Expulsion of the gastrointestinal cestode, Hymenolepis diminuta by tolerant rats: evidence for mediation by a Th2 type immune enhanced goblet cell hyperplasia, increased mucin production and secretion

Parasite Immunol. 2007 Jan;29(1):11-21. doi: 10.1111/j.1365-3024.2006.00908.x.

Abstract

The processes underlying expulsion of Hymenolepis diminuta in rats are not known. Expression levels of mRNAs of several cytokines revealed a Th2 response that differed between worm infection levels. IL-4 protein levels decreased while IL-13 levels increased in a 50-worm infection by 30 dpi; the converse was seen with a five-worm infection. A negative correlation was found between IL-4 or IL-13 mRNA expression and worm biomass, between IL-13 protein levels and worm number or worm biomass, and between IL-4 protein levels and worm biomass in 50-worm infections. A negative correlation between IL-4 mRNA or protein expression and worm biomass was observed with five-worm infections. A strong correlation between Muc2 mRNA expression and decreased worm number or biomass in a 50-worm infection was observed. Muc2 protein, goblet cell numbers and mucin decreased in a 50-worm infection by 20 days post-infection. These changes were not seen with five-worm infections where worms are not expelled. The data show that rats infected with 50 H. diminuta mount a Th2 response leading to high levels of IL-13, increased goblet cell numbers and increased mucin2 production and release. The mucus traps the worms, which are progressively expelled from the small intestine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Goblet Cells / parasitology*
  • Goblet Cells / pathology
  • Hymenolepiasis / immunology*
  • Hymenolepis / immunology*
  • Hyperplasia
  • Intestines / immunology
  • Mucins / metabolism*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • STAT6 Transcription Factor
  • Th2 Cells / immunology*
  • Th2 Cells / parasitology

Substances

  • Mucins
  • RNA, Messenger
  • STAT6 Transcription Factor
  • Stat6 protein, mouse