Plasma CXCL13 is a predictive factor for HBsAg loss and clinical relapse after discontinuation of nucleos(t)ide analogue treatment

Clin Immunol. 2019 Jan:198:31-38. doi: 10.1016/j.clim.2018.11.016. Epub 2018 Nov 30.

Abstract

In this study, we investigated whether plasma cytokine/chemokine levels could predict HBsAg loss or clinical relapse (CR) after stopping nucleos(t)ides analogue (NA) treatment. Theplasma cytokines/chemokines levels were measured at 0, 4, 8, 12, 24 and 48 weeks after NA discontinuation by using the enzyme-linked immunoassay (ELISA) kit. Cox regression analysis revealed that CXCL13 level at the end of treatment (EOT) was an independent predictor for CR (HR 0.26, p < 0.001) and HBsAg loss (HR 3.01, p = 0.008) after treatment cessation. Among the patients with EOT CXCL13 level < 80 pg/ml, the cumulative incidences of CR and HBsAg loss were 65% and 0% at 4 years, respectively. As for the patients with EOT CXCL13 level ≥ 1000 pg/ml, 47.5% cases had HBsAg loss. Our study showed that EOT CXCL13 level was associated with off-treatment response, which may be used to guide cessation of NA treatment in clinical practice.

Keywords: CXCL13; Clinical relapse; Discontinuation; HBsAg loss; Nucleos(t)ide analogue.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Chemokine CXCL13 / blood*
  • Cytokines / blood
  • Female
  • Hepatitis B Surface Antigens / blood*
  • Hepatitis B, Chronic / drug therapy*
  • Hepatitis B, Chronic / immunology
  • Humans
  • Male
  • Middle Aged
  • Nucleosides / therapeutic use
  • Prospective Studies
  • Recurrence

Substances

  • Antiviral Agents
  • CXCL13 protein, human
  • Chemokine CXCL13
  • Cytokines
  • Hepatitis B Surface Antigens
  • Nucleosides