Affiliation:
1. Departments of Pediatrics and Immunology and the Barbara Davis Childhood Diabetes Center, University of Colorado School of Medicine, Denver, Colorado
Abstract
ABSTRACT
To clear a
Cryptosporidium parvum
infection, mice need CD4
+
T cells, major histocompatibility complex class II, and an intact CD40-CD154 signaling pathway. CD40 is constitutively expressed on marrow-derived cells such as dendritic cells and B lymphocytes and is induced by gamma interferon (IFN-γ) on most somatic cells. To determine whether the CD40 needed to clear a
C. parvum
infection has to be on marrow-derived mononuclear cells or on the epithelial cells that normally harbor the parasite, we transplanted CD40
−/−
mice with CD40
+/−
bone marrow and then infected them with
C. parvum
. These chimeras cleared the
C. parvum
infection, while CD40
+/−
controls transplanted with CD40
−/−
marrow cells remained infected. CD40 expression on marrow-derived cells therefore suffices for a
C. parvum
infection to be cleared, while CD40 expression on intestinal epithelial cells is not sufficient. There was no difference between the acquisition of CD69 and CD154 by mesenteric lymph node T cells of
C. parvum
-infected animals with intact or disrupted CD40-CD154 pathways. CD4 T cells entered the intestinal laminae propriae of
C. parvum
-infected animals whether or not the CD40 genes of these recipients were intact. These results suggest that, for a
C. parvum
infection to be cleared, CD40 is not necessary for T-cell activation but may instead contribute to an effector pathway of marrow-derived cells.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
28 articles.
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