The purpose of the research is to determine the structure and function of Fc receptors foR IgE on lymphocytes and monocytes/macrophages. 1. Lymphocytes of patients with allergies to pollen will be analyzed for Fc eta receptors (Fc eta R) positive cells over a year period, before, during and after the grass pollen season. The lymphocytes will be cultured and the IgE produced in vitro measured employing unfractionated and Fc eta R depleted or enriched cells. 2. Monocytes will be purified from patients with allergic disease and studied for Fc eta R positive cells. It will be determined if phagocytosis of IgE coated target cells will cause release of slow reacting substance of anaphylaxis (SRS-A) from monocytes. 3. Rat alveolar and peritoneal macrophages will be analyzed for their ability to form rosettes with red cells coated with rat myeloma proteins of all classes and subclasses. Rat alveolar macrophages were shown to have Fc eta R and will be tested for release of SRS-A after interaction with aggregated IgE myeloma proteins. 4. The numbers of Fc eta R positive lymphocytes (both T and B cells) and macrophages will be determined in rats infected with Nippostronglyus brasiliensis parasites in various lymphoid organs. The number of receptors on these cells will be quantitated by measuring binding of radiolabeled IgE to isolated cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI010734-14
Application #
3124797
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1977-01-01
Project End
1988-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
14
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
San Diego
State
CA
Country
United States
Zip Code
92037
Plett, P Artur; Sampson, Carol H; Chua, Hui Lin et al. (2015) The H-ARS Dose Response Relationship (DRR): Validation and Variables. Health Phys 109:391-8
Roth, R; Spiegelberg, H L (1996) Activation of cloned human CD4+ Th1 and Th2 cells by blood dendritic cells. Scand J Immunol 43:646-51
Beck, L; Roth, R; Spiegelberg, H L (1996) Comparison of monocytes and B cells for activation of human T helper cell subsets. Clin Immunol Immunopathol 78:56-60
Azmi, F H; Lucas, A H; Spiegelberg, H L et al. (1995) Human immunoglobulin M paraproteins cross-reactive with Neisseria meningitidis group B polysaccharide and fetal brain. Infect Immun 63:1906-13
Spiegelberg, H L; Beck, L; Stevenson, D D et al. (1994) Recognition of T cell epitopes and lymphokine secretion by rye grass allergen Lolium perenne I-specific human T cell clones. J Immunol 152:4706-11
Ninomiya, C; Spiegelberg, H L (1992) IL-4 and transforming growth factor-beta suppress human immunoglobulin secretion in vitro by surface IgD- B cells. Clin Exp Immunol 89:261-8
Spiegelberg, H L (1991) Fc epsilon R2/CD23: its discovery and possible functions. Monogr Allergy 29:1-8
Spiegelberg, H L; O'Connor, R D; Falkoff, R J et al. (1991) Interleukin-4 induced IgE and IgG4 secretion by B cells from atopic dermatitis patients. Int Arch Allergy Appl Immunol 94:181-3
Spiegelberg, H L; Falkoff, R J; O'Connor, R D et al. (1991) Interleukin-2 inhibits the interleukin-4-induced human IgE and IgG4 secretion in vivo. Clin Exp Immunol 84:400-5
Spiegelberg, H L (1990) Fc receptors for IgE and interleukin-4 induced IgE and IgG4 secretion. J Invest Dermatol 94:49S-52S

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