Downregulation of B regulatory cells and upregulation of T helper 1 cells in children with Gaucher disease undergoing enzyme replacement therapy

Immunol Res. 2020 Apr;68(2):73-80. doi: 10.1007/s12026-020-09129-5.

Abstract

Gaucher disease (GD) involves a broad spectrum of immunological cells, including T helper (Th) cells and regulatory B cells (Bregs), which function to resolve the immune response and inhibit excessive inflammation. This study aimed to explore T helper cells, B cells, and Bregs in GD children undergoing enzyme replacement therapy (ERT). Our study included 20 GD patients; six patients were categorized as type 1 and 14 as type 3 GD. All patients were on regular ERT. Twenty healthy children were enrolled as controls. All patients and controls were subjected to complete blood analysis, abdominal ultrasound, and flow cytometric detection of T helper cells, B cells, and Bregs. Despite undergoing ERT, CD4+ T helper lymphocytes and Bregs were still significantly lower in patients with GD compared with the controls. Th1 and B cells were more in the patients than in the healthy controls. Lower levels of Bregs were found in type 3, compared with type 1 patients. Increased platelet count was directly associated with increased levels of Bregs and lower levels of B cells. Elevated children's height was also accompanied by decreasing levels of Th1. Our results propose that ERT in GD is associated with partial improvement in immune status, and long-term ERT might be needed for the restoration of the desired immune response levels. Levels of Bregs and Th1 can be employed for monitoring improvement of immune status in GD patients undergoing ERT.

Keywords: B regulatory cells; ERT; Gaucher disease; T helper cells; Th1.

MeSH terms

  • Adolescent
  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocytes, Regulatory / immunology*
  • Child
  • Disease Progression
  • Egypt
  • Enzyme Replacement Therapy / methods*
  • Female
  • Flow Cytometry
  • Gaucher Disease / diagnosis
  • Gaucher Disease / immunology*
  • Humans
  • Immunophenotyping
  • Male
  • Monitoring, Immunologic
  • Phenotype
  • T-Lymphocytes, Helper-Inducer / immunology*
  • Th1 Cells / immunology*