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Viral and immune factors associated with successful treatment withdrawal in HBeAg-negative chronic hepatitis B patients

Factors associated with a successful outcome upon nucleos(t)ide analogue (NA) treatment withdrawal in HBeAg-negative chronic hepatitis B (CHB) patients have yet to be clarified. The objective of this study was to analyse the HBV-specific T cell response, in parallel with peripheral and intrahepatic...

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Published in:Journal of hepatology 2021-05, Vol.74 (5), p.1064-1074
Main Authors: García-López, Mireia, Lens, Sabela, Pallett, Laura J., Testoni, Barbara, Rodríguez-Tajes, Sergio, Mariño, Zoe, Bartres, Concepción, García-Pras, Ester, Leonel, Thais, Perpiñán, Elena, Lozano, Juan José, Rodríguez-Frías, Francisco, Koutsoudakis, George, Zoulim, Fabien, Maini, Mala K., Forns, Xavier, Pérez-del-Pulgar, Sofía
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cited_by cdi_FETCH-LOGICAL-c517t-f936dd249cb93107cc70e55a270f36771fb52c1a3d4811c2da0b88b2b0557a523
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container_end_page 1074
container_issue 5
container_start_page 1064
container_title Journal of hepatology
container_volume 74
creator García-López, Mireia
Lens, Sabela
Pallett, Laura J.
Testoni, Barbara
Rodríguez-Tajes, Sergio
Mariño, Zoe
Bartres, Concepción
García-Pras, Ester
Leonel, Thais
Perpiñán, Elena
Lozano, Juan José
Rodríguez-Frías, Francisco
Koutsoudakis, George
Zoulim, Fabien
Maini, Mala K.
Forns, Xavier
Pérez-del-Pulgar, Sofía
description Factors associated with a successful outcome upon nucleos(t)ide analogue (NA) treatment withdrawal in HBeAg-negative chronic hepatitis B (CHB) patients have yet to be clarified. The objective of this study was to analyse the HBV-specific T cell response, in parallel with peripheral and intrahepatic viral parameters, in patients undergoing NA discontinuation. Twenty-seven patients without cirrhosis with HBeAg-negative CHB with complete viral suppression (>3 years) were studied prospectively. Intrahepatic HBV-DNA (iHBV-DNA), intrahepatic HBV-RNA (iHBV-RNA), and covalently closed circular DNA (cccDNA) were quantified at baseline. Additionally, serum markers (HBV-DNA, HBsAg, HBV core-related antigen [HBcrAg] and HBV-RNA) and HBV-specific T cell responses were analysed at baseline and longitudinally throughout follow-up. After a median follow-up of 34 months, 22/27 patients (82%) remained off-therapy, of whom 8 patients (30% of the total cohort) lost HBsAg. Baseline HBsAg significantly correlated with iHBV-DNA and iHBV-RNA, and these parameters were lower in patients who lost HBsAg. All patients had similar levels of detectable cccDNA regardless of their clinical outcome. Patients achieving functional cure had baseline HBsAg levels ≤1,000 IU/ml. Similarly, an increased frequency of functional HBV-specific CD8+ T cells at baseline was associated with sustained viral control off treatment. These HBV-specific T cell responses persisted, but did not increase, after treatment withdrawal. A similar, but not statistically significant trend, was observed for HBV-specific CD4+ T cell responses. Decreased cccDNA transcription and low HBsAg levels are associated with HBsAg loss upon NA discontinuation in patients with HBeAg-negative CHB. The presence of functional HBV-specific T cells at baseline are associated with a successful outcome after treatment withdrawal. Nucleos(t)ide analogue therapy can be discontinued in a high proportion of chronic hepatitis B patients without cirrhosis. The strength of HBV-specific immune T cell responses may contribute to successful viral control after antiviral treatment interruption. Our comprehensive study provides in-depth data on virological and immunological factors than can help guide individualised therapy in patients with chronic hepatitis B. [Display omitted] •Stopping NA is feasible in a high proportion of HBeAg-negative CHB patients.•Low baseline HBsAg titres identify patients who will achieve functional cure.•Reduced cccDNA ac
doi_str_mv 10.1016/j.jhep.2020.11.043
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The objective of this study was to analyse the HBV-specific T cell response, in parallel with peripheral and intrahepatic viral parameters, in patients undergoing NA discontinuation. Twenty-seven patients without cirrhosis with HBeAg-negative CHB with complete viral suppression (&gt;3 years) were studied prospectively. Intrahepatic HBV-DNA (iHBV-DNA), intrahepatic HBV-RNA (iHBV-RNA), and covalently closed circular DNA (cccDNA) were quantified at baseline. Additionally, serum markers (HBV-DNA, HBsAg, HBV core-related antigen [HBcrAg] and HBV-RNA) and HBV-specific T cell responses were analysed at baseline and longitudinally throughout follow-up. After a median follow-up of 34 months, 22/27 patients (82%) remained off-therapy, of whom 8 patients (30% of the total cohort) lost HBsAg. Baseline HBsAg significantly correlated with iHBV-DNA and iHBV-RNA, and these parameters were lower in patients who lost HBsAg. All patients had similar levels of detectable cccDNA regardless of their clinical outcome. Patients achieving functional cure had baseline HBsAg levels ≤1,000 IU/ml. Similarly, an increased frequency of functional HBV-specific CD8+ T cells at baseline was associated with sustained viral control off treatment. These HBV-specific T cell responses persisted, but did not increase, after treatment withdrawal. A similar, but not statistically significant trend, was observed for HBV-specific CD4+ T cell responses. Decreased cccDNA transcription and low HBsAg levels are associated with HBsAg loss upon NA discontinuation in patients with HBeAg-negative CHB. The presence of functional HBV-specific T cells at baseline are associated with a successful outcome after treatment withdrawal. Nucleos(t)ide analogue therapy can be discontinued in a high proportion of chronic hepatitis B patients without cirrhosis. The strength of HBV-specific immune T cell responses may contribute to successful viral control after antiviral treatment interruption. Our comprehensive study provides in-depth data on virological and immunological factors than can help guide individualised therapy in patients with chronic hepatitis B. [Display omitted] •Stopping NA is feasible in a high proportion of HBeAg-negative CHB patients.•Low baseline HBsAg titres identify patients who will achieve functional cure.•Reduced cccDNA activity is associated with HBsAg loss after NA discontinuation.•HBV-specific T cell functionality may influence patient outcome upon NA withdrawal.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2020.11.043</identifier><identifier>PMID: 33278456</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Antiviral Agents - therapeutic use ; Antiviral therapy discontinuation ; Biomarkers - blood ; CD4 antigen ; CD8 antigen ; Chronic hepatitis B ; Circular DNA ; Circular RNA ; Cirrhosis ; Covalently closed circular DNA ; DNA, Circular - isolation &amp; purification ; DNA, Viral - isolation &amp; purification ; Female ; HBcrAg ; HBsAg ; HBV-RNA ; HBV-Specific T cells ; Hepatitis B ; Hepatitis B Antigens - analysis ; Hepatitis B Antigens - isolation &amp; purification ; Hepatitis B e antigen ; Hepatitis B surface antigen ; Hepatitis B Surface Antigens - analysis ; Hepatitis B virus ; Hepatitis B virus - genetics ; Hepatitis B virus - isolation &amp; purification ; Hepatitis B, Chronic - blood ; Hepatitis B, Chronic - diagnosis ; Human health and pathology ; Humans ; Hépatology and Gastroenterology ; Immune response ; Immunity, Cellular - drug effects ; Immunity, Cellular - immunology ; Interferon ; Life Sciences ; Liver - pathology ; Liver - virology ; Liver cirrhosis ; Lymphocytes ; Lymphocytes T ; Male ; Middle Aged ; Nucleos(t)ide analogue ; Nucleosides - therapeutic use ; Patient Care Planning ; Patients ; Ribonucleic acid ; RNA ; Statistical analysis ; Transcription ; Withholding Treatment - statistics &amp; numerical data</subject><ispartof>Journal of hepatology, 2021-05, Vol.74 (5), p.1064-1074</ispartof><rights>2020 European Association for the Study of the Liver</rights><rights>Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. May 2021</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2020 European Association for the Study of the Liver. 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The objective of this study was to analyse the HBV-specific T cell response, in parallel with peripheral and intrahepatic viral parameters, in patients undergoing NA discontinuation. Twenty-seven patients without cirrhosis with HBeAg-negative CHB with complete viral suppression (&gt;3 years) were studied prospectively. Intrahepatic HBV-DNA (iHBV-DNA), intrahepatic HBV-RNA (iHBV-RNA), and covalently closed circular DNA (cccDNA) were quantified at baseline. Additionally, serum markers (HBV-DNA, HBsAg, HBV core-related antigen [HBcrAg] and HBV-RNA) and HBV-specific T cell responses were analysed at baseline and longitudinally throughout follow-up. After a median follow-up of 34 months, 22/27 patients (82%) remained off-therapy, of whom 8 patients (30% of the total cohort) lost HBsAg. Baseline HBsAg significantly correlated with iHBV-DNA and iHBV-RNA, and these parameters were lower in patients who lost HBsAg. All patients had similar levels of detectable cccDNA regardless of their clinical outcome. Patients achieving functional cure had baseline HBsAg levels ≤1,000 IU/ml. Similarly, an increased frequency of functional HBV-specific CD8+ T cells at baseline was associated with sustained viral control off treatment. These HBV-specific T cell responses persisted, but did not increase, after treatment withdrawal. A similar, but not statistically significant trend, was observed for HBV-specific CD4+ T cell responses. Decreased cccDNA transcription and low HBsAg levels are associated with HBsAg loss upon NA discontinuation in patients with HBeAg-negative CHB. The presence of functional HBV-specific T cells at baseline are associated with a successful outcome after treatment withdrawal. Nucleos(t)ide analogue therapy can be discontinued in a high proportion of chronic hepatitis B patients without cirrhosis. The strength of HBV-specific immune T cell responses may contribute to successful viral control after antiviral treatment interruption. Our comprehensive study provides in-depth data on virological and immunological factors than can help guide individualised therapy in patients with chronic hepatitis B. [Display omitted] •Stopping NA is feasible in a high proportion of HBeAg-negative CHB patients.•Low baseline HBsAg titres identify patients who will achieve functional cure.•Reduced cccDNA activity is associated with HBsAg loss after NA discontinuation.•HBV-specific T cell functionality may influence patient outcome upon NA withdrawal.</description><subject>Antiviral Agents - therapeutic use</subject><subject>Antiviral therapy discontinuation</subject><subject>Biomarkers - blood</subject><subject>CD4 antigen</subject><subject>CD8 antigen</subject><subject>Chronic hepatitis B</subject><subject>Circular DNA</subject><subject>Circular RNA</subject><subject>Cirrhosis</subject><subject>Covalently closed circular DNA</subject><subject>DNA, Circular - isolation &amp; purification</subject><subject>DNA, Viral - isolation &amp; purification</subject><subject>Female</subject><subject>HBcrAg</subject><subject>HBsAg</subject><subject>HBV-RNA</subject><subject>HBV-Specific T cells</subject><subject>Hepatitis B</subject><subject>Hepatitis B Antigens - analysis</subject><subject>Hepatitis B Antigens - isolation &amp; 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numerical data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García-López, Mireia</creatorcontrib><creatorcontrib>Lens, Sabela</creatorcontrib><creatorcontrib>Pallett, Laura J.</creatorcontrib><creatorcontrib>Testoni, Barbara</creatorcontrib><creatorcontrib>Rodríguez-Tajes, Sergio</creatorcontrib><creatorcontrib>Mariño, Zoe</creatorcontrib><creatorcontrib>Bartres, Concepción</creatorcontrib><creatorcontrib>García-Pras, Ester</creatorcontrib><creatorcontrib>Leonel, Thais</creatorcontrib><creatorcontrib>Perpiñán, Elena</creatorcontrib><creatorcontrib>Lozano, Juan José</creatorcontrib><creatorcontrib>Rodríguez-Frías, Francisco</creatorcontrib><creatorcontrib>Koutsoudakis, George</creatorcontrib><creatorcontrib>Zoulim, Fabien</creatorcontrib><creatorcontrib>Maini, Mala K.</creatorcontrib><creatorcontrib>Forns, Xavier</creatorcontrib><creatorcontrib>Pérez-del-Pulgar, Sofía</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García-López, Mireia</au><au>Lens, Sabela</au><au>Pallett, Laura J.</au><au>Testoni, Barbara</au><au>Rodríguez-Tajes, Sergio</au><au>Mariño, Zoe</au><au>Bartres, Concepción</au><au>García-Pras, Ester</au><au>Leonel, Thais</au><au>Perpiñán, Elena</au><au>Lozano, Juan José</au><au>Rodríguez-Frías, Francisco</au><au>Koutsoudakis, George</au><au>Zoulim, Fabien</au><au>Maini, Mala K.</au><au>Forns, Xavier</au><au>Pérez-del-Pulgar, Sofía</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Viral and immune factors associated with successful treatment withdrawal in HBeAg-negative chronic hepatitis B patients</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2021-05</date><risdate>2021</risdate><volume>74</volume><issue>5</issue><spage>1064</spage><epage>1074</epage><pages>1064-1074</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><abstract>Factors associated with a successful outcome upon nucleos(t)ide analogue (NA) treatment withdrawal in HBeAg-negative chronic hepatitis B (CHB) patients have yet to be clarified. The objective of this study was to analyse the HBV-specific T cell response, in parallel with peripheral and intrahepatic viral parameters, in patients undergoing NA discontinuation. Twenty-seven patients without cirrhosis with HBeAg-negative CHB with complete viral suppression (&gt;3 years) were studied prospectively. Intrahepatic HBV-DNA (iHBV-DNA), intrahepatic HBV-RNA (iHBV-RNA), and covalently closed circular DNA (cccDNA) were quantified at baseline. Additionally, serum markers (HBV-DNA, HBsAg, HBV core-related antigen [HBcrAg] and HBV-RNA) and HBV-specific T cell responses were analysed at baseline and longitudinally throughout follow-up. After a median follow-up of 34 months, 22/27 patients (82%) remained off-therapy, of whom 8 patients (30% of the total cohort) lost HBsAg. Baseline HBsAg significantly correlated with iHBV-DNA and iHBV-RNA, and these parameters were lower in patients who lost HBsAg. All patients had similar levels of detectable cccDNA regardless of their clinical outcome. Patients achieving functional cure had baseline HBsAg levels ≤1,000 IU/ml. Similarly, an increased frequency of functional HBV-specific CD8+ T cells at baseline was associated with sustained viral control off treatment. These HBV-specific T cell responses persisted, but did not increase, after treatment withdrawal. A similar, but not statistically significant trend, was observed for HBV-specific CD4+ T cell responses. Decreased cccDNA transcription and low HBsAg levels are associated with HBsAg loss upon NA discontinuation in patients with HBeAg-negative CHB. The presence of functional HBV-specific T cells at baseline are associated with a successful outcome after treatment withdrawal. Nucleos(t)ide analogue therapy can be discontinued in a high proportion of chronic hepatitis B patients without cirrhosis. The strength of HBV-specific immune T cell responses may contribute to successful viral control after antiviral treatment interruption. Our comprehensive study provides in-depth data on virological and immunological factors than can help guide individualised therapy in patients with chronic hepatitis B. [Display omitted] •Stopping NA is feasible in a high proportion of HBeAg-negative CHB patients.•Low baseline HBsAg titres identify patients who will achieve functional cure.•Reduced cccDNA activity is associated with HBsAg loss after NA discontinuation.•HBV-specific T cell functionality may influence patient outcome upon NA withdrawal.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33278456</pmid><doi>10.1016/j.jhep.2020.11.043</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7613-3908</orcidid><orcidid>https://orcid.org/0000-0003-4900-411X</orcidid><orcidid>https://orcid.org/0000-0002-8188-1764</orcidid><orcidid>https://orcid.org/0000-0001-5588-5465</orcidid><orcidid>https://orcid.org/0000-0002-2245-0083</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0168-8278
ispartof Journal of hepatology, 2021-05, Vol.74 (5), p.1064-1074
issn 0168-8278
1600-0641
language eng
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source Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)
subjects Antiviral Agents - therapeutic use
Antiviral therapy discontinuation
Biomarkers - blood
CD4 antigen
CD8 antigen
Chronic hepatitis B
Circular DNA
Circular RNA
Cirrhosis
Covalently closed circular DNA
DNA, Circular - isolation & purification
DNA, Viral - isolation & purification
Female
HBcrAg
HBsAg
HBV-RNA
HBV-Specific T cells
Hepatitis B
Hepatitis B Antigens - analysis
Hepatitis B Antigens - isolation & purification
Hepatitis B e antigen
Hepatitis B surface antigen
Hepatitis B Surface Antigens - analysis
Hepatitis B virus
Hepatitis B virus - genetics
Hepatitis B virus - isolation & purification
Hepatitis B, Chronic - blood
Hepatitis B, Chronic - diagnosis
Human health and pathology
Humans
Hépatology and Gastroenterology
Immune response
Immunity, Cellular - drug effects
Immunity, Cellular - immunology
Interferon
Life Sciences
Liver - pathology
Liver - virology
Liver cirrhosis
Lymphocytes
Lymphocytes T
Male
Middle Aged
Nucleos(t)ide analogue
Nucleosides - therapeutic use
Patient Care Planning
Patients
Ribonucleic acid
RNA
Statistical analysis
Transcription
Withholding Treatment - statistics & numerical data
title Viral and immune factors associated with successful treatment withdrawal in HBeAg-negative chronic hepatitis B patients
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