Affiliation:
1. Department of Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado 80523
Abstract
ABSTRACT
The importance of CD40, CD80, and CD86 costimulatory molecules in anti-
Leishmania
immune responses has been established in murine models. A role for these costimulatory molecules in human anti-
Leishmania
immune responses was investigated in this study. Autologous macrophages and peripheral blood leukocytes (PBL) were prepared from peripheral blood mononuclear cells of
Leishmania
-naive donors and cultured with or without
Leishmania major
in various combinations. After 7 days of culture, high levels of CD40 and CD86 were expressed on macrophages in the presence or absence of
L. major
. When macrophages were cultured for an additional 7 days with PBL, expression of all three costimulatory molecules was detected. When
L. major
was present in these cultures, the expression of CD80, and to a lesser extent CD40, on macrophages was enhanced. Blockade of CD80, CD86, or both molecules (in the order of greatest effect) in cultures containing macrophages, PBL, and
L. major
significantly inhibited the production of gamma interferon, interleukin-5 (IL-5), and IL-12. Blockade of CD40-CD154 interactions also significantly inhibited production of these cytokines in response to
L. major
. Production of IL-10 was unaltered by the blockade of these costimulatory molecules. Thus, these data suggest that CD40, CD80, and CD86 expression and regulation may significantly impact anti-
Leishmania
immune responses in humans.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
25 articles.
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