Liposome potentiation of humoral immune response to lipopolysaccharide and O-polysaccharide antigens of Brucella abortus

• Published in: Immunology Vol. 77; no. 1; pp. 123 - 128
• Main Authors: WONG, J. P, CHERWONOGRODZKY, J. W, DI NINNO, V. L, STADNYK, L. L, KNODEL, M. H
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell 01.09.1992
• Subjects: Adjuvants, Immunologic; Animals; Antibodies, Bacterial - biosynthesis; Antigens, Bacterial - immunology; Bacteriology; Biological and medical sciences; Brucella abortus; Brucella abortus - immunology; Brucella Vaccine - immunology; Dose-Response Relationship, Immunologic; Female; Fundamental and applied biological sciences. Psychology; Immunoglobulin G - biosynthesis; Immunoglobulin M - biosynthesis; Lipopolysaccharides - immunology; Liposomes - immunology; Mice; Mice, Inbred BALB C; Microbiology; Polysaccharides, Bacterial - immunology; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies; Encapsulation; Immune response; Rodentia; Liposome; Brucella abortus; Vertebrata; Mammalia; Brucellaceae; Immunogenicity; Mouse; Animal; Lipopolysaccharide; Bacteria; Polysaccharide; Humoral immunity
• ISSN: 0019-2805; 1365-2567

Liposomes were evaluated for their effectiveness as vaccine carriers in the potentiation of the mouse humoral response to the lipopolysaccharide (LPS) and O-polysaccharide (OPS) antigens of Brucella abortus. LPS and OPS were extracted from a pathogenic strain of B. abortus and were encapsulated within multilamellar vesicles. Groups of mice, immunized with liposome-encapsulated and free LPS or OPS, were bled weekly and the specific IgM and IgG levels in the sera were determined by an indirect fluorogenic enzyme-linked immunosorbent assay. Humoral response to these antigens were found to be dose-dependent. Mice immunized with LPS and OPS encapsulated within liposomes were found to have significantly higher IgG levels than mice immunized with free LPS and OPS. In addition, the antibody levels in mice that were immunized with liposome-encapsulated LPS and OPS were more sustained and remained at elevated levels--even after 5 weeks post immunization. As expected, OPS was found to be less immunogenic than LPS, but multiple injections of OPS encapsulated within liposomes greatly improved the immunogenicity. These results indicate that the humoral response to LPS and OPS of B. abortus can be enhanced when these antigens are encapsulated within liposomes.