Intrahepatic IP-10 mRNA and plasma IP-10 levels as response marker for HBeAg-positive chronic hepatitis B patients treated with peginterferon and adefovir

Antiviral Res. 2016 Jul:131:148-55. doi: 10.1016/j.antiviral.2016.05.002. Epub 2016 May 4.

Abstract

Introduction: Interferon-y-inducible protein-10 (IP-10), also called CXCL10, is produced by different types of cells such as monocytes, neutrophils and hepatocytes. IP-10 functions as an inflammatory cytokine, which after binding to its receptor CXCR3, expressed on T-lymphocytes, leads to immune activation. We aimed to establish if IP-10 expression in liver tissue and in plasma of chronic hepatitis B (CHB) patients correlated with each other and further to investigate if IP-10 levels before and during therapy with peginterferon and adefovir could predict treatment outcome in CHB patients.

Patients and methods: A total of 86 CHB patients (41 HBeAg-positive and 45 HBeAg-negative) received combination therapy of peginterferon and adefovir for 48 weeks. Combined Response (CR) (HBeAg-negativity, HBV-DNA ≤ 2000 IU/mL, ALT normalization) and non-response (NR) were assessed at Week 72. Plasma IP-10 levels were measured at baseline and during treatment at Day 3 (D3) and Week 1 (W1). Pre-treatment liver biopsies from 40 of 86 patients were obtained and stored in liquid nitrogen for the analysis of intrahepatic IP-10 mRNA expression.

Results: CR was achieved in 14/41 HBeAg-positive and 17/45 HBeAg-negative patients. Mean baseline plasma IP-10 levels were significantly higher in HBeAg-positive patients with CR than NR (3.20 vs 3.00 log pg/mL p = 0.03); but not in HBeAg-negative patients. Baseline IP-10 levels correlated with ALT-levels in HBeAg-positive and -negative patients (both p < 0.001), and with a decline of HBsAg-levels of ≥0.5 log IU/mL at Week 12 in HBeAg-positive patients (p = 0.001). Plasma IP-10 levels were associated with intrahepatic IP-10 mRNA expression, however, more strongly in HBeAg-positive (R = 0.79, p < 0.001) than in HBeAg-negative patients (R = 0.53, p = 0.011). IP-10 levels only correlated with HAI-scores in HBeAg-positive patients (R = 0.40 p = 0.025). Mean plasma IP-10 levels of both HBeAg-positive and -negative patients increased significantly at D3 compared to baseline (+0.30 log pg/mL p = 0.003), to then decline subsequently at W1 to a level still significantly higher than baseline (+0.14 log pg/mL p < 0.001). The increase of IP-10 was significantly higher in HBeAg-positive patients with NR than in those with CR (+0.35 versus +0.11 log pg/mL p = 0.003).

Conclusions: Baseline plasma IP-10 levels and IP-10 mRNA expression in the liver are correlated with each other, suggesting that plasma IP-10 reflects intrahepatic immune activation. Higher IP-10 levels at baseline seem to be associated with CR in HBeAg-positive patients treated with peginterferon and adefovir, but not in HBeAg-negative patients.

Keywords: Adefovir; Combination therapy; HBV; Interferon-gamma-inducible protein-10 (IP-10); Intrahepatic IP-10 mRNA expression; Peginterferon.

MeSH terms

  • Adenine / analogs & derivatives*
  • Adenine / therapeutic use
  • Adult
  • Alanine Transaminase / blood
  • Antiviral Agents / therapeutic use*
  • Biomarkers / analysis
  • Biomarkers / blood
  • Biopsy
  • Chemokine CXCL10 / blood*
  • Chemokine CXCL10 / genetics*
  • DNA, Viral / blood
  • Drug Therapy, Combination
  • Female
  • Hepatitis B e Antigens / blood
  • Hepatitis B, Chronic / drug therapy
  • Hepatitis B, Chronic / immunology
  • Humans
  • Interferon-alpha / therapeutic use*
  • Liver / immunology*
  • Liver / pathology
  • Male
  • Middle Aged
  • Organophosphonates / therapeutic use*
  • Polyethylene Glycols / therapeutic use*
  • Prospective Studies
  • RNA, Messenger
  • Recombinant Proteins / therapeutic use
  • Treatment Outcome

Substances

  • Antiviral Agents
  • Biomarkers
  • CXCL10 protein, human
  • Chemokine CXCL10
  • DNA, Viral
  • Hepatitis B e Antigens
  • Interferon-alpha
  • Organophosphonates
  • RNA, Messenger
  • Recombinant Proteins
  • Polyethylene Glycols
  • adefovir
  • Alanine Transaminase
  • Adenine
  • peginterferon alfa-2a