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Eur J Immunol ; 31(8): 2338-46, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11477546

ABSTRACT

Prion diseases are caused by conformational alterations in the prion protein (PrP). The immune system has been assumed to be non-responsive to the self-prion protein, therefore, PrP autoimmunity has not been investigated. Here, we immunized various strains of mice with PrP peptides, some selected to fit the MHC class II-peptide binding motif. We found that specific PrP peptides elicited strong immune responses in NOD, C57BL/6 and A/J mice. To test the functional effect of this immunization, we examined the expression of proteinase-K-resistant PrP by a scrapie-infected tumor transplanted to immunized syngeneic A/J mice. PrP peptide vaccination did not affect the growth of the infected tumor transplant, but significantly reduced the level of protease-resistant PrP. Our results demonstrate that self-PrP peptides are immunogenic in mice and suggest that this immune response might affect PrP-scrapie levels in certain conditions.


Subject(s)
Endopeptidase K/metabolism , Peptides/immunology , Peptides/metabolism , PrPSc Proteins/immunology , PrPSc Proteins/metabolism , Scrapie/immunology , Vaccination , Amino Acid Sequence , Animals , Antibody Specificity , Autoimmunity/immunology , Blotting, Western , Cell Division , Cells, Cultured , Female , Histocompatibility Antigens Class II/immunology , Immunoglobulin G/biosynthesis , Immunoglobulin G/immunology , Lymphocyte Activation , Mice , Mice, Inbred A , Mice, Inbred C57BL , Mice, Inbred NOD , Molecular Sequence Data , Neoplasm Transplantation , Neuroblastoma/chemistry , Neuroblastoma/metabolism , Neuroblastoma/pathology , Peptides/chemistry , PrPSc Proteins/chemistry , Scrapie/metabolism , Scrapie/therapy , T-Lymphocytes/cytology , T-Lymphocytes/immunology , Tumor Cells, Cultured
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