Lipopolysaccharide contamination of beta-lactoglobulin affects the immune response against intraperitoneally and orally administered antigen

Int Arch Allergy Immunol. 2004 Nov;135(3):216-20. doi: 10.1159/000081306. Epub 2004 Oct 6.

Abstract

Background: Microbial components in the environment are potent activators of the immune system with capacity to shift the active immune response towards priming of Th1 and/or Th2 cells. Lipopolysaccharide (LPS), a cell-wall component of Gram-negative bacteria, is extensively present in food products like cow's milk. It is not well established, however, how this presence of LPS affects oral tolerance induction.

Methods: We studied the effect of LPS contamination in a commercial preparation of the cow milk protein beta-lactoglobulin (beta-LG) on antigen-specific immune responses. IgG1/IgG2a production upon intraperitoneal immunization without adjuvant was measured, and oral tolerance induction against beta-LG after administration of either an aqueous solution or water-in-oil (w/o) emulsion of beta-LG was evaluated.

Results: LPS contamination of beta-LG provoked a beta-LG-specific IgG2a response, as well as an enhanced beta-LG-specific IgG1 response upon intraperitoneal immunization. Oral tolerance induction to beta-LG was induced by aqueous solutions of beta-LG with and without LPS administration. Conversely, oral administration of w/o-emulsified beta-LG prevented oral tolerance to beta-LG only when the beta-LG was contaminated with LPS.

Conclusions: LPS contamination of an aqueous protein solution does not affect oral tolerance induction, whereas LPS present in emulsion prevents oral tolerance induction towards the food protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Enzyme-Linked Immunosorbent Assay
  • Food Hypersensitivity / immunology*
  • Immune Tolerance / immunology*
  • Immunization
  • Immunoglobulin G / blood
  • Immunoglobulin G / immunology*
  • Injections, Intraperitoneal
  • Lactoglobulins / immunology*
  • Lactoglobulins / pharmacology
  • Lipopolysaccharides / immunology*
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Inbred BALB C

Substances

  • Immunoglobulin G
  • Lactoglobulins
  • Lipopolysaccharides