B-Cell Activation Gene Signature in Blood and Liver of Hepatitis B e Antigen-Positive Patients With Immune Active Chronic Hepatitis B

J Infect Dis. 2024 Dec 16;230(6):e1263-e1273. doi: 10.1093/infdis/jiae280.

Abstract

Background: Studies on chronic hepatitis B virus (HBV) infection have shown immune dysfunction involving multiple cell types, including T cells. B cells have been evaluated more recently, but in contrast to T cells, more pronounced activation of circulating B cells has been reported. To gain more insight into the activation status of B cells, we investigated gene profiles of B cells in the blood and liver of patients with chronic HBV.

Methods: RNA-sequencing and flow cytometric analysis was performed on peripheral blood B cells of patients with immune active chronic HBV, comparing them with samples from healthy controls. In addition, gene expression profiles of B cells in the liver were analyzed by bulk and single-cell RNA-seq.

Results: Our data show a distinctive B-cell activation gene signature in the blood of patients with immune active chronic HBV, characterized by a significant upregulation of immune-related genes. This peripheral activation profile was also observed in B cells from the liver by single-cell RNA-seq, with naive and memory B-cell subsets being the primary carriers of the signature.

Conclusions: Our findings suggest that B-cell gene profiles reflect responsiveness to HBV infection; these findings are relevant for clinical studies evaluating immunomodulatory treatment strategies for HBV.

Keywords: B cells; activation gene signature; chronic hepatitis B; liver fine-needle aspirates; single-cell RNA sequencing.

MeSH terms

  • Adult
  • B-Lymphocytes* / immunology
  • Female
  • Gene Expression Profiling
  • Hepatitis B e Antigens* / blood
  • Hepatitis B e Antigens* / immunology
  • Hepatitis B virus* / genetics
  • Hepatitis B virus* / immunology
  • Hepatitis B, Chronic* / genetics
  • Hepatitis B, Chronic* / immunology
  • Hepatitis B, Chronic* / virology
  • Humans
  • Liver* / immunology
  • Liver* / virology
  • Lymphocyte Activation* / immunology
  • Male
  • Middle Aged
  • Transcriptome

Substances

  • Hepatitis B e Antigens