Literature DB >> 17804125

Protective immunization against visceral leishmaniasis using Leishmania sterol 24-c-methyltransferase formulated in adjuvant.

Yasuyuki Goto1, Lisa Y Bogatzki, Sylvie Bertholet, Rhea N Coler, Steven G Reed.   

Abstract

We present here the identification and characterization of Leishmania sterol 24-c-methyltransferase (SMT), as well as data on protection of mice immunized with this Ag formulated in MPL-SE. Serological evaluation revealed that SMT is recognized by VL patients. C57BL/6 mice immunized with this vaccine candidate plus MPL-SE showed Ag-specific Th1 immune responses characterized by robust production of IFN-gamma upon specific Ag re-exposure in vitro. Upon challenge with L. infantum, mice immunized with SMT plus MPL-SE showed significant lower parasite burdens in both spleens and livers compared with non-immunized mice or mice injected with adjuvant alone. The results indicate that SMT/MPL-SE can be an effective vaccine candidate for use against VL.

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Year:  2007        PMID: 17804125      PMCID: PMC2077354          DOI: 10.1016/j.vaccine.2007.08.001

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  48 in total

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Journal:  Vaccine       Date:  2001-10-12       Impact factor: 3.641

4.  CD8+ T cells are required for primary immunity in C57BL/6 mice following low-dose, intradermal challenge with Leishmania major.

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Journal:  J Immunol       Date:  2002-04-15       Impact factor: 5.422

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Authors:  E M Carvalho; R Badaró; S G Reed; T C Jones; W D Johnson
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

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  36 in total

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5.  Evaluation of ex vivo human immune response against candidate antigens for a visceral leishmaniasis vaccine.

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6.  Hyperlipidemia offers protection against Leishmania donovani infection: role of membrane cholesterol.

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9.  Protein network prediction and topological analysis in Leishmania major as a tool for drug target selection.

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10.  Structure and dynamics studies of sterol 24-C-methyltransferase with mechanism based inactivators for the disruption of ergosterol biosynthesis.

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