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Cytometry B Clin Cytom ; 96(6): 490-495, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-30828998

RESUMEN

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. © 2019 International Clinical Cytometry Society.


Asunto(s)
Carcinoma Hepatocelular/metabolismo , Colangiocarcinoma/metabolismo , Células Dendríticas/metabolismo , Neoplasias Hepáticas/metabolismo , Monocitos/metabolismo , Células Mieloides/metabolismo , Receptores de IgE/metabolismo , Carcinoma Hepatocelular/patología , Carcinoma Hepatocelular/cirugía , Colangiocarcinoma/patología , Colangiocarcinoma/cirugía , Células Dendríticas/patología , Femenino , Citometría de Flujo , Humanos , Neoplasias Hepáticas/patología , Neoplasias Hepáticas/cirugía , Masculino , Persona de Mediana Edad , Monocitos/patología , Células Mieloides/patología , Fenotipo , Receptores de IgE/sangre
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