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Infect Immun ; 68(8): 4416-21, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10899838

ABSTRACT

The protozoan parasite Entamoeba histolytica causes extensive morbidity and mortality through intestinal infection and amebic liver abscess. Here we show that immunization of gerbils with a single keyhole limpet hemocyanin-coupled 25-mer peptide derived from the 170-kDa subunit of the E. histolytica galactose-binding adhesin is sufficient to confer substantial protection against experimentally induced amebic liver abscesses. Vaccination provided total protection in 5 of 15 immunized gerbils, and abscesses were significantly smaller (P < 0.01) in the remaining vaccinated animals. The degree of protection correlated with the titer of antibodies to the peptide, and results of passive transfer experiments performed with SCID mice were consistent with a role for antibodies in protection. In addition, parenteral or oral vaccination of gerbils with 13-amino-acid subfragments of the peptide N-terminally fused to the B subunit of cholera toxin also significantly inhibited liver abscess formation (P < 0.05). These data indicate that small peptides derived from the galactose-binding adhesin administered by the parenteral or oral route can provide protection against amebic liver abscess and should be considered as components of a subunit vaccine against invasive amoebiasis.


Subject(s)
Lectins/therapeutic use , Liver Abscess, Amebic/prevention & control , Membrane Glycoproteins/therapeutic use , Peptide Fragments/therapeutic use , Protozoan Proteins/therapeutic use , Protozoan Vaccines/therapeutic use , Vaccination , Adjuvants, Immunologic , Administration, Oral , Animals , Cholera Toxin/genetics , Cholera Toxin/immunology , Cysteine , Female , Gerbillinae , Hemocyanins , Immunization, Passive , Lectins/genetics , Lectins/immunology , Membrane Glycoproteins/genetics , Membrane Glycoproteins/immunology , Mice , Mice, SCID , Peptide Fragments/genetics , Peptide Fragments/immunology , Protozoan Proteins/genetics , Protozoan Proteins/immunology , Protozoan Vaccines/genetics , Protozoan Vaccines/immunology , Recombinant Fusion Proteins/immunology , Recombinant Fusion Proteins/therapeutic use
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