The proposed Center Grant is a request for continued CIRID funding of an ongoing Center for Interdisciplinary Studies of Immunology at Georgetown. The Center exists as a functionally recognized unit of the University and has integrated programs in research, education and patient care, as well as in community, outreach, technology transfer and education. The overall proposed program project consists of senior investigators representing basic science and clinical disciplines (pediatrics, medicine, neurology, biochemistry, microbiology, biostatistics, and community medicine) all of whom have pooled their expertise and resources in the present CIRID grant proposal. The present proposal has been significantly revised and has been prepared as a program project grant and includes five interrelated, interdependent research projects. Four of the project (1-4) interact around a central unifying theme of maturational immunologic processes in the developing host and their role in antimicrobial host defense. The broad hypothesis to be examined is that deficiency or impairment in development in any of a number of nonspecific and specific immunologic parameters can lead to immunologic compromise and predispose the developing host to severe infection and disease. The projects range from studies of the development of phagocytic function in the neonate (Project 1), structural and functional studies of the third component of complement (Project 2), developmental studies of the secretory IgA system (Project 3), studies of the developing immune system on responses to viral and myelin antigens (Project 4); a fifth project community outreach technology transfer and education includes a pediatric asthma patient education project utilizing self-management techniques.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center (P50)
Project #
1P50AI026821-01
Application #
3105094
Study Section
Allergy, Immunology, and Transplantation Research Committee (AITC)
Project Start
1988-09-01
Project End
1993-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
1
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Georgetown University
Department
Type
Schools of Medicine
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Gowda, D C; Glushka, J; Halbeek Hv et al. (2001) N-linked oligosaccharides of cobra venom factor contain novel alpha(1-3)galactosylated Le(x) structures. Glycobiology 11:195-208
Cohn, M L; Robinson, E D; Thomas, D et al. (1996) T cell responses to the paramyxovirus simian virus 5: studies in multiple sclerosis and normal populations. Pathobiology 64:131-5
Vogel, C W; Bredehorst, R; Fritzinger, D C et al. (1996) Structure and function of cobra venom factor, the complement-activating protein in cobra venom. Adv Exp Med Biol 391:97-114
Gowda, D C; Petrella, E C; Raj, T T et al. (1994) Immunoreactivity and function of oligosaccharides in cobra venom factor. J Immunol 152:2977-86
Cohn, M L; Robinson, E D; Faerber, M et al. (1994) Measles vaccine failures: lack of sustained measles-specific immunoglobulin G responses in revaccinated adolescents and young adults. Pediatr Infect Dis J 13:34-8
Fritzinger, D C; Bredehorst, R; Vogel, C W (1994) Molecular cloning and derived primary structure of cobra venom factor. Proc Natl Acad Sci U S A 91:12775-9
Fritzinger, D C; Petrella, E C; Connelly, M B et al. (1992) Primary structure of cobra complement component C3. J Immunol 149:3554-62
Gowda, D C; Schultz, M; Bredehorst, R et al. (1992) Structure of the major oligosaccharide of cobra venom factor. Mol Immunol 29:335-42