Contribution of immunomodulators to gastroesophageal reflux disease and its complications: stromal cells, interleukin 4, and adiponectin

Ann N Y Acad Sci. 2016 Sep;1380(1):183-194. doi: 10.1111/nyas.13157. Epub 2016 Jul 21.

Abstract

Gastroesophageal reflux disease (GERD) has become the most commonly seen gastrointestinal disorder in outpatient clinics. In the United States, around 20% of the general population experience heartburn on a weekly basis. Although clinical complaints can be mild or moderate, patients with GERD may develop further complications, such as peptic strictures, Barrett's esophagus (BE), and even esophageal adenocarcinoma. Pathologically, GERD is developed as a result of chronic and enhanced exposure of the esophageal epithelium to noxious gastric refluxate. In this review article, we provide an overview of GERD and then focus on the roles of stromal cells, interleukin 4, and adiponectin in GERD and BE. The importance of inflammation and immunomodulators in GERD pathogenesis is highlighted. Targeting the immunomodulators or inflammation in general may improve the therapeutic outcome of GERD, in particular, in those refractory to proton pump inhibitors.

Keywords: Barrett's esophagus; adiponectin; gastroesophageal reflux disease; interleukin 4; stromal cells.

Publication types

  • Review

MeSH terms

  • Adiponectin / antagonists & inhibitors
  • Adiponectin / metabolism*
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Gastroesophageal Reflux / complications*
  • Gastroesophageal Reflux / diagnosis
  • Gastroesophageal Reflux / immunology*
  • Humans
  • Immunologic Factors / antagonists & inhibitors
  • Immunologic Factors / metabolism*
  • Interleukin-4 / antagonists & inhibitors
  • Interleukin-4 / metabolism*
  • Stromal Cells / drug effects
  • Stromal Cells / metabolism
  • TRPV Cation Channels / antagonists & inhibitors
  • TRPV Cation Channels / metabolism

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • Anti-Inflammatory Agents
  • IL4 protein, human
  • Immunologic Factors
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Interleukin-4