Neutrophil and monocyte function in patients with chronic Hepatitis C undergoing antiviral therapy with regimens containing protease inhibitors with and without Interferon
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- dc.contributor.author Gambato, Martinaca
- dc.contributor.author Caro-Pérez, Noeliaca
- dc.contributor.author González, Patriciaca
- dc.contributor.author Cañete Hidalgo, Nuriaca
- dc.contributor.author Mariño, Zoeca
- dc.contributor.author Lens, Sabelaca
- dc.contributor.author Bonacci, Martínca
- dc.contributor.author Bartres, Concepcióca
- dc.contributor.author Sánchez-Tapias, José-Maríaca
- dc.contributor.author Carrión Rodríguez, José Antonioca
- dc.contributor.author Forns, Xavierca
- dc.contributor.author Juan, Manelca
- dc.contributor.author Pérez-del-Pulgar, Sofíaca
- dc.contributor.author Londoño, María-Carlotaca
- dc.date.accessioned 2018-02-15T08:38:22Z
- dc.date.available 2018-02-15T08:38:22Z
- dc.date.issued 2016
- dc.description.abstract Real-life data showed an increased incidence of bacterial infections in patients with advanced liver disease receiving a protease inhibitor (PI)-containing antiviral regimen against hepatitis C (HCV). However, the causes of this event are unknown. We hypothesized that PIs might impair innate immune responses through the inhibition of proteases participating in the anti-bacterial functions of neutrophils and monocytes. The aims of the study were to assess phagocytic and oxidative burst capacity in neutrophils and monocytes obtained from patients receiving a PI containing-antiviral regimen, and to determine cytokine secretion after neutrophil stimulation with flagellin. Forty patients with chronic HCV (80% with cirrhosis) were enrolled in the study, 28 received triple therapy (Group A) with pegylated-interferon and ribavirin for 4 weeks followed by the addition of a PI (telaprevir, boceprevir or simeprevir), and 12 patients received an interferon-free regimen (Group B) with simeprevir and sofosbuvir. Phagocytosis and oxidative burst capacity were analyzed by flow cytometry at baseline, week 4, and week 8 of therapy. In neutrophils from Group A patients, oxidative burst rate and oxidative enzymatic activity per cell significantly decreased throughout the study period (p = 0.014 and p = 0.010, respectively). Pairwise comparisons showed a decrease between baseline and week 4 and 8 of therapy. No differences were observed after the introduction of the PI. The oxidative enzymatic activity per cell in monocytes significantly decrease during the study period (p = 0.042) due to a decrease from baseline to week 8 of therapy (p = 0.037) in patients from Group A. None of these findings were observed in Group B patients. Cytokine secretion did not significantly change during the study in both groups. In conclusion, our data suggest that the use interferon (rather than the PI) has a deleterious effect on neutrophil and monocyte phagocytic and oxidative burst capacity in this cohort of patients with HCV-related advanced liver fibrosis
- dc.format.mimetype application/pdf
- dc.identifier.citation Gambato M, Caro-Pérez N, González P, Cañete N, Mariño Z, Lens S. et al. Neutrophil and monocyte function in patients with chronic Hepatitis C undergoing antiviral therapy with regimens containing protease inhibitors with and without Interferon. PLoS One. 2016 Nov 18;11(11):e0166631. DOI: 10.1371/journal.pone.0166631
- dc.identifier.doi http://dx.doi.org/10.1371/journal.pone.0166631
- dc.identifier.issn 1932-6203
- dc.identifier.uri http://hdl.handle.net/10230/33914
- dc.language.iso eng
- dc.publisher Public Library of Science (PLoS)ca
- dc.relation.ispartof PLoS One. 2016 Nov 18;11(11):e0166631
- dc.rights Copyright: © 2016 Gambato et al. This is an open access article distributed under the terms of the https://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
- dc.rights.accessRights info:eu-repo/semantics/openAccess
- dc.subject.other Hepatitis C
- dc.subject.other Interferó
- dc.title Neutrophil and monocyte function in patients with chronic Hepatitis C undergoing antiviral therapy with regimens containing protease inhibitors with and without Interferonca
- dc.type info:eu-repo/semantics/article
- dc.type.version info:eu-repo/semantics/publishedVersion