APRIL-producing eosinophils are involved in gastric MALT lymphomagenesis induced by Helicobacter sp infection

Sci Rep. 2020 Sep 9;10(1):14858. doi: 10.1038/s41598-020-71792-3.

Abstract

The roles of the inflammatory response and production of a proliferation-inducing ligand (APRIL) cytokine in gastric mucosa-associated lymphoid tissue (MALT) lymphomagenesis induced by Helicobacter species infection are not clearly understood. We characterized the gastric mucosal inflammatory response associated with gastric MALT lymphoma (GML) and identified APRIL-producing cells in two model systems: an APRIL transgenic mouse model of GML induced by Helicobacter infection (Tg-hAPRIL) and human gastric biopsy samples from Helicobacter pylori-infected GML patients. In the mouse model, polarization of T helper 1 (tbet), T helper 2 (gata3), and regulatory T cell (foxp3) responses was evaluated by quantitative PCR. In humans, a significant increase in april gene expression was observed in GML compared to gastritis. APRIL-producing cells were eosinophilic polynuclear cells located within lymphoid infiltrates, and tumoral B lymphocytes were targeted by APRIL. Together, the results of this study demonstrate that the Treg-balanced inflammatory environment is important for gastric lymphomagenesis induced by Helicobacter species, and suggest the pro-tumorigenic potential of APRIL-producing eosinophils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • B-Lymphocytes / immunology*
  • Eosinophils / immunology*
  • Female
  • Gastric Mucosa / immunology
  • Gastric Mucosa / pathology
  • Helicobacter Infections* / complications
  • Helicobacter Infections* / immunology
  • Helicobacter Infections* / pathology
  • Humans
  • Lymphoma, B-Cell, Marginal Zone* / etiology
  • Lymphoma, B-Cell, Marginal Zone* / immunology
  • Lymphoma, B-Cell, Marginal Zone* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Middle Aged
  • T-Lymphocytes / immunology*
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / immunology*

Substances

  • TNFSF13 protein, human
  • Tnfsf13 protein, mouse
  • Tumor Necrosis Factor Ligand Superfamily Member 13