Abstract

The current AADCRC program had its beginning in the AADC program Asthma, Allergy and Autoimmunity (AI10386-19). The goal from the inception of the AADC program in 1971 was to bring the scientific resources of Scripps Clinic and Research Foundation (SCRF), especially in immunology and more recently in molecular biology to bear on the clinical problems of asthma, allergy and autoimmunity. At SCRF, the Division of Allergy and Immunology, the Autoimmune Disease Center, the Department of Immunology and the General Clinical Research Center are combining resources and expertise in this continuing study. In addition, the newly established La Jolla Institute of Allergy and Immunology has joined this program and San Diego State University and the San Diego Unified School District are collaborating in the inner city asthma outreach project. The six projects in the AADCRC program are (1) Autoimmunity and B Cell Epitopes, a study designed to elucidate the nature of B cell epitopes targeted in autoimmune diseases, (2) The Kallikrein-Kinin System in Allergy with emphasis on the regulation of this system in asthma and angioedema. Project 3 is directed at exploring the activation of the arachidonate pathway in aspirin-sensitive asthma. Project 4 is directed at the construction of allergen-specific humans Ts hybridomas with the goal of exploring immunological maneuvers for the suppression of IgE antibody responses in allergic patients. Project 5 proposes to study an IgE-binding protein which has wide tissue distribution and may play a role in mast cell activation and mediator release. Project 6 is an outreach program targeted at grade school students in inner city schools in San Diego with a high proportion of minorities. The objective is to determine the impact of educational and environmental control programs on asthma morbidity. This program unifies expertise in allergy, clinical immunology, basic immunology, biochemistry and molecular biology in an integrated combined approach to continue a long-term research effort on Asthma, Allergy and Autoimmunity.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI032834-04
Application #
2067717
Study Section
Special Emphasis Panel (SRC)
Project Start
1991-09-01
Project End
1996-08-31
Budget Start
1994-09-01
Budget End
1996-08-31
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost

  Institution

Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037

  Publications

Gomi, H; Tagaya, Y; Nakano, T et al. (1994) Antigen-binding glycosylation inhibiting factor from a human T-cell hybridoma specific for bee venom phospholipase A2. Proc Natl Acad Sci U S A 91:2824-8
Feizi, T; Solomon, J C; Yuen, C T et al. (1994) The adhesive specificity of the soluble human lectin, IgE-binding protein, toward lipid-linked oligosaccharides. Presence of the blood group A, B, B-like, and H monosaccharides confers a binding activity to tetrasaccharide (lacto-N-tetraose and lacto-N-ne Biochemistry 33:6342-9
Landberg, G; Tan, E M (1994) Characterization of a DNA-binding nuclear autoantigen mainly associated with S phase and G2 cells. Exp Cell Res 212:255-61
Zuberi, R I; Frigeri, L G; Liu, F T (1994) Activation of rat basophilic leukemia cells by epsilon BP, an IgE-binding endogenous lectin. Cell Immunol 156:1-12
Muro, Y; Tsai, W M; Houghten, R et al. (1994) Synthetic compound peptide simulating antigenicity of conformation-dependent autoepitope. J Biol Chem 269:18529-34
Konstantinov, K N; Shames, B; Izuno, G et al. (1994) Expression of epsilon BP, a beta-galactoside-binding soluble lectin, in normal and neoplastic epidermis. Exp Dermatol 3:9-16
Tan, E M; Muro, Y; Pollard, K M (1994) Autoantibody-defined epitopes on nuclear antigens are conserved, conformation-dependent and active site regions. Clin Exp Rheumatol 12 Suppl 11:S27-31
Imai, H; Fritzler, M J; Neri, R et al. (1994) Immunocytochemical characterization of human NOR-90 (upstream binding factor) and associated antigens reactive with autoimmune sera. Two MR forms of NOR-90/hUBF autoantigens. Mol Biol Rep 19:115-24
Jeng, K C; Frigeri, L G; Liu, F T (1994) An endogenous lectin, galectin-3 (epsilon BP/Mac-2), potentiates IL-1 production by human monocytes. Immunol Lett 42:113-6
Tan, E M (1993) Molecular biology of nuclear autoantigens. Adv Nephrol Necker Hosp 22:213-36

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