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CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation

The TRANSPEG study was a prospective study to assess the efficacy of antiviral therapy in patients with a recurrent hepatitis C virus (HCV) after liver transplantation. The influence of regulatory T-cells (Tregs) on the response to antiviral therapy was analyzed. Patients were considered as a functi...

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Autores principales: Fabien, Stenard, Olivier, Morales, Khaldoun, Ghazal, Vivian, Viallon, Lynda, Aoudjehane, Laurissa, Ouaguia, Gautier, Goormachtigh, Yvon, Calmus, Nadira, Delhem, Filomena, Conti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915765/
https://www.ncbi.nlm.nih.gov/pubmed/24575405
http://dx.doi.org/10.1155/2014/290878
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author Fabien, Stenard
Olivier, Morales
Khaldoun, Ghazal
Vivian, Viallon
Lynda, Aoudjehane
Laurissa, Ouaguia
Gautier, Goormachtigh
Yvon, Calmus
Nadira, Delhem
Filomena, Conti
author_facet Fabien, Stenard
Olivier, Morales
Khaldoun, Ghazal
Vivian, Viallon
Lynda, Aoudjehane
Laurissa, Ouaguia
Gautier, Goormachtigh
Yvon, Calmus
Nadira, Delhem
Filomena, Conti
author_sort Fabien, Stenard
collection PubMed
description The TRANSPEG study was a prospective study to assess the efficacy of antiviral therapy in patients with a recurrent hepatitis C virus (HCV) after liver transplantation. The influence of regulatory T-cells (Tregs) on the response to antiviral therapy was analyzed. Patients were considered as a function of their sustained virological response (SVR) at 18 months after treatment initiation. A transcriptomic analysis was performed to assess Treg markers (Tr1 and FoxP3(+)) in serum, PBMC, and liver biopsies. 100 patients had been included in the TRANSPEG study. Data from 27 of these patients were available. The results showed that the expression of CD49b (a predominant marker of Tr1) before the introduction of antiviral therapy was significantly associated with SVR. Responders displayed lower serum levels of CD49b than nonresponders (P < 0.02). These findings were confirmed in PBMC and liver biopsies even if in a nonsignificant manner for the limited number of samples. The assessment of CD49b levels is thus predictive of the response to antiviral therapy. This data suggests that CD49b may be a marker of the failure of the immune response and antiviral therapy during HCV recurrence. The assessment of CD49b could help to select patients who require earlier and more intensive antiviral therapy.
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spelling pubmed-39157652014-02-26 CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation Fabien, Stenard Olivier, Morales Khaldoun, Ghazal Vivian, Viallon Lynda, Aoudjehane Laurissa, Ouaguia Gautier, Goormachtigh Yvon, Calmus Nadira, Delhem Filomena, Conti Biomed Res Int Research Article The TRANSPEG study was a prospective study to assess the efficacy of antiviral therapy in patients with a recurrent hepatitis C virus (HCV) after liver transplantation. The influence of regulatory T-cells (Tregs) on the response to antiviral therapy was analyzed. Patients were considered as a function of their sustained virological response (SVR) at 18 months after treatment initiation. A transcriptomic analysis was performed to assess Treg markers (Tr1 and FoxP3(+)) in serum, PBMC, and liver biopsies. 100 patients had been included in the TRANSPEG study. Data from 27 of these patients were available. The results showed that the expression of CD49b (a predominant marker of Tr1) before the introduction of antiviral therapy was significantly associated with SVR. Responders displayed lower serum levels of CD49b than nonresponders (P < 0.02). These findings were confirmed in PBMC and liver biopsies even if in a nonsignificant manner for the limited number of samples. The assessment of CD49b levels is thus predictive of the response to antiviral therapy. This data suggests that CD49b may be a marker of the failure of the immune response and antiviral therapy during HCV recurrence. The assessment of CD49b could help to select patients who require earlier and more intensive antiviral therapy. Hindawi Publishing Corporation 2014 2014-01-19 /pmc/articles/PMC3915765/ /pubmed/24575405 http://dx.doi.org/10.1155/2014/290878 Text en Copyright © 2014 Stenard Fabien et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fabien, Stenard
Olivier, Morales
Khaldoun, Ghazal
Vivian, Viallon
Lynda, Aoudjehane
Laurissa, Ouaguia
Gautier, Goormachtigh
Yvon, Calmus
Nadira, Delhem
Filomena, Conti
CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title_full CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title_fullStr CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title_full_unstemmed CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title_short CD49b, a Major Marker of Regulatory T-Cells Type 1, Predicts the Response to Antiviral Therapy of Recurrent Hepatitis C after Liver Transplantation
title_sort cd49b, a major marker of regulatory t-cells type 1, predicts the response to antiviral therapy of recurrent hepatitis c after liver transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915765/
https://www.ncbi.nlm.nih.gov/pubmed/24575405
http://dx.doi.org/10.1155/2014/290878
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