Protein surface antigens (Ag) I/II and III of Streptococcus mutans have been implicated in protective immunity to dental caries. The objective of this proposal is to identify individual antigenic determinants of these antigens that may be important for inducing immunity without causing potentially harmful side effects. Further aims are to investigate the immunochemical structure and biological function of these antigens, in order to elucidate further the part played by S. mutans in the cariogenic process, and the mechanisms of immunity to it. A panel of monoclonal antibodies to Ags I/II and III will be developed and tested for their reaction with topographically distinct antigenic determinants in an inhibition radioimmunoassay. These will be used to identify antigenic fragments of Ags I/II and III generated by enzymatic and chemical cleavage, and separated by polyacrylamide gel electrophoresis, using """"""""Western Blotting"""""""". Antigens and their fragments will be purified by immunoadsorbent chromatography and analysed chemically for amino acids and carbohydrates. Comparisons will be made between materials obtained from different serotypes of S. mutans, and from S. sanguis and recombinant clones of E. coli expressing S. mutans antigen genes. The purified fragments will also be used in assays of antibodies in the sera and saliva of experimental animals that have been immunized against S. mutans, and of human subjects, in order to examine whether the individual antigenic determinants are relevant to immunity to caries. The monoclonal antibodies (and conventional antisera) will also be used as inhibitors of surface-related and metabolic properties of S. mutans, such as adherence to surfaces, growth and acid production, in order to investigate the physiological functions of Ags I/II and III. The antigens will also be tested directly for their ability to interact with components of saliva.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE006746-06
Application #
3220250
Study Section
Oral Biology and Medicine Study Section (OBM)
Project Start
1984-01-01
Project End
1990-05-31
Budget Start
1989-06-01
Budget End
1990-05-31
Support Year
6
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
School of Medicine & Dentistry
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Zhao, W; Zhao, Z; Russell, M W (2011) Characterization of antigen-presenting cells induced by intragastric immunization with recombinant chimeric immunogens constructed from Streptococcus mutans AgI/II and type I or type II heat-labile enterotoxins. Mol Oral Microbiol 26:200-9
Russell, Michael W; Mestecky, Jiri (2010) Tolerance and protection against infection in the genital tract. Immunol Invest 39:500-25
Mestecky, Jiri; Russell, Michael W (2009) Specific antibody activity, glycan heterogeneity and polyreactivity contribute to the protective activity of S-IgA at mucosal surfaces. Immunol Lett 124:57-62
Liang, Shuang; Hosur, Kavita B; Nawar, Hesham F et al. (2009) In vivo and in vitro adjuvant activities of the B subunit of Type IIb heat-labile enterotoxin (LT-IIb-B5) from Escherichia coli. Vaccine 27:4302-8
Ostberg, K L; Russell, M W; Murphy, T F (2009) Mucosal immunization of mice with recombinant OMP P2 induces antibodies that bind to surface epitopes of multiple strains of nontypeable Haemophilus influenzae. Mucosal Immunol 2:63-73
Mestecky, Jiri; Russell, Michael W; Elson, Charles O (2007) Perspectives on mucosal vaccines: is mucosal tolerance a barrier? J Immunol 179:5633-8
Nawar, Hesham F; Arce, Sergio; Russell, Michael W et al. (2007) Mutants of type II heat-labile enterotoxin LT-IIa with altered ganglioside-binding activities and diminished toxicity are potent mucosal adjuvants. Infect Immun 75:621-33
Liang, Shuang; Wang, Min; Triantafilou, Kathy et al. (2007) The A subunit of type IIb enterotoxin (LT-IIb) suppresses the proinflammatory potential of the B subunit and its ability to recruit and interact with TLR2. J Immunol 178:4811-9
Price, Gregory A; Masri, Heather P; Hollander, Aimee M et al. (2007) Gonococcal transferrin binding protein chimeras induce bactericidal and growth inhibitory antibodies in mice. Vaccine 25:7247-60
Arce, Sergio; Nawar, Hesham F; Muehlinghaus, Gwendolin et al. (2007) In vitro induction of immunoglobulin A (IgA)- and IgM-secreting plasma blasts by cholera toxin depends on T-cell help and is mediated by CD154 up-regulation and inhibition of gamma interferon synthesis. Infect Immun 75:1413-23

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