Cellular immune responses are thought to play a major role in immunity to bacterial infections. Bacteroides gingivalis is a gram-negative anaerobic rod that has been isolated from periodontal abscesses, endodontic abscesses and various medical infections and is thought to be an important microorganism in the etiology of human periodontal disease. Since the interactions between host and periodontopathogen that result in abscess formation or resistance to infection are poorly understood, this study proposes to look at these interactions using B. gingivalis in a mouse model. Mice will be immunized with B. gingivalis, or with bacterial extracts obtained by affinity chromatography using monoclonal antibodies conjugated to Sepharose 4B. Following immunization, mice will be challenged intraperitoneally or subcutaneously with viable G. gingivalis. Lymphocyte subpopulations and serum obtained from mice resistant to abscess formation will be used for passive transfer experiments to determine the roles of T cells, T-cell subsets, B cells and immune serum in protection against B. gingivalis. Lymphocyte subpopulations will be obtained using immunofluorescent cell fractionation techniques on an Ortho Cytofluorograf model 50H. Antigen-specific T-cell lines and B-cell lines will be established from immunized mice so that immune responses to B. gingivalis can be tested using homogenous populations of lymphocytes. Both in vivo (passive transfer experiments) and in vitro (blastogenesis, antibody production and adjuvant activity) immune responses will be analysed and compared. Antigen-specific T-cell and B-cell lines will be established from periodontal patients and the in vitro immune reactivity of these cell lines to B. gingivalis will also be analysed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE006880-02
Application #
3220340
Study Section
Oral Biology and Medicine Study Section (OBM)
Project Start
1984-03-01
Project End
1987-02-28
Budget Start
1985-03-01
Budget End
1986-02-28
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
State University of New York at Buffalo
Department
Type
Schools of Dentistry/Oral Hygn
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
Chen, P B; Davern, L B; Katz, J et al. (1996) Host responses induced by co-infection with Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans in a murine model. Oral Microbiol Immunol 11:274-81
Schifferle, R E; Chen, P B; Davern, L B et al. (1993) Modification of experimental Porphyromonas gingivalis murine infection by immunization with a polysaccharide-protein conjugate. Oral Microbiol Immunol 8:266-71
Chen, P B; Davern, L B; Aguirre, A (1991) Experimental Porphyromonas gingivalis infection in nonimmune athymic BALB/c mice. Infect Immun 59:4706-9
Chen, P B; Davern, L B; Neiders, M E et al. (1991) Analysis of in vitro lymphoproliferative responses and antibody formation following subcutaneous injection of Actinobacillus actinomycetemcomitans and Wolinella recta in a murine model. Oral Microbiol Immunol 6:12-6
Chen, P B; Davern, L B; Schifferle, R et al. (1990) Protective immunization against experimental Bacteroides (Porphyromonas) gingivalis infection. Infect Immun 58:3394-400
Mookerjee, B K; Chen, P B; Pauly, J L (1989) IL-2-induced polyclonal proliferation of human peripheral blood lymphocytes: functional and phenotypic characteristics of proliferating cells. Immunology 66:176-82
Neiders, M E; Chen, P B; Suido, H et al. (1989) Heterogeneity of virulence among strains of Bacteroides gingivalis. J Periodontal Res 24:192-8
Chen, P B; Neiders, M E; Millar, S J et al. (1987) Effect of immunization on experimental Bacteroides gingivalis infection in a murine model. Infect Immun 55:2534-7
Kaminsky, S G; Milisauskas, V; Chen, P B et al. (1987) Defective differentiation of natural killer cells in SJL mice. Role of the thymus. J Immunol 138:1020-5
Osur, S L; Lillie, M A; Chen, P B et al. (1987) Elevation of serum IgG levels and normalization of T4/T8 ratio after hepatitis in a patient with common variable hypogammaglobulinemia. J Allergy Clin Immunol 79:969-75

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