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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 |
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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 |
format | article |
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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 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 & 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</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. Published by Elsevier B.V. 2020 European Association for the Study of the Liver</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-f936dd249cb93107cc70e55a270f36771fb52c1a3d4811c2da0b88b2b0557a523</citedby><cites>FETCH-LOGICAL-c517t-f936dd249cb93107cc70e55a270f36771fb52c1a3d4811c2da0b88b2b0557a523</cites><orcidid>0000-0001-7613-3908 ; 0000-0003-4900-411X ; 0000-0002-8188-1764 ; 0000-0001-5588-5465 ; 0000-0002-2245-0083</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33278456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04012145$$DView record in HAL$$Hfree_for_read</backlink></links><search><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><title>Viral and immune factors associated with successful treatment withdrawal in HBeAg-negative chronic hepatitis B patients</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><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 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 & purification</subject><subject>DNA, Viral - isolation & 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 & purification</subject><subject>Hepatitis B e antigen</subject><subject>Hepatitis B surface antigen</subject><subject>Hepatitis B Surface Antigens - analysis</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - isolation & purification</subject><subject>Hepatitis B, Chronic - blood</subject><subject>Hepatitis B, Chronic - diagnosis</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Hépatology and Gastroenterology</subject><subject>Immune response</subject><subject>Immunity, Cellular - drug effects</subject><subject>Immunity, Cellular - immunology</subject><subject>Interferon</subject><subject>Life Sciences</subject><subject>Liver - pathology</subject><subject>Liver - virology</subject><subject>Liver cirrhosis</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nucleos(t)ide analogue</subject><subject>Nucleosides - 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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 (>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.
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•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> |
fulltext | fulltext |
identifier | ISSN: 0168-8278 |
ispartof | Journal of hepatology, 2021-05, Vol.74 (5), p.1064-1074 |
issn | 0168-8278 1600-0641 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8062913 |
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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