We have developed a model of one infectious process in which both arms of the immune system function and, in fact, operate in concert. In the first two years of this grant, we explored in detail the interactions of T cells and B. fragilis. Five areas of fundamental importance have emerged: 1) a soluble, small molecular weight lymphokine (ITF) of splenic phenotypic suppressor T cell origin confers antigenspecific immunity to abcesses, 2) protection in vivo and killing of B. fragilis in vitro require the presence of ITF and complement, 3) a circuit involving at least two suppressor T cells (by phenotype) is involved in immunity to abscesses, 4) an inducer T cell which is phenotypically Ly 1+2+ is necessary for the formation of abscesses, and 5) distinct determinants exist on the B. fragilis capsular polysaccharide for inducing cellular and humoral immunity. Based on these findings, we have evolved a hypothesis which will allow elucidation of a complete immune mechanism for a single infectious process, intraabdominal abscesses. The purpose of the current proposal is to test four components of the hypothetical scheme. These four specific aims include: 1) characterization of the antigenic determinant responsible for humoral and cellular immunity, 2) characterization of the cell types involved in immunity, 3) purification and characterization of the ITF produced by a T cell hybridoma which protects animals against abscesses and 4) in vitro and in vivo definition of the mechanisms of interaction between T cells and the complement system, an interaction which is necessary for protection against abscesses. These types of observations might appear to be unique to the anaerobe, B. fragilis, but hold the potential for a major expansion in the understanding of pathogenesis and host defense. Interactions of this sort have been described previously, but we know of no infectious processes which have been analyzed in this fashion. A number of important bacterial infections lack clear explanations of pathogenesis and immunity. Elucidation of the principles involved in our system may lead to an expanded level of understanding of other infectious diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI022807-05
Application #
3134346
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1985-12-01
Project End
1991-11-30
Budget Start
1989-12-01
Budget End
1991-11-30
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
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Tzianabos, A O; Pantosti, A; Baumann, H et al. (1992) The capsular polysaccharide of Bacteroides fragilis comprises two ionically linked polysaccharides. J Biol Chem 267:18230-5
Tzianabos, A O; Pantosti, A; Baumann, H et al. (1991) Structural characterization of two surface polysaccharides of Bacteroides fragilis. Trans Assoc Am Physicians 104:285-95
Pantosti, A; Tzianabos, A O; Onderdonk, A B et al. (1991) Immunochemical characterization of two surface polysaccharides of Bacteroides fragilis. Infect Immun 59:2075-82
Onderdonk, A B; Cisneros, R L; Crabb, J H et al. (1989) Intraperitoneal host cellular responses and in vivo killing of Bacteroides fragilis in a bacterial containment chamber. Infect Immun 57:3030-7
Kasper, D L; Finberg, R F; Crabb, J et al. (1989) Immune mechanisms in the prevention of intra-abdominal abscess formation. Scand J Infect Dis Suppl 62:29-34
Baker, C J; Rench, M A; Edwards, M S et al. (1988) Immunization of pregnant women with a polysaccharide vaccine of group B streptococcus. N Engl J Med 319:1180-5