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Infection and Immunity, May 2001, p. 3255-3263, Vol. 69, No. 5
Department of Cell Biology and Molecular
Genetics, University of Maryland, College Park, Maryland 20742
Received 17 July 2000/Returned for modification 11 August
2000/Accepted 22 February 2001
CD40 ligand (CD40L) is a potent inducer of interleukin-12
(IL-12) production from macrophages and dendritic cells. We show that
combining CD40L with antigen derived from Leishmania is an effective way to preferentially induce type 1 immune responses to the
antigen and to vaccinate mice against subsequent challenge with
virulent organisms. Mice vaccinated in this way had smaller lesions,
with more than 1,000-fold fewer parasites within them. To improve
the efficiency of CD40L-induced immunopotentiation, we attempted to
specifically direct CD40L to macrophages. We developed transfected
cells expressing CD40L and a single Leishmania antigen, gp63. These cells bound efficiently to macrophages and induced robust IL-12 production. Vaccination with these cotransfected cells
provided a significant degree of protection against challenge with
virulent organisms. CD40L was also adsorbed to the surface of virulent
Leishmania. These organisms induced only modest lesions in
genetically susceptible mice, and the lesions had an average of
105-fold fewer organisms within them relative to control
mice. These studies suggest that CD40L could be exploited to improve
vaccines against intracellular pathogens, especially those organisms
that reside within cells expressing CD40 on their surface.
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.5.3255-3263.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Vaccination against the Intracellular Pathogens Leishmania
major and L. amazonensis by Directing CD40 Ligand
to Macrophages
*
Corresponding author. Mailing address: Department of
Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742. Phone: (301) 314-2594. Fax: (301) 314-9489. E-mail: dm268{at}umail.umd.edu.
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