Human Milk Oligosaccharide 3'-GL Improves Influenza-Specific Vaccination Responsiveness and Immunity after Deoxynivalenol Exposure in Preclinical Models

Nutrients. 2021 Sep 14;13(9):3190. doi: 10.3390/nu13093190.

Abstract

Deoxynivalenol (DON), a highly prevalent mycotoxin food contaminant, is known to have immunotoxic effects. In the current study, the potential of dietary interventions with specific mixtures of trans-galactosyl-oligosaccharides (TOS) to alleviate these effects were assessed in a murine influenza vaccination model. Vaccine-specific immune responses were measured in C57Bl/6JOlaHsd mice fed diets containing DON, TOS or a combination, starting 2 weeks before the first vaccination. The direct effects of TOS and its main oligosaccharide, 3'-galactosyl-lactose (3'-GL), on DON-induced damage were studied in Caco-2 cells, as an in vitro model of the intestinal epithelial barrier. Exposure to DON significantly reduced vaccine-specific immune responses and the percentages of Tbet+ Th1 cells and B cells in the spleen. DON significantly altered epithelial structure and integrity in the ileum and reduced the SCFA levels in the cecum. Adding TOS into DON-containing diets significantly improved vaccine-specific immune responses, restored the immune cell balance in the spleen and increased SCFA concentrations in the cecum. Incubating Caco-2 cells with TOS and 3'-GL in vitro further confirmed their protective effects against DON-induced barrier disruption, supporting immune modulation. Overall, dietary intervention with TOS can attenuate the adverse effects of DON on Th1-mediated immune responses and gut homeostasis. These beneficial properties might be linked to the high levels of 3'-GL in TOS.

Keywords: delayed-type hypersensitivity; deoxynivalenol; human milk oligosaccharides; immune response; mycotoxin; vaccination.

MeSH terms

  • Adaptive Immunity / drug effects*
  • Animals
  • Caco-2 Cells
  • Cecum / drug effects
  • Diet
  • Fatty Acids, Volatile / metabolism
  • Female
  • Food Contamination
  • Humans
  • Influenza, Human / immunology*
  • Intestines / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Milk, Human / chemistry*
  • Mycotoxins / immunology
  • Oligosaccharides / pharmacology*
  • Spleen / drug effects
  • Th1 Cells / metabolism
  • Trichothecenes / immunology*
  • Trisaccharides / pharmacology*
  • Vaccination*
  • Vaccines / immunology

Substances

  • Fatty Acids, Volatile
  • Mycotoxins
  • Oligosaccharides
  • Trichothecenes
  • Trisaccharides
  • Vaccines
  • 3'-galactosyllactose
  • deoxynivalenol