Infectious diseases pose a major threat to public health both in the United States and world-wide. Respiratory viruses such as avian influenza have the potential to develop pandemics and kill millions of people. Bacterial pathogens are developing resistance to current antibiotics, resulting in major epidemics. Newly emerging pathogens such as Human Immunodeficiency Virus are rampant in many countries of the world with devastating consequences. In addition, there is the threat that infectious agents will be developed as bioterrorist weapons. In order to meet this challenge there is a need for the training of creative young scientists capable of integrating basic molecular and cellular immunology with infectious disease research. The goal of this proposed Training Program is to produce well-qualified new investigators capable of establishing vigorous independent research programs in infectious disease immunology. Trudeau Institute is an ideal training environment, providing access to a collaborative group of world class scientists with active programs in a variety of well-developed infectious disease models. The research emphasis at the Institute is to address challenging problems in the immunology of infectious disease through a deep mechanistic understanding of the functioning of the immune system. The training faculty are well-funded, established investigators in the field of infectious disease immunology and have an extensive publication record. Importantly, Trudeau Institute has an excellent track record in the training of successful young investigators. The foundation of the training program is intensive laboratory-based research that will foster a creative approach to the design of research strategies and encourage critical analytical thinking. Trainees will have access to state of the art research technologies through the well-developed Institutional cores, including flow cytometry, molecular biology and imaging. In addition, the Institute provides modern laboratory and animal space for studying a variety of infectious diseases. The trainees benefit greatly from the highly collaborative environment at the Institute. As an integral part of the program, the trainees will attend regular seminars by Institutional and external speakers, will regularly present their research both at the Trudeau Institute and at regional and national meetings, will acquire experience in grant writing, and will acquire experience in management and directing the research projects of visiting college summer students. The training period will be 3 years in length. As a result of this extensive and well-rounded training program, trainees will be positioned to establish successful, independent research careers in immunology and infectious disease.

Public Health Relevance

Infectious diseases pose a world-wide threat to human health. Biomedical research is essential to increase our understanding of the body's immune system, in order to develop ways to treat and prevent disease. Therefore an important priority is the in-depth training of new scientists who can carry out vigorous research programs to meet the increasing global challenge.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI049823-13
Application #
8471042
Study Section
Allergy & Clinical Immunology-1 (AITC)
Program Officer
Prograis, Lawrence J
Project Start
2001-07-01
Project End
2016-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
13
Fiscal Year
2013
Total Cost
$163,639
Indirect Cost
$12,121
Name
Trudeau Institute, Inc.
Department
Type
DUNS #
020658969
City
Saranac Lake
State
NY
Country
United States
Zip Code
12983
Vomhof-DeKrey, Emilie E; Yates, Jennifer; Hägglöf, Thomas et al. (2015) Cognate interaction with iNKT cells expands IL-10-producing B regulatory cells. Proc Natl Acad Sci U S A 112:12474-9
Koroleva, Ekaterina P; Halperin, Sydney; Gubernatorova, Ekaterina O et al. (2015) Citrobacter rodentium-induced colitis: A robust model to study mucosal immune responses in the gut. J Immunol Methods 421:61-72
Lynch, Lydia; Michelet, Xavier; Zhang, Sai et al. (2015) Regulatory iNKT cells lack expression of the transcription factor PLZF and control the homeostasis of T(reg) cells and macrophages in adipose tissue. Nat Immunol 16:85-95
Ray, Aurelie A; Fountain, Jeffrey J; Miller, Halli E et al. (2015) IL12R?1?TM is a secreted product of il12rb1 that promotes control of extrapulmonary tuberculosis. Infect Immun 83:560-71
Macho-Fernandez, E; Koroleva, E P; Spencer, C M et al. (2015) Lymphotoxin beta receptor signaling limits mucosal damage through driving IL-23 production by epithelial cells. Mucosal Immunol 8:403-13
Freeman, Michael L; Burkum, Claire E; Cookenham, Tres et al. (2014) CD4 T cells specific for a latency-associated ?-herpesvirus epitope are polyfunctional and cytotoxic. J Immunol 193:5827-34
Sell, Stewart; Guest, Ian; McKinstry, K Kai et al. (2014) Intraepithelial T-cell cytotoxicity, induced bronchus-associated lymphoid tissue, and proliferation of pneumocytes in experimental mouse models of influenza. Viral Immunol 27:484-96
Amiel, Eyal; Everts, Bart; Fritz, Daniel et al. (2014) Mechanistic target of rapamycin inhibition extends cellular lifespan in dendritic cells by preserving mitochondrial function. J Immunol 193:2821-30
Freeman, Michael L; Roberts, Alan D; Burkum, Claire E et al. (2014) Promotion of a subdominant CD8 T cell response during murine gammaherpesvirus 68 infection in the absence of CD4 T cell help. J Virol 88:7862-9
Blackman, M A; Yates, J L; Spencer, C M et al. (2014) The Yin and Yang of inflammation. Curr Mol Med 14:1238-43

Showing the most recent 10 out of 52 publications