Marrow-derived CD40-positive cells are required for mice to clear Cryptosporidium parvum infection

A R Hayward1, M Cosyns, M Jones

  • 1Department of Pediatrics and the Barbara Davis Childhood Diabetes Center, University of Colorado School of Medicine, Denver, Colorado, USA. anthony.hayward@uchsc.edu

Infection and Immunity
|February 17, 2001
PubMed

Insights

Marrow-derived cells expressing CD40 are sufficient for clearing Cryptosporidium parvum infections. CD40 on intestinal epithelial cells is not sufficient, suggesting a role in effector pathways, not T-cell activation.

Area of Science:

  • Immunology
  • Parasitology
  • Cell Biology

Background:

  • Cryptosporidium parvum infections require CD4+ T cells, MHC class II, and functional CD40-CD154 signaling.
  • CD40 is expressed on immune cells and can be induced on somatic cells, including intestinal epithelial cells.

Purpose of the Study:

  • To investigate whether CD40 expression on marrow-derived cells or intestinal epithelial cells is critical for clearing C. parvum infections.
  • To elucidate the specific role of CD40 in the immune response to C. parvum.

Main Methods:

  • Bone marrow transplantation experiments were conducted using CD40 knockout mice and chimeric models.
  • Mice were infected with C. parvum, and infection clearance, T-cell activation markers (CD69, CD154), and T-cell infiltration were assessed.

Main Results:

  • Chimeric mice with CD40 expressed on marrow-derived cells cleared C. parvum infection.
  • Mice lacking CD40 on intestinal epithelial cells but with functional marrow-derived CD40 cleared the infection.
  • T-cell activation and intestinal infiltration were not dependent on CD40 expression in the recipient cells.

Conclusions:

  • CD40 expression on marrow-derived cells is sufficient for C. parvum infection clearance.
  • CD40 is not essential for T-cell activation or homing in this context but likely contributes to effector mechanisms mediated by immune cells.

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