Polymorphism in toll-like receptors and helicobacter pylori motility in autoimmune atrophic gastritis and gastric cancer

Valli De Re, Ombretta Repetto, Mariangela De Zorzi, Mariateresa Casarotto, Massimo Tedeschi, Paolo Giuffrida, Marco Vincenzo Lenti, Raffaella Magris, Gianmaria Miolo, Cinzia Mazzon, Giorgio Zanette, Lara Alessandrini, Vincenzo Canzonieri, Laura Caggiari, Stefania Zanussi, Agostino Steffan, Antonio Di Sabatino, Renato Cannizzaro

Research output: Contribution to journalArticle

Abstract

Autoimmune atrophic gastritis (AAG) is associated with an increased risk of certain types of gastric cancer (GC). Helicobacter pylori (H. pylori) infection may have a role in the induction and/or maintenance of AAG and GC. Toll-like receptors (TLR) are essential for H. pylori recognition and subsequent innate and adaptive immunity responses. This study therefore aimed to characterize TLR polymorphisms, and features of bacterial flagellin A in samples from patients with AAG (n = 67), GC (n = 114) and healthy donors (HD; n = 97). TLR5 rs5744174 C/C genotype was associated with GC, lower IgG anti H. pylori response and a higher H. pylori flagellin A abundance and motility. In a subset of patients with AAG, H. pylori strains showed a reduction of the flagellin A abundance and a moderate motility compared with strains from GC patients, a prerequisite for active colonization of the deeper layers of the mucosa, host immune response and inflammation. TLR9 rs5743836 T allele showed an association with serum gastrin G17. In conclusion, our study suggests that alterations of flaA protein, moderate motility in H. pylori and two polymorphisms in TLR5 and TLR9 may favor the onset of AAG and GC, at least in a subset of patients. These findings corroborate the function of pathogen-host cell interactions and responses, likely influencing the pathogenetic process.

Original languageEnglish
Article number648
JournalCancers
Volume11
Issue number5
DOIs
Publication statusPublished - May 1 2019

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Atrophic Gastritis
Toll-Like Receptors
Helicobacter pylori
Stomach Neoplasms
Flagellin
Molecular Motor Proteins
Host-Pathogen Interactions
Gastrins
Helicobacter Infections
Adaptive Immunity
Innate Immunity
Cell Communication
Mucous Membrane
Alleles
Genotype
Maintenance
Tissue Donors
Inflammation
Serum

Keywords

  • Autoimmune gastritis
  • Flagellin A
  • Helicobacter pylori
  • Toll-like receptor 5 (TLR5)
  • Toll-like receptor 9 (TLR9)

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Polymorphism in toll-like receptors and helicobacter pylori motility in autoimmune atrophic gastritis and gastric cancer. / De Re, Valli; Repetto, Ombretta; De Zorzi, Mariangela; Casarotto, Mariateresa; Tedeschi, Massimo; Giuffrida, Paolo; Lenti, Marco Vincenzo; Magris, Raffaella; Miolo, Gianmaria; Mazzon, Cinzia; Zanette, Giorgio; Alessandrini, Lara; Canzonieri, Vincenzo; Caggiari, Laura; Zanussi, Stefania; Steffan, Agostino; Di Sabatino, Antonio; Cannizzaro, Renato.

In: Cancers, Vol. 11, No. 5, 648, 01.05.2019.

Research output: Contribution to journalArticle

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abstract = "Autoimmune atrophic gastritis (AAG) is associated with an increased risk of certain types of gastric cancer (GC). Helicobacter pylori (H. pylori) infection may have a role in the induction and/or maintenance of AAG and GC. Toll-like receptors (TLR) are essential for H. pylori recognition and subsequent innate and adaptive immunity responses. This study therefore aimed to characterize TLR polymorphisms, and features of bacterial flagellin A in samples from patients with AAG (n = 67), GC (n = 114) and healthy donors (HD; n = 97). TLR5 rs5744174 C/C genotype was associated with GC, lower IgG anti H. pylori response and a higher H. pylori flagellin A abundance and motility. In a subset of patients with AAG, H. pylori strains showed a reduction of the flagellin A abundance and a moderate motility compared with strains from GC patients, a prerequisite for active colonization of the deeper layers of the mucosa, host immune response and inflammation. TLR9 rs5743836 T allele showed an association with serum gastrin G17. In conclusion, our study suggests that alterations of flaA protein, moderate motility in H. pylori and two polymorphisms in TLR5 and TLR9 may favor the onset of AAG and GC, at least in a subset of patients. These findings corroborate the function of pathogen-host cell interactions and responses, likely influencing the pathogenetic process.",
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AU - De Re, Valli

AU - Repetto, Ombretta

AU - De Zorzi, Mariangela

AU - Casarotto, Mariateresa

AU - Tedeschi, Massimo

AU - Giuffrida, Paolo

AU - Lenti, Marco Vincenzo

AU - Magris, Raffaella

AU - Miolo, Gianmaria

AU - Mazzon, Cinzia

AU - Zanette, Giorgio

AU - Alessandrini, Lara

AU - Canzonieri, Vincenzo

AU - Caggiari, Laura

AU - Zanussi, Stefania

AU - Steffan, Agostino

AU - Di Sabatino, Antonio

AU - Cannizzaro, Renato

PY - 2019/5/1

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N2 - Autoimmune atrophic gastritis (AAG) is associated with an increased risk of certain types of gastric cancer (GC). Helicobacter pylori (H. pylori) infection may have a role in the induction and/or maintenance of AAG and GC. Toll-like receptors (TLR) are essential for H. pylori recognition and subsequent innate and adaptive immunity responses. This study therefore aimed to characterize TLR polymorphisms, and features of bacterial flagellin A in samples from patients with AAG (n = 67), GC (n = 114) and healthy donors (HD; n = 97). TLR5 rs5744174 C/C genotype was associated with GC, lower IgG anti H. pylori response and a higher H. pylori flagellin A abundance and motility. In a subset of patients with AAG, H. pylori strains showed a reduction of the flagellin A abundance and a moderate motility compared with strains from GC patients, a prerequisite for active colonization of the deeper layers of the mucosa, host immune response and inflammation. TLR9 rs5743836 T allele showed an association with serum gastrin G17. In conclusion, our study suggests that alterations of flaA protein, moderate motility in H. pylori and two polymorphisms in TLR5 and TLR9 may favor the onset of AAG and GC, at least in a subset of patients. These findings corroborate the function of pathogen-host cell interactions and responses, likely influencing the pathogenetic process.

AB - Autoimmune atrophic gastritis (AAG) is associated with an increased risk of certain types of gastric cancer (GC). Helicobacter pylori (H. pylori) infection may have a role in the induction and/or maintenance of AAG and GC. Toll-like receptors (TLR) are essential for H. pylori recognition and subsequent innate and adaptive immunity responses. This study therefore aimed to characterize TLR polymorphisms, and features of bacterial flagellin A in samples from patients with AAG (n = 67), GC (n = 114) and healthy donors (HD; n = 97). TLR5 rs5744174 C/C genotype was associated with GC, lower IgG anti H. pylori response and a higher H. pylori flagellin A abundance and motility. In a subset of patients with AAG, H. pylori strains showed a reduction of the flagellin A abundance and a moderate motility compared with strains from GC patients, a prerequisite for active colonization of the deeper layers of the mucosa, host immune response and inflammation. TLR9 rs5743836 T allele showed an association with serum gastrin G17. In conclusion, our study suggests that alterations of flaA protein, moderate motility in H. pylori and two polymorphisms in TLR5 and TLR9 may favor the onset of AAG and GC, at least in a subset of patients. These findings corroborate the function of pathogen-host cell interactions and responses, likely influencing the pathogenetic process.

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KW - Toll-like receptor 9 (TLR9)

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