Dynamics of Th17 associating cytokines in Cryptosporidium parvum-infected mice

G H Zhao1, Y Q Fang1, U Ryan2

  • 1College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi Province, 712100, People's Republic of China.

Parasitology Research
|November 24, 2015
PubMed

Insights

The study found that interleukin-17 (IL-17) and related cytokines increase in mice with Cryptosporidium parvum infection, suggesting Th17 cells are involved in the immune response to this parasite.

Area of Science:

  • Immunology
  • Parasitology
  • Molecular Biology

Background:

  • Cryptosporidium parvum is an intestinal parasite causing diarrhea in humans and animals.
  • Host immune responses to C. parvum are not fully understood.
  • Interleukin-17 (IL-17) is a pro-inflammatory cytokine implicated in host defense against parasitic infections.

Purpose of the Study:

  • To investigate the role of IL-17 and Th17-associated cytokines in the immune response to C. parvum infection.
  • To examine IL-17 mRNA and protein levels, as well as related cytokine expression, in infected mice.

Main Methods:

  • BALB/c mice were infected with C. parvum and immunosuppressed.
  • Real-time quantitative PCR (qPCR) was used to measure mRNA levels of IL-17 and Th17-related cytokines (TGF-β, IL-6, STAT-3, RORγt, IL-22, TNF-α, IL-23).
  • Enzyme-linked immunosorbent assay (ELISA) was used to determine IL-17 protein levels.

Main Results:

  • Significant increases in IL-17 mRNA and Th17-related cytokine mRNA levels were observed in the gut-associated lymphoid tissue (GALT) and spleen of infected mice.
  • IL-17 protein levels were also significantly elevated in the GALT.
  • These changes were statistically significant (P < 0.05).

Conclusions:

  • Th17 cells and associated cytokines play a significant role in the host's immune response to C. parvum infection.
  • These findings contribute to understanding host-parasite interactions and may inform strategies for managing C. parvum infections, particularly in immunocompromised individuals.