Gastrointestinal Foxp3 expression in normal, inflammatory and neoplastic conditions

Pathology. 2011 Aug;43(5):465-71. doi: 10.1097/PAT.0b013e3283485e37.

Abstract

Background: Foxp3(+) regulatory T lymphocytes (T-regs) represent an important regulatory cell subset in inflammatory, preneoplastic and neoplastic conditions of the gastrointestinal tract.

Methods: Inflammatory, preneoplastic and neoplastic conditions of the gastrointestinal tract (189 cases) were studied with the evaluation of Foxp3 regulatory T cells based on immunohistochemistry.

Results: Few Foxp3(+) cells were found in controls and inflammatory conditions (oesophagitis, gastritis, coeliac disease, inflammatory bowel disease); in preneoplastic and neoplastic conditions the number of Foxp3(+) cells was significatively increased.

Conclusions: In normal conditions the number of mucosal lymphocytes is very low throughout the gastro-intestinal tract; in active coeliac disease patients or on a gluten-free diet, only a slight increase in Foxp3(+) cells may be found. Gastrointestinal cancers are associated with higher Foxp3(+) cell proportion, compared with microscopically normal tissue and with precancerous conditions. However, it is uncertain whether the increase in these regulatory cells is a cause or a consequence of tumour progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Celiac Disease / metabolism
  • Celiac Disease / pathology
  • Cell Count
  • Disease Progression
  • Esophagitis / metabolism
  • Esophagitis / pathology
  • Female
  • Forkhead Transcription Factors / metabolism*
  • Gastric Mucosa / metabolism
  • Gastric Mucosa / pathology
  • Gastritis / metabolism
  • Gastritis / pathology
  • Humans
  • Inflammatory Bowel Diseases / metabolism
  • Inflammatory Bowel Diseases / pathology
  • Lymphocytes / pathology
  • Male
  • Middle Aged
  • Precancerous Conditions / metabolism
  • Precancerous Conditions / pathology*
  • Stomach Diseases / metabolism
  • Stomach Diseases / pathology*
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology
  • Young Adult

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors