Superantigen immune stimulation evokes epithelial monocyte chemoattractant protein 1 and RANTES production

Infect Immun. 1999 Nov;67(11):6198-202. doi: 10.1128/IAI.67.11.6198-6202.1999.

Abstract

Bacterial superantigens (SAgs) have been implicated in inflammatory disease, and SAg-treated mice have increased jejunal T cells. Here we show that T84 cells (a human epithelial cell line) display increased MCP-1 and RANTES mRNA expression and protein production in response to conditioned medium from Staphylococcus aureus enterotoxin B (SEB; a model SAg)-activated immune cells. Also, MCP-1 and RANTES mRNAs were increased in jejunal enterocytes isolated from SEB-treated mice. We suggest that T-cell recruitment to the gut following SAg immune activation could be partially due to epithelium-derived chemokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Budesonide / pharmacology
  • Chemokine CCL2 / biosynthesis*
  • Chemokine CCL2 / genetics
  • Chemokine CCL5 / biosynthesis*
  • Chemokine CCL5 / genetics
  • Enterotoxins / immunology*
  • Humans
  • Interferon-gamma / pharmacology
  • Monocytes / metabolism*
  • RNA, Messenger / analysis
  • Staphylococcus aureus / immunology*
  • Superantigens / immunology*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Chemokine CCL2
  • Chemokine CCL5
  • Enterotoxins
  • RNA, Messenger
  • Superantigens
  • Tumor Necrosis Factor-alpha
  • enterotoxin B, staphylococcal
  • Budesonide
  • Interferon-gamma