APRIL-producing eosinophils are involved in gastric MALT lymphomagenesis induced by Helicobacter sp infection.
Fiche publication
Date publication
septembre 2020
Journal
Scientific reports
Auteurs
Membres identifiés du Cancéropôle Est :
Dr MARTEYN Benoît
Tous les auteurs :
Blosse A, Peru S, Levy M, Marteyn B, Floch P, Sifré E, Giese A, Prochazkova-Carlotti M, Azzi Martin L, Dubus P, Mégraud F, Ruskone Fournestraux A, Fabiani B, Copie Bergman C, Robe C, Hahne M, Huard B, Lehours P
Lien Pubmed
Résumé
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.
Mots clés
Adult, Animals, B-Lymphocytes, immunology, Eosinophils, immunology, Female, Gastric Mucosa, immunology, Helicobacter Infections, complications, Humans, Lymphoma, B-Cell, Marginal Zone, etiology, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Middle Aged, T-Lymphocytes, immunology, Tumor Necrosis Factor Ligand Superfamily Member 13, immunology
Référence
Sci Rep. 2020 09 9;10(1):14858