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pubmed-article:16041057pubmed:abstractTextThis study reports the efficacy of a heterologous prime-boost vaccination using DNA and vaccinia viruses (Western Reserve [WR] virus and modified [attenuated] vaccinia virus Ankara [MVA]) expressing the LACK antigen (Leishmania homologue of receptors for activated C kinase) and an intradermal murine infection model employing Leishmania infantum. At 1 month postinfection, vaccinated mice showed high levels of protection in the draining lymph node (240-fold reduction in parasite burden) coupled with significant levels of gamma interferon (20 to 200 ng/ml) and tumor necrosis factor alpha/lymphotoxin (8 to 134 pg/ml). Significant but lower levels of protection (6- to 30-fold) were observed in the spleen and liver. Comparable levels of protection were found for mice boosted with either LACK-WR or LACK-MVA, supporting the use of an attenuated vaccinia virus-based vaccine against human visceral leishmaniasis.lld:pubmed
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pubmed-article:16041057pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:16041057pubmed:articleTitleHeterologous prime-boost vaccination with the LACK antigen protects against murine visceral leishmaniasis.lld:pubmed
pubmed-article:16041057pubmed:affiliationDepartment of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06520-8034, USA.lld:pubmed
pubmed-article:16041057pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16041057pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:16041057pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:16041057pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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