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Relationship between neutrophil infiltration and tissue eosinophilia in the rat

R M Cook1, N R Musgrove, H Smith

  • 1Beecham Pharmaceuticals Research Division, Epsom, Surrey, UK.

International Archives of Allergy and Applied Immunology
|January 1, 1988
PubMed

Insights

Infection with Mesocestoides corti parasite increases immune cells in rats. Neutrophil infiltration into the peritoneum is impaired during this parasitic infection, suggesting a compromised inflammatory response.

Area of Science:

  • Parasitology
  • Immunology
  • Cellular Biology

Background:

  • Parasitic infections trigger complex immune responses.
  • Understanding immune cell dynamics is crucial for host defense.
  • Mesocestoides corti is a model parasite for studying host-pathogen interactions.

Purpose of the Study:

  • To investigate the impact of Mesocestoides corti infection on circulating and peritoneal immune cell populations in rats.
  • To examine the effect of parasitic infection on neutrophil recruitment to the peritoneal cavity in response to glycogen challenge.

Main Methods:

  • Rats were infected with Mesocestoides corti.
  • Blood and peritoneal lavage fluid were collected at various time points post-infection.
  • Immune cell counts (neutrophils, eosinophils, mononuclear cells) were determined.
  • Glycogen was administered intraperitoneally to assess neutrophil chemotaxis.

Main Results:

  • Mesocestoides corti infection led to a significant increase in blood neutrophils, eosinophils, and mononuclear cells, peaking at day 11.
  • Elevated eosinophils and mononuclear cells were observed in the peritoneal cavity up to day 81 post-infection.
  • Glycogen induced transient neutrophilia in blood.
  • Peritoneal neutrophil recruitment following glycogen challenge was impaired in rats infected for 24 days, but not 81 days.

Conclusions:

  • Mesocestoides corti infection alters host immune cell profiles.
  • Neutrophil infiltration into the peritoneal cavity is suppressed during a specific phase of this parasitic infection.
  • The findings suggest that the inflammatory response, particularly neutrophil recruitment, can be impaired in the presence of eosinophil-driven inflammation.

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