This application seeks renewal of a program, currently in its tenth year of support, to train post-doctoral, pediatric physician and non-physician trainees in basic immunology side-by-side in the rich, shared environment of the Department of Immunology at the University of Washington; five positions are requested. This represents a joint venture between the Department of Immunology and the Division of Pediatric Immunology, Infectious Diseases and Rheumatology. Physician and non-physician trainees complement each other: The physician investigators bring to the program unique perspectives derived from direct interaction with patients and laboratory research experience of varying degrees. The non-physician, Ph.D. trainees bring to the program a rich background of didactic and laboratory research experience, but limited familiarity with the potential clinical ramifications of their work. The key quality sought in all trainees is a clear commitment to and outstanding potential for research. Training consists of laboratory research under the mentorship of a member of the training faculty, course work and other informal training experiences for a period of three or more years. A formal course in the responsible conduct of research is included. The ultimate goal of the program is to develop the next generation of investigators, who will make important contributions to our understanding of fundamental immunology and of normal and abnormal immune function relevant to human immunological and infectious diseases. This is a particularly timely goal, since we are now at a juncture when the application of immunological principles derived from fundamental research to human biology and disease is at hand, as witnessed by the advent of programs such as the immune tolerance network, the rational development of new vaccines and other forms of human immunotherapeutics.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI007411-13
Application #
6940762
Study Section
Allergy & Clinical Immunology-1 (AITC)
Program Officer
Prograis, Lawrence J
Project Start
1993-07-01
Project End
2008-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
13
Fiscal Year
2005
Total Cost
$217,922
Indirect Cost
Name
University of Washington
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Thompson, Lucas J; Lai, Jen-Feng; Valladao, Andrea C et al. (2016) Conditioning of naive CD4(+) T cells for enhanced peripheral Foxp3 induction by nonspecific bystander inflammation. Nat Immunol 17:297-303
Mohar, Isaac; Brempelis, Katherine J; Murray, Sara A et al. (2015) Isolation of Non-parenchymal Cells from the Mouse Liver. Methods Mol Biol 1325:3-17
Bell, Bryan D; Kitajima, Masayuki; Larson, Ryan P et al. (2013) The transcription factor STAT5 is critical in dendritic cells for the development of TH2 but not TH1 responses. Nat Immunol 14:364-71
Ziegler, Steven F; Roan, Florence; Bell, Bryan D et al. (2013) The biology of thymic stromal lymphopoietin (TSLP). Adv Pharmacol 66:129-55
Larson, Ryan P; Shafiani, Shahin; Urdahl, Kevin B (2013) Foxp3(+) regulatory T cells in tuberculosis. Adv Exp Med Biol 783:165-80
Roan, Florence; Bell, Bryan D; Stoklasek, Thomas A et al. (2012) The multiple facets of thymic stromal lymphopoietin (TSLP) during allergic inflammation and beyond. J Leukoc Biol 91:877-86
Stromnes, Ingunn M; Fowler, Carla; Casamina, Chanel C et al. (2012) Abrogation of SRC homology region 2 domain-containing phosphatase 1 in tumor-specific T cells improves efficacy of adoptive immunotherapy by enhancing the effector function and accumulation of short-lived effector T cells in vivo. J Immunol 189:1812-25
Sacho, Elizabeth J; Maizels, Nancy (2011) DNA repair factor MRE11/RAD50 cleaves 3'-phosphotyrosyl bonds and resects DNA to repair damage caused by topoisomerase 1 poisons. J Biol Chem 286:44945-51
Lord, James D; Hackman, Robert C; Gooley, Ted A et al. (2011) Blood and gastric FOXP3+ T cells are not decreased in human gastric graft-versus-host disease. Biol Blood Marrow Transplant 17:486-96
Oestreich, Kenneth J; Huang, Albert C; Weinmann, Amy S (2011) The lineage-defining factors T-bet and Bcl-6 collaborate to regulate Th1 gene expression patterns. J Exp Med 208:1001-13

Showing the most recent 10 out of 23 publications