Association of hepatitis B core antibody level and hepatitis B surface antigen clearance in HBeAg-negative patients with chronic hepatitis B

Virulence. 2024 Dec;15(1):2404965. doi: 10.1080/21505594.2024.2404965. Epub 2024 Sep 24.

Abstract

Predicting hepatitis B surface antigen (HBsAg) clearance is important for chronic hepatitis B (CHB) patients receiving pegylated interferon-alfa (Peg-IFN) therapy. We aimed to determine the predictive value of serum hepatitis B core antibody (anti-HBc) for HBsAg clearance. A total of 189 HBeAg-negative CHB patients who received Peg-IFN based therapy were retrospectively included and classified into two groups: nucleos(t)ide analogues (NAs) add-on Peg-IFN group (add-on group, n = 94) and Peg-IFN combined with NAs or Peg-IFN monotherapy group (combination or monotherapy group, n = 95). After 48 weeks of treatment, 27.5% (52/189) and 15.9% (30/189) of patients achieved HBsAg clearance and seroconversion, respectively. Patients in the combination or monotherapy group tended to achieve relatively higher HBsAg clearance (31.6% vs. 23.4%, p = 0.208) and seroconversion (21.1% vs. 10.6%, p = 0.050) rates than those in the add-on group. In combination or monotherapy group, anti-HBc levels at week 12 were lower in patients with HBsAg clearance (9.0 S/CO vs. 9.9 S/CO, p < 0.001) and seroconversion (8.8 S/CO vs. 9.8 S/CO, p < 0.001) than those without. Anti-HBc level at week 12 was an independent predictor of HBsAg clearance and seroconversion. Patients with lower anti-HBc levels at week 12 showed a more significant decline in HBsAg levels during treatment. Combination of anti-HBc at week 12 and baseline HBsAg could identify over 70% of patients who achieved HBsAg clearance after 48 weeks of treatment. In addition to HBsAg, anti-HBc level could be used as a promising marker for selecting HBeAg-negative CHB patients who are more likely to respond to Peg-IFN-based therapy.

Keywords: Hepatitis B surface antigen; antiviral; functional cure; level of anti-HBc antibody; pegylated interferon.

MeSH terms

  • Adult
  • Antiviral Agents* / therapeutic use
  • Drug Therapy, Combination
  • Female
  • Hepatitis B Antibodies* / blood
  • Hepatitis B Core Antigens / blood
  • Hepatitis B Core Antigens / immunology
  • Hepatitis B Surface Antigens* / blood
  • Hepatitis B Surface Antigens* / immunology
  • Hepatitis B e Antigens* / blood
  • Hepatitis B virus / immunology
  • Hepatitis B, Chronic* / blood
  • Hepatitis B, Chronic* / drug therapy
  • Hepatitis B, Chronic* / immunology
  • Hepatitis B, Chronic* / virology
  • Humans
  • Interferon-alpha* / therapeutic use
  • Male
  • Middle Aged
  • Polyethylene Glycols / therapeutic use
  • Recombinant Proteins / immunology
  • Recombinant Proteins / therapeutic use
  • Retrospective Studies
  • Seroconversion
  • Treatment Outcome
  • Young Adult

Substances

  • Hepatitis B Surface Antigens
  • Hepatitis B Antibodies
  • Antiviral Agents
  • Hepatitis B e Antigens
  • Interferon-alpha
  • Hepatitis B Core Antigens
  • Polyethylene Glycols
  • Recombinant Proteins

Grants and funding

Dr Rui Huang wishes to acknowledge the support from Nanjing Medical Science and Technique Development Foundation [JQX21002 and QRX17121], Natural Science Foundation of Jiangsu Province [BK20211004] and the Clinical Trials from the Affiliated Drum Tower Hospital, Medical School of Nanjing University [2022-LCYJ-MS-07]. Dr Jian Wang wishes to acknowledge the support from the National Natural Science Fund [82300719], Clinical Trials from the Affiliated Drum Tower Hospital, Medical School of Nanjing University [2021-LCYJ-PY-43], and Nanjing Medical Science and Technique Development Foundation [YKK21067]. Dr Li Zhu wishes to acknowledge the support from the Clinical Disease Diagnosis and Treatment Technology Foundation of Suzhou [LCZX202117].