Intramuscular immunization with p36(LACK) DNA vaccine induces IFN-gama production but does not protect BALB/c mice against Leishmania chagasi intravenous challenge.
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Date
2005
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Abstract
Acute visceral leishmaniasis is a progressive
disease caused by Leishmania chagasi in South America.
The acquisition of immunity following infection suggests
that vaccination is a feasible approach to protect against this
disease. Since Leishmania homologue of receptors for
activated C kinase (LACK) antigen is of particular interest
as a vaccine candidate because of the prominent role it plays
in the pathogenesis of experimental Leishmania major
infection, we evaluated the potential of a p36(LACK) DNA
vaccine in protecting BALB/c mice challenged with L.
chagasi. In this study, mice received intramuscular (i.m.) or
subcutaneous (s.c.) doses of LACK DNA vaccine. We
evaluated the production of vaccine-induced cytokines and
whether this immunization was able to reduce parasite load
in liver and spleen. We detected a significant production of
interferon gamma by splenocytes from i.m. vaccinated mice
in response to L. chagasi antigen and to rLACK protein.
However, we did not observe a reduction in parasite load
neither in liver nor in the spleen of vaccinated animals. The
lack of protection observed may be explained by a significant
production of IL-10 induced by the vaccine.
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Lack
Citation
SILVA, E. A. M. da et al. Intramuscular immunization with p36(LACK) DNA vaccine induces IFN-gama production but does not protect BALB/c mice against Leishmania chagasi intravenous challenge. Parasitology Research, v. 98, n.1, p. 67-74, 2005. Disponível em: <http://link.springer.com/article/10.1007%2Fs00436-005-0008-8>. Acesso em: 20 jan. 2017.