Understanding the immune system and how it can be manipulated has formed the basis of new technologies, diagnostic tools, and safer, more effective therapies for many medical conditions. Thus, it is very important to train a new generation of young scientists to understand and harness the power of immunity. This is a competitive renewal application for years 16-21 of a training program supporting students pursuing doctoral studies in basic and translational immunology at The University of Iowa. A diversity of areas of immunology available to students is a strength of the program. The goal of the Interdisciplinary Graduate Program in Immunology is to develop the capabilities of students to become successful independent investigators in a variety of careers in basic and applied immunology. The major focus of training is intensive laboratory research conducted under the guidance and mentorship of outstanding faculty immunologists. Complementary aspects include coursework that stresses hypothesis generation and critical analysis skills, a rigorous research-oriented comprehensive examination, training in ethical issues facing scientists, teaching experience, and ample opportunities to gain proficiency in scientific writing and speaking. Students are selected without regard for any characteristics other than their potential as scientists, and are drawn from pools of applicants seeking the Ph.D. in Immunology, the M.D./Ph.D. combined degree, and initially undecided students who select an area of focus at the end of the first year of graduate study. Thirty-two Program faculty are divided into 4 categories. Experienced Mentor/Mentor faculty are active, productive researchers who have successfully trained Ph.D. students (EM) or have trained fellows, but not yet graduate students (M). New Mentors (NM) are junior faculty with appropriate training, and Resource Faculty (R) do not serve as dissertation advisors, but are valuable to the training program in teaching and committee service. How each of these categories of faculty contribute to the program and participate in graduate training is described in detail in the proposal. Information included documents faculty qualifications, student progress, administrative structure of the program, and the detailed training plan for our students. We continue to revise and optimize our Program to best meet the needs of student scientific careers and the diverse scientific workforce of the future. This grant is critical to support our continuing efforts in training predoctoral students from diverse backgrounds for independent careers as immunologists, and also to providing geographic diversity in graduate training in immunology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI007485-18
Application #
8296673
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Prograis, Lawrence J
Project Start
1995-08-01
Project End
2015-07-31
Budget Start
2012-08-01
Budget End
2013-07-31
Support Year
18
Fiscal Year
2012
Total Cost
$219,881
Indirect Cost
$14,383
Name
University of Iowa
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Freedman, Samantha N; Shahi, Shailesh K; Mangalam, Ashutosh K (2018) The ""Gut Feeling"": Breaking Down the Role of Gut Microbiome in Multiple Sclerosis. Neurotherapeutics 15:109-125
Gorman, Jacob V; Colgan, John D (2018) Acute stimulation generates Tim-3-expressing T helper type 1 CD4 T cells that persist in vivo and show enhanced effector function. Immunology 154:418-433
Carlin, Lindsey E; Hemann, Emily A; Zacharias, Zeb R et al. (2018) Natural Killer Cell Recruitment to the Lung During Influenza A Virus Infection Is Dependent on CXCR3, CCR5, and Virus Exposure Dose. Front Immunol 9:781
Jensen, Isaac J; Sjaastad, Frances V; Griffith, Thomas S et al. (2018) Sepsis-Induced T Cell Immunoparalysis: The Ins and Outs of Impaired T Cell Immunity. J Immunol 200:1543-1553
Zacharias, Zeb R; Ross, Kathleen A; Hornick, Emma E et al. (2018) Polyanhydride Nanovaccine Induces Robust Pulmonary B and T Cell Immunity and Confers Protection Against Homologous and Heterologous Influenza A Virus Infections. Front Immunol 9:1953
Hornick, Emma E; Banoth, Balaji; Miller, Ann M et al. (2018) Nlrp12 Mediates Adverse Neutrophil Recruitment during Influenza Virus Infection. J Immunol 200:1188-1197
Nada, Mohanad H; Wang, Hong; Workalemahu, Grefachew et al. (2017) Enhancing adoptive cancer immunotherapy with V?2V?2 T cells through pulse zoledronate stimulation. J Immunother Cancer 5:9
Vijay, Rahul; Fehr, Anthony R; Janowski, Ann M et al. (2017) Virus-induced inflammasome activation is suppressed by prostaglandin D2/DP1 signaling. Proc Natl Acad Sci U S A 114:E5444-E5453
Vacaflores, Aldo; Freedman, Samantha N; Chapman, Nicole M et al. (2017) Pretreatment of activated human CD8 T cells with IL-12 leads to enhanced TCR-induced signaling and cytokine production. Mol Immunol 81:1-15
Gullicksrud, Jodi A; Li, Fengyin; Xing, Shaojun et al. (2017) Differential Requirements for Tcf1 Long Isoforms in CD8+ and CD4+ T Cell Responses to Acute Viral Infection. J Immunol 199:911-919

Showing the most recent 10 out of 81 publications