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Infection and Immunity, January 2001, p. 386-391, Vol. 69, No. 1
Department of Medical Zoology, Nagoya City
University Medical School, Nagoya,1 and
Department of Parasitology, Aichi Medical University,
Aichi,2 Japan
Received 21 July 2000/Returned for modification 16 September
2000/Accepted 24 October 2000
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-
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.386-391.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Vaccination with Calpain Induces a Th1-Biased
Protective Immune Response against Schistosoma
japonicum
) by activated
CD4+ T cells. Considering our observation of elevated
expression of inducible nitric oxide synthase mRNA in immunized mice,
r-calpain-induced IFN-
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.
*
Corresponding author. Mailing address: Department of
Medical Zoology, Nagoya City University Medical School, 1 Azakawasumi, Mizuhocho, Mizuhoku, Nagoya 467-8601, Japan. Phone: 81-52-853-8184. Fax: 81-52-842-0149. E-mail:
nohta{at}med.nagoya-cu.ac.jp.
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