The purpose of the Integrated Immunology Training Program (IITP) at the University of Texas Southwestern Medical Center (UT Southwestern) is to provide comprehensive training for graduate students, medical scientist trainees, and post-doctoral fellows for cutting-edge immunology-related research careers. The goal is to prepare exceptionally qualified individuals for the investigation and resolution of such significant immune-related problems as autoimmune diseases, allergies, infectious diseases, and immunodeficiencies. These goals will be achieved by a combination of rigorous and intellectually challenging didactic immunology courses, cutting-edge research projects, research presentations, a qualifying exam, seminars, journal clubs, and career development programs. The training program includes the selection IITP faculty who are distributed among thirteen, distinct departments and/or centers (Immunology, Microbiology, Pathology, Cancer Immunobiology, Internal Medicine-Rheumatology, Internal Medicine-Infectious Diseases, Biochemistry, Molecular Biology, Pediatrics, Neurology, Nephrology, Dermatology, Ophthalmology). These faculty are selected based on their leadership role in either a) developing new immunology courses and/or curriculums, b) directing an immunology course, and c) strong commitment in training students and post- doctoral fellows. The IITP is supported by 11 administrative committees that function as part of the program in immunology. Advanced training in immunology is essential for responding to global issues of re-emerging infectious diseases, an aging population suffering the ills of autoimmune diseases, and the recent unfortunate international threat of bioterrorism. The strong didactic courses offered by the Immunology Program provide in-depth coverage of these issues. The research tracts of the IITP faculty are responding to these global challenges. These goals continue to be achieved, as evidenced by the previous trainees that have completed the training and have continued in academia and industry.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI005284-35
Application #
8320939
Study Section
Allergy & Clinical Immunology-1 (AITC)
Program Officer
Prograis, Lawrence J
Project Start
1980-07-01
Project End
2014-08-31
Budget Start
2012-09-01
Budget End
2014-08-31
Support Year
35
Fiscal Year
2012
Total Cost
$361,775
Indirect Cost
$27,673
Name
University of Texas Sw Medical Center Dallas
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
A?aç, Didem; Estrada, Leonardo D; Maples, Robert et al. (2018) The ?2-adrenergic receptor controls inflammation by driving rapid IL-10 secretion. Brain Behav Immun 74:176-185
Ottens, Kristina; Hinman, Rochelle M; Barrios, Evan et al. (2018) Foxo3 Promotes Apoptosis of B Cell Receptor-Stimulated Immature B Cells, Thus Limiting the Window for Receptor Editing. J Immunol 201:940-949
Mar, Katrina B; Rinkenberger, Nicholas R; Boys, Ian N et al. (2018) LY6E mediates an evolutionarily conserved enhancement of virus infection by targeting a late entry step. Nat Commun 9:3603
Cohee, Lauren M; Chilombe, Moses; Ngwira, Andrew et al. (2018) Pilot Study of the Addition of Mass Treatment for Malaria to Existing School-Based Programs to Treat Neglected Tropical Diseases. Am J Trop Med Hyg 98:95-99
Deason, Krystin; Troutman, Ty Dale; Jain, Aakanksha et al. (2018) BCAP links IL-1R to the PI3K-mTOR pathway and regulates pathogenic Th17 cell differentiation. J Exp Med 215:2413-2428
Richardson, R Blake; Ohlson, Maikke B; Eitson, Jennifer L et al. (2018) A CRISPR screen identifies IFI6 as an ER-resident interferon effector that blocks flavivirus replication. Nat Microbiol 3:1214-1223
Randesi, Matthew; Levran, Orna; Correa da Rosa, Joel et al. (2017) Association of Variants of Arginine Vasopressin and Arginine Vasopressin Receptor 1A With Severe Acetaminophen Liver Injury. Cell Mol Gastroenterol Hepatol 3:500-505
Franco, Luis H; Nair, Vidhya R; Scharn, Caitlyn R et al. (2017) The Ubiquitin Ligase Smurf1 Functions in Selective Autophagy of Mycobacterium tuberculosis and Anti-tuberculous Host Defense. Cell Host Microbe 21:59-72
(2017) Removal Notice. Mult Scler 23:NP1
Yu, Mengxiao; Zhou, Chen; Liu, Li et al. (2017) Interactions of Renal-Clearable Gold Nanoparticles with Tumor Microenvironments: Vasculature and Acidity Effects. Angew Chem Int Ed Engl 56:4314-4319

Showing the most recent 10 out of 102 publications