CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , |
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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Jornal Brasileiro de Nefrologia |
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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 |
_version_ |
1752122065036509184 |