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Oral Abstracts (Abstracts 1–263)
Author(s) -
Romain Désert,
Christelle Reynès,
Robert Sabatier,
Damien Grégoire,
Florian Rohart,
Anne Corlu,
Frédéric Canal,
Marie Sicard,
Mireille Desille,
Stéphanie Renaud,
Bruno Turlin,
Laurent Sulpice,
Damien Bergeat,
Pascale Bellaud,
Christine Perret,
Bruno Clément,
KimAnh Lê Cao,
Orlando Musso
Publication year - 2017
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.29500
Subject(s) - medicine
[[abstract]]Background and aims: The functional cure, seroclearance of hepatitis B surface antigen (HBsAg), is a desired goal for patients with chronic hepatitis B (CHB), who often show weak or absent virus-specific immunity due to programmed cell death 1 (PD-1)-associated T cell exhaustion . We aim to assess soluble PD-1 (sPD-1) as a novel seromarker for spontaneous HBsAg seroclearance . Method: Baseline and follow-up serum level of sPD-1 was evalu ated in all 1,046 patients from the REVEAL-HBV study who were hepatitis B e antigen-seronegative with serum HBV DNA undetectability until HBsAg seroclearance or the end of follow-up . sPD-1 levels were categorized in four groups (≥4000, 536-3999, 125-535, <125 pg/mL) according to upper and lower limits, and median level of quantification . We used multiple regression analyses to assess associations of baseline sPD-1 level with HBsAg decline during follow-up, and of baseline sPD-1 and its reduction with spontaneous HBsAg seroclearance . Odds ratio (OR) and rate ratio (RR) with 95% confidence interval (95% CI) were used to estimate magnitudes of associations . Results: A total of 390 patients achieved spontaneous HBsAg seroclearance during a mean 5 .4 years of follow-up . Baseline sPD-1 levels were correlated with qHBsAg levels (P<0 .0001), and associated with decline in HBsAg during follow-up (OR (95% CI) for ≥0 .5 log annual decline= 4 .7 (1 .7-12 .8), P=0 .002 for baseline sPD-1 <536 vs . ≥4000 pg/ mL) . Incidence rates of spontaneous HBsAg seroclearance increased with decreasing levels of baseline sPD-1 from 11 .5, 61 .7, 96 .7, to 151 .0 per 1000 person-years for sPD-1 levels ≥4000, 536-3999, 125-535, and <125 pg/mL, respectively (P trend <0 .0001) . After adjustment for gender, age,and alanine aminotransferase level, the RR (95% CI) of HBsAg seroclearance was 5 .7 (3 .8-8 .6), 8 .9 (6 .0-13 .2), and 14 .6 (9 .9-21 .6), respectively, for baseline sPD-1 levels of 536-3999, 125-535, and <125 pg/mL compared to sPD-1 levels of ≥4000 pg/mL . Among patients with baseline sPD-1 levels ≥4000 pg/mL, those who reduced sPD-1 to <125 pg/mL during follow-up had an OR (95% CI) of HBsAg seroclearance of 68 .6 (13 .2-357 .4) compared to those who persistently had sPD-1 >125pg/mL . Four SNPs near the SDC4 gene were associated with baseline sPD-1 levels and subsequent HBsAg seroclearance in a genome-wide association analysis . Conclusion: Reduced sPD-1 levels strongly predict greater chance of HBsAg decline and HBsAg seroclearance in HBeAg-seronegative CHB patients with HBV DNA undetectability . This seromarker may help in patient stratification, and might be considered as a promising target for achieving functional cure for CHB patients