tool for monitoring the response to ERT in FD.Sociedade Brasileira de Nefrologia2018-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018000400333Brazilian Journal of Nephrology v.40 n.4 2018reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.1590/2175-8239-jbn-3910info:eu-repo/semantics/openAccessPereira,Ester MirandaSilva,Adalberto Socorro daSilva,Raimundo Nonato daMonte Neto,José TiburcioNascimento,Fernando F. doSousa,Jackeline L. M.Costa Filho,Henrique César Saraiva de Arêa LeãoSales Filho,Herton Luiz AlvesLabilloy,AnataliaMonte,Semiramis Jamil Hadad doeng2019-02-05T00:00:00Zoai:scielo:S0101-28002018000400333Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2019-02-05T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false
dc.title.none.fl_str_mv CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
title CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
spellingShingle CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
Pereira,Ester Miranda
Fabry Disease
Enzyme Replacement Therapy
Phagocytes
title_short CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
title_full CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
title_fullStr CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
title_full_unstemmed CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
title_sort CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
author Pereira,Ester Miranda
author_facet Pereira,Ester Miranda
Silva,Adalberto Socorro da
Silva,Raimundo Nonato da
Monte Neto,José Tiburcio
Nascimento,Fernando F. do
Sousa,Jackeline L. M.
Costa Filho,Henrique César Saraiva de Arêa Leão
Sales Filho,Herton Luiz Alves
Labilloy,Anatalia
Monte,Semiramis Jamil Hadad do
author_role author
author2 Silva,Adalberto Socorro da
Silva,Raimundo Nonato da
Monte Neto,José Tiburcio
Nascimento,Fernando F. do
Sousa,Jackeline L. M.
Costa Filho,Henrique César Saraiva de Arêa Leão
Sales Filho,Herton Luiz Alves
Labilloy,Anatalia
Monte,Semiramis Jamil Hadad do
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pereira,Ester Miranda
Silva,Adalberto Socorro da
Silva,Raimundo Nonato da
Monte Neto,José Tiburcio
Nascimento,Fernando F. do
Sousa,Jackeline L. M.
Costa Filho,Henrique César Saraiva de Arêa Leão
Sales Filho,Herton Luiz Alves
Labilloy,Anatalia
Monte,Semiramis Jamil Hadad do
dc.subject.por.fl_str_mv Fabry Disease
Enzyme Replacement Therapy
Phagocytes
topic Fabry Disease
Enzyme Replacement Therapy
Phagocytes
description ABSTRACT Introduction: Fabry disease (FD) is a disorder caused by mutations in the gene encoding for lysosomal enzyme α-galactosidase A (α-GAL). Reduced α-GAL activity leads to progressive accumulation of globotriaosylceramide (Gb3), also known as CD77. The recent report of increased expression of CD77 in blood cells of patients with FD indicated that this molecule can be used as a potential marker for monitoring enzyme replacement therapy (ERT). Objective: The purpose of this study was to evaluate the CD77 levels throughout ERT in FD patients (V269M mutation). Methods: We evaluated the fluctuations in PBMC (peripheral blood mononuclear cell) membrane CD77 expression in FD patients undergoing ERT and correlated these levels with those observed in different cell types. Results: A greater CD77 expression was found in phagocytes of patients compared to controls at baseline. Interestingly, the variability in CD77 levels is larger in patients at baseline (340 - 1619 MIF) and after 12 months of ERT (240 - 530 MIF) compared with the control group (131 - 331 MFI). Furthermore, by analyzing the levels of CD77 in phagocytes from patients throughout ERT, we found a constant decrease in CD77 levels. Conclusion: The increased CD77 levels in the phagocytes of Fabry carriers together with the decrease in CD77 levels throughout ERT suggest that measuring CD77 levels in phagocytes is a promising tool for monitoring the response to ERT in FD.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018000400333
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002018000400333
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2175-8239-jbn-3910
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 Sociedade Brasileira de Nefrologia
publisher.none.fl_str_mv Sociedade Brasileira de Nefrologia
dc.source.none.fl_str_mv Brazilian Journal of Nephrology v.40 n.4 2018
reponame:Jornal Brasileiro de Nefrologia
instname:Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
instname_str Sociedade Brasileira de Nefrologia (SBN)
instacron_str SBN
institution SBN
reponame_str Jornal Brasileiro de Nefrologia
collection Jornal Brasileiro de Nefrologia
repository.name.fl_str_mv Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)
repository.mail.fl_str_mv ||jbn@sbn.org.br
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