(from the application): The goal of our program is to provide high quality research training in the biomedical investigation of the rheumatic diseases. We have developed a research training environment conducive to the proper nurturing of young scientists interested in the rheumatic diseases. Two pathways are proposed: Training of M.D. rheumatology fellows, and training of Ph.D. scientists. Both will be exposed to basic investigation of a scientific question by hands-on experience and to clinical rheumatology. Our research program is centered on five major areas: 1) Animal models of rheumatic disease; 2) Autoimmunity and tolerance; 3) Inflammation and complement; 4) Immunoregulation and host defense; 5) Receptor signaling. Preceptors with outstanding track records in training and stable funding from 3 distinct units at Washington University are participating. This includes the Rheumatology Division in the Department of Medicine, the Division of Allergy, Immunology, and Rheumatology in the Department of Pediatrics, and the Center for Immunology. Both physician-scientists (M.D. and M.D.-Ph.D.) and basic scientist (Ph.D.) preceptors form the Program faculty who are dedicated to training the next generation of basic scientists interested in the immunobiology of the rheumatic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32AR007279-24
Application #
6171588
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Ader, Deborah N
Project Start
1977-09-30
Project End
2002-04-30
Budget Start
2000-05-01
Budget End
2001-04-30
Support Year
24
Fiscal Year
2000
Total Cost
$224,589
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Kulkarni, Hrishikesh S; Witt, Chad A (2018) Voriconazole in lung transplant recipients - how worried should we be? Am J Transplant 18:5-6
Kulkarni, Hrishikesh S; Elvington, Michelle L; Perng, Yi-Chieh et al. (2018) Intracellular C3 Protects Human Airway Epithelial Cells from Stress-Associated Cell Death. Am J Respir Cell Mol Biol :
Kulkarni, Hrishikesh S; Liszewski, M Kathryn; Brody, Steven L et al. (2018) The complement system in the airway epithelium: An overlooked host defense mechanism and therapeutic target? J Allergy Clin Immunol 141:1582-1586.e1
Hoegl, Sandra; Ehrentraut, Heidi; Brodsky, Kelley S et al. (2017) NK cells regulate CXCR2+ neutrophil recruitment during acute lung injury. J Leukoc Biol 101:471-480
Liszewski, M Kathryn; Elvington, Michelle; Kulkarni, Hrishikesh S et al. (2017) Complement's hidden arsenal: New insights and novel functions inside the cell. Mol Immunol 84:2-9
Elvington, Michelle; Liszewski, M Kathryn; Bertram, Paula et al. (2017) A C3(H20) recycling pathway is a component of the intracellular complement system. J Clin Invest 127:970-981
Schmid, Edward T; Pang, Iris K; Carrera Silva, Eugenio A et al. (2016) AXL receptor tyrosine kinase is required for T cell priming and antiviral immunity. Elife 5:
Elvington, Michelle; Liszewski, M Kathryn; Atkinson, John P (2016) Evolution of the complement system: from defense of the single cell to guardian of the intravascular space. Immunol Rev 274:9-15
Speer, Scott D; Li, Zhi; Buta, Sofija et al. (2016) ISG15 deficiency and increased viral resistance in humans but not mice. Nat Commun 7:11496
Miner, Jonathan J; Diamond, Michael S (2016) Mechanisms of restriction of viral neuroinvasion at the blood-brain barrier. Curr Opin Immunol 38:18-23

Showing the most recent 10 out of 62 publications