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Vaccine ; 17(9-10): 1091-9, 1999 Mar 05.
Article in English | MEDLINE | ID: mdl-10195619

ABSTRACT

DNA molecules complexed with an asialoglycoprotein-polycation conjugate, consisting of asialoorosomucoid (ASOR) coupled to poly-L-lysine, can enter hepatocytes which bear receptors for ASOR. We used this receptor-mediated DNA delivery system to deliver plasmid DNA encoding glycoprotein D (gD) of herpes simplex virus type 1 to ASOR-positive cells. Maximum expression of gD protein was seen at 3 days after injection of this preparation in approximately 13% of cells from BALB/c mice [hepatocytes from mice injected intravenously (i.v.) or peritoneal exudate cells from mice injected intraperitoneally (i.p.)]. In comparison with mice injected with either the plasmid vector alone or the gD-containing plasmid uncomplexed to ASOR, mice immunized with gD-containing plasmid complexed with ASOR-poly-L-lysine induced marked antigen-specific CTL responses. BALB/c mice immunized with gD-DNA developed a T-cell-mediated CTL response against target cells expressing gD and MHC class II glycoproteins, but not against cells expressing only gD and MHC class I molecules. In C3H mice, gD-DNA induced a T-cell-mediated CTL response against target cells expressing gD and class I MHC molecules. Serum anti-gD antibody in low titers were produced in both strains of mice. DNA complexed with ASOR-poly-L-lysine induced CTL responses in mice.


Subject(s)
Antibodies, Viral/biosynthesis , Asialoglycoproteins/immunology , Hemagglutinins, Viral/immunology , Orosomucoid/analogs & derivatives , Polylysine/immunology , Simplexvirus/immunology , T-Lymphocytes, Cytotoxic/immunology , Vaccination/methods , Viral Envelope Proteins/immunology , Animals , Asialoglycoprotein Receptor , Asialoglycoproteins/metabolism , CD4 Antigens/analysis , Enzyme-Linked Immunosorbent Assay , Female , Liver/cytology , Liver/immunology , Mice , Mice, Inbred BALB C , Mice, Inbred C3H , Orosomucoid/immunology , Orosomucoid/metabolism , Plasmids , Polylysine/metabolism , Receptors, Cell Surface/metabolism , Transfection , Viral Envelope Proteins/biosynthesis
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