Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients

Detalhes bibliográficos
Autor(a) principal: Guarda, Caroline Conceição da
Data de Publicação: 2019
Outros Autores: Mattos, Paulo Sérgio de Morais da Silveira, Yahouédéhou, Sètondji C. M. A., Santiago, Rayra Pereira, Aleluia, Milena Magalhães, Figueiredo, Camylla Villas Boas, Fiuza, Luciana Magalhaes, Carvalho, Suellen Pinheiro, Oliveira, Rodrigo Mota de, Nascimento, Valma Maria Lopes, Luz, Nívea Farias, Borges, Valéria de Matos, Andrade, Bruno de Bezerril, Gonçalves, Marilda de Souza
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/37051
Resumo: Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.
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spelling Guarda, Caroline Conceição daMattos, Paulo Sérgio de Morais da SilveiraYahouédéhou, Sètondji C. M. A.Santiago, Rayra PereiraAleluia, Milena MagalhãesFigueiredo, Camylla Villas BoasFiuza, Luciana MagalhaesCarvalho, Suellen PinheiroOliveira, Rodrigo Mota deNascimento, Valma Maria LopesLuz, Nívea FariasBorges, Valéria de MatosAndrade, Bruno de BezerrilGonçalves, Marilda de Souza2019-11-14T12:49:49Z2019-11-14T12:49:49Z2019GUARDA, Caroline Conceição da et al. Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients. Scientific Reports, v. 9, p. 1-11, 2019.2045-2322https://www.arca.fiocruz.br/handle/icict/3705110.1038/s41598-019-51339-xengNature ResearchAnemia falciformeHidroxiureiaTratamentoHumanosAnemia, Sickle CellHydroxyureaTreatmentHumansHydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patientsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleFundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil / Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Inflamação e Biomarcadores. Salvador, BA, Brasil / Multinational Organization Network Sponsoring Translational and Epidemiological Research Initiative. Salvador, BA, Brazil / Faculdade de Tecnologia e Ciências. Curso de Medicina. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Fundação de Hematologia e Hemoterapia do Estado da Bahia. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Inflamação e Biomarcadores. Salvador, BA, Brasil / Multinational Organization Network Sponsoring Translational and Epidemiological Research Initiative. Salvador, BA, Brazil / Faculdade de Tecnologia e Ciências. Curso de Medicina. Salvador, BA, Brasil.Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil / Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Inflamação e Biomarcadores. Salvador, BA, Brasil / Multinational Organization Network Sponsoring Translational and Epidemiological Research Initiative. Salvador, BA, Brazil / Faculdade de Tecnologia e Ciências. Curso de Medicina. Salvador, BA, Brasil.Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil / Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Inflamação e Biomarcadores. Salvador, BA, Brasil / Multinational Organization Network Sponsoring Translational and Epidemiological Research Initiative. Salvador, BA, Brazil / Faculdade de Tecnologia e Ciências. Curso de Medicina. Salvador, BA, Brasil / Universidade Salvador. Laureate Universities. Salvador, BA, Brasil / Escola Bahiana de Medicina e Saúde Pública. Salvador, BA, Brasil.Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.Sickle cell anemia (SCA) is a hemolytic disease in which vaso-occlusion is an important pathophysiological mechanism. The treatment is based on hydroxyurea (HU), which decreases leukocyte counts and increases fetal hemoglobin synthesis. Different cell types are thought to contribute to vaso-occlusion. Nevertheless, the role of monocytes subsets remains unclear. We investigated frequencies of monocytes subsets in blood and their response to HU therapy, testing their ability to express pro-inflammatory molecules and tissue factor (TF). We identified major changes in monocyte subsets, with classical monocytes (CD14++CD16-) appearing highly frequent in who were not taking HU, whereas those with patrolling phenotype (CD14dimCD16+) were enriched in individuals undergoing therapy. Additionally, HU decreased the production of TNF-α, IL1-β, IL-6, IL-8 as well as TF by the LPS-activated monocytes. Likewise, frequency of TF-expressing monocytes is increased in patients with previous vaso-occlusion. Moreover, activated monocytes expressing TF produced several pro-inflammatory cytokines simultaneously. Such polyfunctional capacity was dramatically dampened by HU therapy. The frequency of classical monocytes subset was positively correlated with percentage cytokine producing cells upon LPS stimulation. These findings suggest that classical monocytes are the subset responsible for multiple pro-inflammatory cytokine production and possibly drive inflammation and vaso-occlusion in SCA which is damped by HU.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/37051/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALGuarda, C.C. Hydroxyuera....pdfGuarda, C.C. Hydroxyuera....pdfapplication/pdf3656637https://www.arca.fiocruz.br/bitstream/icict/37051/2/Guarda%2c%20C.C.%20Hydroxyuera....pdf14aab9fd62e1f2949b605d6f5956c6e4MD52TEXTGuarda, C.C. Hydroxyuera....pdf.txtGuarda, C.C. 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dc.title.pt_BR.fl_str_mv Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
title Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
spellingShingle Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
Guarda, Caroline Conceição da
Anemia falciforme
Hidroxiureia
Tratamento
Humanos
Anemia, Sickle Cell
Hydroxyurea
Treatment
Humans
title_short Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
title_full Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
title_fullStr Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
title_full_unstemmed Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
title_sort Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
author Guarda, Caroline Conceição da
author_facet Guarda, Caroline Conceição da
Mattos, Paulo Sérgio de Morais da Silveira
Yahouédéhou, Sètondji C. M. A.
Santiago, Rayra Pereira
Aleluia, Milena Magalhães
Figueiredo, Camylla Villas Boas
Fiuza, Luciana Magalhaes
Carvalho, Suellen Pinheiro
Oliveira, Rodrigo Mota de
Nascimento, Valma Maria Lopes
Luz, Nívea Farias
Borges, Valéria de Matos
Andrade, Bruno de Bezerril
Gonçalves, Marilda de Souza
author_role author
author2 Mattos, Paulo Sérgio de Morais da Silveira
Yahouédéhou, Sètondji C. M. A.
Santiago, Rayra Pereira
Aleluia, Milena Magalhães
Figueiredo, Camylla Villas Boas
Fiuza, Luciana Magalhaes
Carvalho, Suellen Pinheiro
Oliveira, Rodrigo Mota de
Nascimento, Valma Maria Lopes
Luz, Nívea Farias
Borges, Valéria de Matos
Andrade, Bruno de Bezerril
Gonçalves, Marilda de Souza
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Guarda, Caroline Conceição da
Mattos, Paulo Sérgio de Morais da Silveira
Yahouédéhou, Sètondji C. M. A.
Santiago, Rayra Pereira
Aleluia, Milena Magalhães
Figueiredo, Camylla Villas Boas
Fiuza, Luciana Magalhaes
Carvalho, Suellen Pinheiro
Oliveira, Rodrigo Mota de
Nascimento, Valma Maria Lopes
Luz, Nívea Farias
Borges, Valéria de Matos
Andrade, Bruno de Bezerril
Gonçalves, Marilda de Souza
dc.subject.other.pt_BR.fl_str_mv Anemia falciforme
Hidroxiureia
Tratamento
Humanos
topic Anemia falciforme
Hidroxiureia
Tratamento
Humanos
Anemia, Sickle Cell
Hydroxyurea
Treatment
Humans
dc.subject.en.pt_BR.fl_str_mv Anemia, Sickle Cell
Hydroxyurea
Treatment
Humans
description Fundação Oswaldo Cruz. Instituto Gonçalo Moniz. Laboratório de Investigação em Genética e Hematologia Translacional. Salvador, BA, Brasil / Universidade Federal da Bahia. Faculdade de Medicina da Bahia. Salvador, BA, Brasil.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-11-14T12:49:49Z
dc.date.available.fl_str_mv 2019-11-14T12:49:49Z
dc.date.issued.fl_str_mv 2019
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.citation.fl_str_mv GUARDA, Caroline Conceição da et al. Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients. Scientific Reports, v. 9, p. 1-11, 2019.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/37051
dc.identifier.issn.pt_BR.fl_str_mv 2045-2322
dc.identifier.doi.none.fl_str_mv 10.1038/s41598-019-51339-x
identifier_str_mv GUARDA, Caroline Conceição da et al. Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients. Scientific Reports, v. 9, p. 1-11, 2019.
2045-2322
10.1038/s41598-019-51339-x
url https://www.arca.fiocruz.br/handle/icict/37051
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