Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients

Detalhes bibliográficos
Autor(a) principal: Martín-Sierra, Carmen
Data de Publicação: 2019
Outros Autores: Martins, Ricardo, Laranjeira, Paula, Abrantes, A. Margarida, Oliveira, R. Caetano, Tralhão, J. Guilherme, Botelho, M. Filomena, Furtado, Emanuel, Domingues, Rosário, Paiva, Artur
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/27221
Resumo: Background Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) represent the most common primary liver malignancies whose outcome is influenced by the immune response. Methods In this study, we have functionally characterized, by flow cytometry, circulating myeloid dendritic cells (mDCs) and FcεRI+ monocytes in a group of healthy individuals (n = 10) and in a group of patients with HCC (n = 19) and CCA (n = 8), at the time point of the surgical resection (T0) and once the patient had recovered from surgery (T1). Moreover, we proceeded to a more in depth phenotypic characterization of the FcεRI+ monocyte subpopulation. Results A significant decrease in the frequency of TNFα producing FcεRI+ monocytes and mDCs in HCC and CCA patients when compared to the group of healthy individuals was observed, and a close association between FcεRI+ monocytes and mDCs dysfunction was identified. In addition, the phenotypic characteristics of FcεRI+ monocytes from healthy individuals strongly suggest that this population drives to mDCs, which matches with the fact that both populations are functionally affected. Conclusions The frequency and the function of circulating mDCs and FcεRI+ monocytes are affected in both HCC and CCA patients, and FcεRI+ monocytes could represent those fated to become mDCs.
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spelling Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patientsMyeloid dendritic cellsMonocytesTNFαHepatocellular carcinomaCholangiocarcinomaBackground Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) represent the most common primary liver malignancies whose outcome is influenced by the immune response. Methods In this study, we have functionally characterized, by flow cytometry, circulating myeloid dendritic cells (mDCs) and FcεRI+ monocytes in a group of healthy individuals (n = 10) and in a group of patients with HCC (n = 19) and CCA (n = 8), at the time point of the surgical resection (T0) and once the patient had recovered from surgery (T1). Moreover, we proceeded to a more in depth phenotypic characterization of the FcεRI+ monocyte subpopulation. Results A significant decrease in the frequency of TNFα producing FcεRI+ monocytes and mDCs in HCC and CCA patients when compared to the group of healthy individuals was observed, and a close association between FcεRI+ monocytes and mDCs dysfunction was identified. In addition, the phenotypic characteristics of FcεRI+ monocytes from healthy individuals strongly suggest that this population drives to mDCs, which matches with the fact that both populations are functionally affected. Conclusions The frequency and the function of circulating mDCs and FcεRI+ monocytes are affected in both HCC and CCA patients, and FcεRI+ monocytes could represent those fated to become mDCs.2019-112019-11-01T00:00:00Z2020-11-30T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/10773/27221eng1552-494910.1002/cyto.b.21777Martín-Sierra, CarmenMartins, RicardoLaranjeira, PaulaAbrantes, A. MargaridaOliveira, R. CaetanoTralhão, J. GuilhermeBotelho, M. FilomenaFurtado, EmanuelDomingues, RosárioPaiva, Arturinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:52:45Zoai:ria.ua.pt:10773/27221Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:00:03.529004Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
title Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
spellingShingle Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
Martín-Sierra, Carmen
Myeloid dendritic cells
Monocytes
TNFα
Hepatocellular carcinoma
Cholangiocarcinoma
title_short Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
title_full Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
title_fullStr Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
title_full_unstemmed Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
title_sort Functional impairment of circulating FcεRI+ monocytes and myeloid dendritic cells in hepatocellular carcinoma and cholangiocarcinoma patients
author Martín-Sierra, Carmen
author_facet Martín-Sierra, Carmen
Martins, Ricardo
Laranjeira, Paula
Abrantes, A. Margarida
Oliveira, R. Caetano
Tralhão, J. Guilherme
Botelho, M. Filomena
Furtado, Emanuel
Domingues, Rosário
Paiva, Artur
author_role author
author2 Martins, Ricardo
Laranjeira, Paula
Abrantes, A. Margarida
Oliveira, R. Caetano
Tralhão, J. Guilherme
Botelho, M. Filomena
Furtado, Emanuel
Domingues, Rosário
Paiva, Artur
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Martín-Sierra, Carmen
Martins, Ricardo
Laranjeira, Paula
Abrantes, A. Margarida
Oliveira, R. Caetano
Tralhão, J. Guilherme
Botelho, M. Filomena
Furtado, Emanuel
Domingues, Rosário
Paiva, Artur
dc.subject.por.fl_str_mv Myeloid dendritic cells
Monocytes
TNFα
Hepatocellular carcinoma
Cholangiocarcinoma
topic Myeloid dendritic cells
Monocytes
TNFα
Hepatocellular carcinoma
Cholangiocarcinoma
description Background Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) represent the most common primary liver malignancies whose outcome is influenced by the immune response. Methods In this study, we have functionally characterized, by flow cytometry, circulating myeloid dendritic cells (mDCs) and FcεRI+ monocytes in a group of healthy individuals (n = 10) and in a group of patients with HCC (n = 19) and CCA (n = 8), at the time point of the surgical resection (T0) and once the patient had recovered from surgery (T1). Moreover, we proceeded to a more in depth phenotypic characterization of the FcεRI+ monocyte subpopulation. Results A significant decrease in the frequency of TNFα producing FcεRI+ monocytes and mDCs in HCC and CCA patients when compared to the group of healthy individuals was observed, and a close association between FcεRI+ monocytes and mDCs dysfunction was identified. In addition, the phenotypic characteristics of FcεRI+ monocytes from healthy individuals strongly suggest that this population drives to mDCs, which matches with the fact that both populations are functionally affected. Conclusions The frequency and the function of circulating mDCs and FcεRI+ monocytes are affected in both HCC and CCA patients, and FcεRI+ monocytes could represent those fated to become mDCs.
publishDate 2019
dc.date.none.fl_str_mv 2019-11
2019-11-01T00:00:00Z
2020-11-30T00:00:00Z
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url http://hdl.handle.net/10773/27221
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1552-4949
10.1002/cyto.b.21777
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