Affiliation:
1. Department of Medical Zoology, Nagoya City University Medical School, Nagoya,1 and
2. Department of Parasitology, Aichi Medical University, Aichi,2 Japan
Abstract
ABSTRACT
A large subunit of calpain, a calcium-activated neutral proteinase, from
Schistosoma japonicum
was cloned and expressed in
Escherichia coli
. When BALB/c mice were immunized with purified recombinant calpain (r-calpain) emulsified in complete Freund's adjuvant, a significant reduction in the number of recovered worms and also in egg production per female worm was observed
(P
< 0.01). Spleen cells of the immunized mice showed enhanced production of gamma interferon (IFN-γ) by activated CD4
+
T cells. Considering our observation of elevated expression of inducible nitric oxide synthase mRNA in immunized mice, r-calpain-induced IFN-γ seemed to upregulate the production of nitric oxide by macrophages and subsequently mediated the killing of schistosomulae in the lung. On the other hand, spleen cells of immunized mice showed only faint interleukin-4 production in response to r-calpain in vitro, suggesting that immunization with r-calpain alters the Th1-Th2 balance in murine hosts even during a Th2-promoting
S. japonicum
infection. Furthermore, histopathological study of the livers of immunized mice showed that granulomas formed around eggs were diminished in both size and number. Egg production by female worms was clearly decreased in immunized mice, suggesting that r-calpain also has antifecundity effects. Taken together, these results point to
S. japonicum
calpain as a potential vaccine candidate for both worm killing and disease prevention, possibly through the induction of a strong Th1-dominant environment in immunized mice.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
52 articles.
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