Predictors of sustained functional cure in hepatitis B envelope antigen‐negative patients achieving hepatitis B surface antigen seroclearance with interferon‐alpha–based therapy
Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antig...
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Published in | Journal of viral hepatitis Vol. 26; no. S1; pp. 32 - 41 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.07.2019
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Online Access | Get full text |
ISSN | 1352-0504 1365-2893 1365-2893 |
DOI | 10.1111/jvh.13151 |
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Abstract | Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (HBeAg)‐negative CHB patients. In this prospective study, 176 HBeAg‐negative CHB patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (HBV) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3‐6 months during the 48‐week follow‐up. The sustained functional cure was evaluated. After the 48‐week follow‐up, the sustained functional cure rate was 86.63%. The cumulative rates of HBsAg reversion and HBV DNA reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after HBsAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of HBsAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%, P = 0.022 and 23.81% vs 9.23%, P = 0.014, respectively). Patients with hepatitis B surface antibody (HBsAb) had higher rate of sustained functional cure than patients achieving HBsAg loss but without HBsAb (89.86% vs 73.53%, P = 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [OR] 16.478; 95% confidence interval [CI], 2.135‐127.151; P = 0.007) and high HBsAb levels (OR 8.312; 95% CI, 1.824‐37.881; P = 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after HBsAg clearance and elevated HBsAb levels help to improve functional cure. |
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AbstractList | Hepatitis B surface antigen (
HB
sAg) loss is considered a functional cure in chronic hepatitis B (
CHB
). However, the durability of
HB
sAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (
HB
eAg)‐negative
CHB
patients. In this prospective study, 176
HB
eAg‐negative
CHB
patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (
HBV
) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3‐6 months during the 48‐week follow‐up. The sustained functional cure was evaluated. After the 48‐week follow‐up, the sustained functional cure rate was 86.63%. The cumulative rates of
HB
sAg reversion and
HBV DNA
reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after
HB
sAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of
HB
sAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%,
P
= 0.022 and 23.81% vs 9.23%,
P
= 0.014, respectively). Patients with hepatitis B surface antibody (
HB
sAb) had higher rate of sustained functional cure than patients achieving
HB
sAg loss but without
HB
sAb (89.86% vs 73.53%,
P
= 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [
OR
] 16.478; 95% confidence interval [
CI
], 2.135‐127.151;
P
= 0.007) and high
HB
sAb levels (
OR
8.312; 95%
CI
, 1.824‐37.881;
P
= 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after
HB
sAg clearance and elevated
HB
sAb levels help to improve functional cure. Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (HBeAg)‐negative CHB patients. In this prospective study, 176 HBeAg‐negative CHB patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (HBV) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3‐6 months during the 48‐week follow‐up. The sustained functional cure was evaluated. After the 48‐week follow‐up, the sustained functional cure rate was 86.63%. The cumulative rates of HBsAg reversion and HBV DNA reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after HBsAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of HBsAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%, P = 0.022 and 23.81% vs 9.23%, P = 0.014, respectively). Patients with hepatitis B surface antibody (HBsAb) had higher rate of sustained functional cure than patients achieving HBsAg loss but without HBsAb (89.86% vs 73.53%, P = 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [OR] 16.478; 95% confidence interval [CI], 2.135‐127.151; P = 0.007) and high HBsAb levels (OR 8.312; 95% CI, 1.824‐37.881; P = 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after HBsAg clearance and elevated HBsAb levels help to improve functional cure. Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (HBeAg)‐negative CHB patients. In this prospective study, 176 HBeAg‐negative CHB patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (HBV) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3‐6 months during the 48‐week follow‐up. The sustained functional cure was evaluated. After the 48‐week follow‐up, the sustained functional cure rate was 86.63%. The cumulative rates of HBsAg reversion and HBV DNA reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after HBsAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of HBsAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%, P = 0.022 and 23.81% vs 9.23%, P = 0.014, respectively). Patients with hepatitis B surface antibody (HBsAb) had higher rate of sustained functional cure than patients achieving HBsAg loss but without HBsAb (89.86% vs 73.53%, P = 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [OR] 16.478; 95% confidence interval [CI], 2.135‐127.151; P = 0.007) and high HBsAb levels (OR 8.312; 95% CI, 1.824‐37.881; P = 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after HBsAg clearance and elevated HBsAb levels help to improve functional cure. Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (HBeAg)-negative CHB patients. In this prospective study, 176 HBeAg-negative CHB patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (HBV) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3-6 months during the 48-week follow-up. The sustained functional cure was evaluated. After the 48-week follow-up, the sustained functional cure rate was 86.63%. The cumulative rates of HBsAg reversion and HBV DNA reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after HBsAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of HBsAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%, P = 0.022 and 23.81% vs 9.23%, P = 0.014, respectively). Patients with hepatitis B surface antibody (HBsAb) had higher rate of sustained functional cure than patients achieving HBsAg loss but without HBsAb (89.86% vs 73.53%, P = 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [OR] 16.478; 95% confidence interval [CI], 2.135-127.151; P = 0.007) and high HBsAb levels (OR 8.312; 95% CI, 1.824-37.881; P = 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after HBsAg clearance and elevated HBsAb levels help to improve functional cure.Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping treatment remains unknown. This study aimed to assess the sustained functional cure achieved by interferon therapy in hepatitis B envelope antigen (HBeAg)-negative CHB patients. In this prospective study, 176 HBeAg-negative CHB patients with functional cure were enrolled for 12 weeks of cessation treatment, and treatment information and baseline data were collected. Hepatitis B virus (HBV) biomarkers and clinical biochemical indicators were evaluated every 3 months; liver imaging examinations were performed every 3-6 months during the 48-week follow-up. The sustained functional cure was evaluated. After the 48-week follow-up, the sustained functional cure rate was 86.63%. The cumulative rates of HBsAg reversion and HBV DNA reversion were 12.79% and 2.33%, respectively. Consolidation treatment ≥ 12 weeks after HBsAg loss achieved a significantly higher rate of sustained functional cure and significantly lower rate of HBsAg reversion than consolidation treatment < 12 weeks (76.19% vs 90.00%, P = 0.022 and 23.81% vs 9.23%, P = 0.014, respectively). Patients with hepatitis B surface antibody (HBsAb) had higher rate of sustained functional cure than patients achieving HBsAg loss but without HBsAb (89.86% vs 73.53%, P = 0.012). Consolidation treatment ≥ 12 weeks (odds ratio [OR] 16.478; 95% confidence interval [CI], 2.135-127.151; P = 0.007) and high HBsAb levels (OR 8.312; 95% CI, 1.824-37.881; P = 0.006) were independent predictors of sustained functional cure. Results suggested that 12 weeks of consolidation therapy after HBsAg clearance and elevated HBsAb levels help to improve functional cure. |
Author | Wu, Shu‐Ling Cao, Wei‐Hua Yi, Wei Li, Ming‐Hui Lu, Hui‐Hui Gao, Yuan‐Jiao Chang, Min Hu, Lei‐Ping Wan, Gang Hao, Hong‐Xiao Chen, Qi‐Qi Zhang, Lu Xie, Yao Shen, Ge Lu, Yao Liu, Ru‐Yu Li, Jun‐Nan |
Author_xml | – sequence: 1 givenname: Ming‐Hui surname: Li fullname: Li, Ming‐Hui organization: Capital Medical University – sequence: 2 givenname: Wei surname: Yi fullname: Yi, Wei organization: Capital Medical University – sequence: 3 givenname: Lu surname: Zhang fullname: Zhang, Lu organization: Capital Medical University – sequence: 4 givenname: Yao surname: Lu fullname: Lu, Yao organization: Capital Medical University – sequence: 5 givenname: Hui‐Hui surname: Lu fullname: Lu, Hui‐Hui organization: Capital Medical University – sequence: 6 givenname: Ge surname: Shen fullname: Shen, Ge organization: Capital Medical University – sequence: 7 givenname: Shu‐Ling surname: Wu fullname: Wu, Shu‐Ling organization: Capital Medical University – sequence: 8 givenname: Hong‐Xiao surname: Hao fullname: Hao, Hong‐Xiao organization: Capital Medical University – sequence: 9 givenname: Yuan‐Jiao surname: Gao fullname: Gao, Yuan‐Jiao organization: Capital Medical University – sequence: 10 givenname: Min surname: Chang fullname: Chang, Min organization: Capital Medical University – sequence: 11 givenname: Ru‐Yu surname: Liu fullname: Liu, Ru‐Yu organization: Capital Medical University – sequence: 12 givenname: Lei‐Ping surname: Hu fullname: Hu, Lei‐Ping organization: Capital Medical University – sequence: 13 givenname: Wei‐Hua surname: Cao fullname: Cao, Wei‐Hua organization: Capital Medical University – sequence: 14 givenname: Qi‐Qi surname: Chen fullname: Chen, Qi‐Qi organization: Capital Medical University – sequence: 15 givenname: Jun‐Nan surname: Li fullname: Li, Jun‐Nan organization: Capital Medical University – sequence: 16 givenname: Gang surname: Wan fullname: Wan, Gang organization: Capital Medical University – sequence: 17 givenname: Yao surname: Xie fullname: Xie, Yao email: xieyao00120184@sina.com organization: Capital Medical University |
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Cites_doi | 10.1016/S0140-6736(05)17701-0 10.1002/hep.1840130403 10.1016/S0168-8278(87)80008-9 10.1093/infdis/jir283 10.1111/liv.13006 10.1002/hep.22295 10.1056/NEJMoa043470 10.7326/0003-4819-150-2-200901200-00100 10.1016/j.intimp.2005.06.004 10.1053/j.gastro.2008.05.031 10.1099/vir.0.020552-0 10.1002/hep.28156 10.1111/jvh.12736 10.1046/j.1365-2893.2003.00487.x 10.1016/j.ijid.2016.03.024 10.1016/j.jhep.2014.05.044 10.1007/s12072-014-9571-3 10.1111/jvh.12755 10.1053/j.gastro.2008.07.008 10.1002/hep.21612 10.1002/hep.22945 10.1053/j.gastro.2015.09.043 10.1002/hep.23327 10.1007/s10620-014-3486-7 10.1128/JVI.75.6.2684-2691.2001 10.1126/science.1243462 10.1016/j.cld.2007.08.001 10.1053/j.gastro.2010.04.052 10.1128/JVI.74.9.4165-4173.2000 10.1016/j.jhep.2009.01.016 10.1128/JVI.00933-15 10.1016/j.jhep.2017.03.021 10.1093/infdis/jiv547 10.1172/JCI58847 10.1053/j.gastro.2009.06.054 10.1080/14712598.2018.1518423 10.1007/s12072-015-9675-4 10.1016/j.jhep.2017.09.018 10.1007/s10059-011-1059-6 10.1136/gutjnl-2013-305517 10.1128/JVI.73.1.474-481.1999 10.1016/j.imbio.2014.07.020 10.3851/IMP1497 10.1111/liv.12661 |
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Keywords | chronic hepatitis B hepatitis B e antigen negative functional cure hepatitis B surface antigen loss interferon |
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References | 2015; 35 2010; 15 2012; 122 2014; 219 2005; 352 1991; 13 1987; 4 2017; 24 2017; 67 2016; 10 2011; 32 2009; 150 2014; 63 2015; 9 2014; 61 2007; 11 2016; 36 2009; 49 2009; 137 2018; 68 2011; 204 2015; 89 2004; 11 2018; 18 2015; 60 2009; 50 2005; 365 2010; 139 2017; 11 2000; 74 2005; 5 2008; 48 2016; 63 1999; 73 2016; 213 2013 2008; 135 2010; 91 2007; 45 2010; 51 2016; 46 2014; 343 2001; 75 2016; 150 e_1_2_9_30_1 e_1_2_9_31_1 e_1_2_9_11_1 e_1_2_9_34_1 e_1_2_9_10_1 e_1_2_9_35_1 e_1_2_9_13_1 e_1_2_9_32_1 e_1_2_9_12_1 e_1_2_9_33_1 Papatheodoridis GV (e_1_2_9_9_1) 2017; 11 e_1_2_9_15_1 e_1_2_9_38_1 e_1_2_9_14_1 e_1_2_9_39_1 e_1_2_9_17_1 e_1_2_9_36_1 e_1_2_9_16_1 e_1_2_9_37_1 e_1_2_9_19_1 e_1_2_9_18_1 e_1_2_9_41_1 e_1_2_9_42_1 e_1_2_9_20_1 e_1_2_9_40_1 e_1_2_9_22_1 e_1_2_9_45_1 e_1_2_9_21_1 e_1_2_9_46_1 e_1_2_9_24_1 e_1_2_9_43_1 e_1_2_9_23_1 e_1_2_9_44_1 e_1_2_9_8_1 e_1_2_9_7_1 e_1_2_9_6_1 e_1_2_9_5_1 e_1_2_9_4_1 e_1_2_9_3_1 e_1_2_9_2_1 e_1_2_9_26_1 e_1_2_9_25_1 e_1_2_9_28_1 e_1_2_9_47_1 e_1_2_9_27_1 e_1_2_9_29_1 |
References_xml | – volume: 150 start-page: 134 year: 2016 end-page: 144 article-title: Combination of tenofovir disoproxil fumarate and peginterferon α‐2a increases loss of hepatitis B surface antigen in patients with chronic Hepatitis B publication-title: Gastroenterology – volume: 11 start-page: S4 year: 2017 end-page: S5 article-title: Incidence and risk prediction of hepatocellular carcinoma: a retrospective analysis of the S‐collate study publication-title: Hepatol Int – volume: 68 start-page: 63 year: 2018 end-page: 72 article-title: Durability of hepatitis B surface antigen seroclearance in untreated and nucleos(t)ide analogue‐treated patients publication-title: J Hepatol – volume: 135 start-page: 1192 year: 2008 end-page: 1199 article-title: HBsAg Seroclearance in chronic hepatitis B in Asian patients: replicative level and risk of hepatocellular carcinoma publication-title: Gastroenterology – volume: 13 start-page: 627 year: 1991 end-page: 631 article-title: Incidence, determinants and significance of delayed clearance of serum HBsAg in chronic hepatitis B virus infection: a prospective study publication-title: Hepatology – volume: 365 start-page: 123 year: 2005 end-page: 129 article-title: Pegylated interferon alfa‐2b alone or in combination with lamivudine for HBeAg‐positive chronic hepatitis B: a randomised trial publication-title: Lancet – volume: 4 start-page: 45 year: 1987 end-page: 51 article-title: Clearance of hepatitis B surface antigen (HBsAg) after surgical resection of hepatocellular carcinoma publication-title: J Hepatol – volume: 35 start-page: 130 year: 2015 end-page: 139 article-title: Loss of hepatitis B surface antigen in a real‐life clinical cohort of patients with chronic hepatitis B virus infection publication-title: Liver Int – volume: 204 start-page: 408 year: 2011 end-page: 414 article-title: Viral determinants of hepatitis B surface antigen seroclearance in hepatitis B e antigen‐negative chronic hepatitis B patients publication-title: J Infect Dis – volume: 50 start-page: 1084 year: 2009 end-page: 1092 article-title: High rates of HBsAg seroconversion in HBeAg‐positive chronic hepatitis B patients responding to interferon: a long‐term follow‐up study publication-title: J Hepatol – volume: 49 start-page: S156 year: 2009 end-page: S165 article-title: Reactivation of hepatitis B publication-title: Hepatology – volume: 24 start-page: 12 issue: suppl 1 year: 2017 end-page: 20 article-title: Peginterferon is preferable to entecavir for prevention of unfavourable events in patients with HBeAg‐positive chronic hepatitis B: a five‐year observational cohort study publication-title: J Viral Hepat – volume: 36 start-page: 100 issue: suppl 1 year: 2016 end-page: 104 article-title: The prognosis and management of inactive HBV carriers publication-title: Liver Int – volume: 343 start-page: 1221 year: 2014 end-page: 1228 article-title: Specific and nonhepatotoxic degradation of nuclear hepatitis B virus cccDNA publication-title: Science – volume: 5 start-page: 1839 year: 2005 end-page: 1852 article-title: Impaired function of hepatic natural killer cells from murine chronic HBsAg carriers publication-title: Int Immunopharmacol – volume: 10 start-page: 1 year: 2016 end-page: 98 article-title: Asian‐Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update publication-title: Hepatol Int – volume: 122 start-page: 529 year: 2012 end-page: 537 article-title: IFN‐alpha inhibits HBV transcription and replication in cell culture and in humanized mice by targeting the epigenetic regulation of the nuclear cccDNA minichromosome publication-title: J Clin Invest – volume: 45 start-page: 1187 year: 2007 end-page: 1192 article-title: HBsAg seroclearance in asymptomatic carriers of high endemic areas: appreciably high rates during a long‐term follow‐up publication-title: Hepatology – volume: 67 start-page: 370 year: 2017 end-page: 398 article-title: EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection publication-title: J Hepatol – volume: 139 start-page: 483 year: 2010 end-page: 490 article-title: Hepatitis B surface anti‐gen serum levels help to distinguish active from inactive hepatitis B virus genotype D carriers publication-title: Gastroenterology – volume: 89 start-page: 9200 year: 2015 end-page: 9212 article-title: The Interferon‐ inducible protein tetherin inhibits hepatitis B virus virion secretion publication-title: J Virol – volume: 48 start-page: 88 year: 2008 end-page: 98 article-title: The antiviral drug selected hepatitis B virus rtA181T/sW172/mutant has a dominant negative secretion defect and alters the typical profile of viral rebound publication-title: Hepatology – volume: 137 start-page: 1289 year: 2009 end-page: 1300 article-title: Temporal analysis of early immune responses in patients with acute hepatitis B virus infection publication-title: Gastroenterology – volume: 219 start-page: 944 year: 2014 end-page: 949 article-title: Hepatitis B virus e antigen (HBeAg) may have a negative effect on dendritic cell generation publication-title: Immunobiology – volume: 9 start-page: 9 year: 2015 end-page: 16 article-title: How to achieve immune control in chronic hepatitis B? publication-title: Hepatol Int – volume: 73 start-page: 474 year: 1999 end-page: 481 article-title: Hepatitis B virus RNA‐binding proteins associated with cytokine‐induced clearance of viral RNA from the liver of transgenic mice publication-title: J Virol – volume: 46 start-page: 42 year: 2016 end-page: 48 article-title: Impact of HBeAg on the maturation and function of dendritic cells publication-title: Int J Infect Dis – volume: 11 start-page: 97 year: 2004 end-page: 107 article-title: Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures publication-title: J Viral Hepat – volume: 15 start-page: 133 year: 2010 end-page: 143 article-title: Hepatitis B surface antigen seroclearance during chronic HBV infection publication-title: Antivir Ther – volume: 32 start-page: 167 year: 2011 end-page: 172 article-title: PKR‐dependent mechanisms of interferon‐alpha for inhibiting hepatitis B virus replication publication-title: Mol Cells – volume: 74 start-page: 4165 year: 2000 end-page: 4173 article-title: Intrahepatic induction of alpha/beta interferon eliminates viral RNA‐containing capsids in hepatitis B virus transgenic mice publication-title: J Virol – volume: 150 start-page: 104 year: 2009 end-page: 110 article-title: National Institutes of Health consensus development conference statement: management of hepatitis B publication-title: Ann Intern Med – volume: 213 start-page: 966 year: 2016 end-page: 974 article-title: Peg‐interferon is superior to nucleos(t)ide analogues for prevention of hepatocellular carcinoma in chronic hepatitis B publication-title: J Infect Dis – volume: 24 start-page: 1089 year: 2017 end-page: 1097 article-title: Hepatitis B surface antigen loss and sustained viral suppression in Asian chronic hepatitis B patients: a community‐based real‐world study publication-title: J Viral Hepat – volume: 61 start-page: 777 year: 2014 end-page: 784 article-title: Switching from entecavir to PegIFN alfa‐2a in patients with HBeAg‐positive chronic hepatitis B: a randomised open‐label trial (OSST trial) publication-title: J Hepatol – volume: 63 start-page: 1325 year: 2014 end-page: 1332 article-title: HBsAg seroclearance after nucleoside analogue therapy in patients with chronic hepatitis B: clinical outcomes and durability publication-title: Gut – volume: 352 start-page: 2682 year: 2005 end-page: 2695 article-title: Peginterferon alfa‐2a, lamivudine, and the combination for HBeAg‐positive chronic hepatitis B publication-title: N Engl J Med – volume: 91 start-page: 2080 year: 2010 end-page: 2090 article-title: Hepatitis B virus polymerase inhibits RIG‐I‐ and Toll‐like receptor 3‐mediated beta interferon induction in human hepatocytes through interference with interferon regulatory factor 3 activation and dampening of the interaction between TBK1/IKKepsilon and DDX3 publication-title: J Gen Virol – volume: 63 start-page: 261 year: 2016 end-page: 283 article-title: AASLD guidelines for treatment of chronic hepatitis B publication-title: Hepatology – volume: 18 start-page: 1085 issue: 10 year: 2018 end-page: 1094 article-title: Interferon‐based treatment is superior to nucleos(t)ide analog in reducing HBV‐related hepatocellular carcinoma for chronic hepatitis B patients at high risk publication-title: Expert Opin Biol Ther – volume: 51 start-page: 422 year: 2010 end-page: 430 article-title: Entecavir treatment for up to 5 years in patients with hepatitis B e antigen‐positive chronic hepatitis B publication-title: Hepatology – volume: 75 start-page: 2684 year: 2001 end-page: 2691 article-title: Inhibition of hepatitis B virus replication by the interferon‐inducible MxA protein publication-title: J Virol – volume: 135 start-page: 459 year: 2008 end-page: 467 article-title: Sustained HBeAg and HBsAg loss after long‐term follow‐up of HBeAg‐positive patients treated with peginterferon alpha‐2b publication-title: Gastroenterology – volume: 11 start-page: 727 year: 2007 end-page: 759 article-title: The immunology of hepatitis B publication-title: Clin Liver Dis – volume: 60 start-page: 1457 year: 2015 end-page: 1464 article-title: Seven‐year efficacy and safety of treatment with tenofovir disoproxil fumarate for chronic hepatitis B virus infection publication-title: Dig Dis Sci – year: 2013 – ident: e_1_2_9_20_1 doi: 10.1016/S0140-6736(05)17701-0 – ident: e_1_2_9_17_1 doi: 10.1002/hep.1840130403 – ident: e_1_2_9_16_1 doi: 10.1016/S0168-8278(87)80008-9 – ident: e_1_2_9_18_1 doi: 10.1093/infdis/jir283 – ident: e_1_2_9_34_1 doi: 10.1111/liv.13006 – ident: e_1_2_9_42_1 doi: 10.1002/hep.22295 – ident: e_1_2_9_21_1 doi: 10.1056/NEJMoa043470 – ident: e_1_2_9_44_1 doi: 10.7326/0003-4819-150-2-200901200-00100 – ident: e_1_2_9_28_1 doi: 10.1016/j.intimp.2005.06.004 – ident: e_1_2_9_12_1 doi: 10.1053/j.gastro.2008.05.031 – volume: 11 start-page: S4 year: 2017 ident: e_1_2_9_9_1 article-title: Incidence and risk prediction of hepatocellular carcinoma: a retrospective analysis of the S‐collate study publication-title: Hepatol Int – ident: e_1_2_9_25_1 doi: 10.1099/vir.0.020552-0 – ident: e_1_2_9_3_1 doi: 10.1002/hep.28156 – ident: e_1_2_9_31_1 doi: 10.1111/jvh.12736 – ident: e_1_2_9_45_1 doi: 10.1046/j.1365-2893.2003.00487.x – ident: e_1_2_9_27_1 doi: 10.1016/j.ijid.2016.03.024 – ident: e_1_2_9_8_1 doi: 10.1016/j.jhep.2014.05.044 – ident: e_1_2_9_30_1 doi: 10.1007/s12072-014-9571-3 – ident: e_1_2_9_5_1 doi: 10.1111/jvh.12755 – ident: e_1_2_9_15_1 doi: 10.1053/j.gastro.2008.07.008 – ident: e_1_2_9_14_1 doi: 10.1002/hep.21612 – ident: e_1_2_9_46_1 doi: 10.1002/hep.22945 – ident: e_1_2_9_7_1 doi: 10.1053/j.gastro.2015.09.043 – ident: e_1_2_9_22_1 doi: 10.1002/hep.23327 – ident: e_1_2_9_23_1 doi: 10.1007/s10620-014-3486-7 – ident: e_1_2_9_38_1 doi: 10.1128/JVI.75.6.2684-2691.2001 – ident: e_1_2_9_35_1 doi: 10.1126/science.1243462 – ident: e_1_2_9_47_1 doi: 10.1016/j.cld.2007.08.001 – ident: e_1_2_9_33_1 doi: 10.1053/j.gastro.2010.04.052 – ident: e_1_2_9_37_1 doi: 10.1128/JVI.74.9.4165-4173.2000 – ident: e_1_2_9_13_1 doi: 10.1016/j.jhep.2009.01.016 – ident: e_1_2_9_41_1 doi: 10.1128/JVI.00933-15 – ident: e_1_2_9_2_1 doi: 10.1016/j.jhep.2017.03.021 – ident: e_1_2_9_10_1 doi: 10.1093/infdis/jiv547 – ident: e_1_2_9_36_1 doi: 10.1172/JCI58847 – ident: e_1_2_9_24_1 doi: 10.1053/j.gastro.2009.06.054 – ident: e_1_2_9_6_1 doi: 10.1080/14712598.2018.1518423 – ident: e_1_2_9_4_1 doi: 10.1007/s12072-015-9675-4 – ident: e_1_2_9_32_1 doi: 10.1016/j.jhep.2017.09.018 – ident: e_1_2_9_40_1 doi: 10.1007/s10059-011-1059-6 – ident: e_1_2_9_43_1 doi: 10.1136/gutjnl-2013-305517 – ident: e_1_2_9_11_1 – ident: e_1_2_9_39_1 doi: 10.1128/JVI.73.1.474-481.1999 – ident: e_1_2_9_26_1 doi: 10.1016/j.imbio.2014.07.020 – ident: e_1_2_9_29_1 doi: 10.3851/IMP1497 – ident: e_1_2_9_19_1 doi: 10.1111/liv.12661 |
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Snippet | Hepatitis B surface antigen (HBsAg) loss is considered a functional cure in chronic hepatitis B (CHB). However, the durability of HBsAg loss after stopping... Hepatitis B surface antigen ( HB sAg) loss is considered a functional cure in chronic hepatitis B ( CHB ). However, the durability of HB sAg loss after... |
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SubjectTerms | Antigens chronic hepatitis B functional cure Hepatitis Hepatitis B Hepatitis B e antigen hepatitis B e antigen negative Hepatitis B surface antigen hepatitis B surface antigen loss Interferon Patients |
Title | Predictors of sustained functional cure in hepatitis B envelope antigen‐negative patients achieving hepatitis B surface antigen seroclearance with interferon‐alpha–based therapy |
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