This is a competing application for continued support of an NIAID sponsored multi-disciplinary program for """"""""Research Training in Experimental Immunology"""""""" at the University of Michigan School of Medicine beginning its 20th year. Faculty preceptors with interests in immunology and immunological mechanisms of disease have been selected from the Departments of Pathology, Internal Medicine, Microbiology and Immunology, Pediatrics, Neurology and Surgery. Our senior preceptors direct active, highly regarded laboratories with exemplary records of securing extramural funding. These preceptors have outstanding records in mentoring graduate students and post-doctoral fellows. In addition, we have added some highly regarded new investigators and have established mechanisms to ensure that these new preceptors have ample guidance in becoming accomplished mentors themselves. The program is directed by Dr. Steven Kunkel who has led the program for the last 10 years. Beginning this year, the co-director will be Dr. Bethany Moore who also serves as the Director of the Immunology Graduate Program at the University of Michigan. Drs. Kunkel and Moore will work closely with the T32 advisory committee and the Immunology graduate student affairs committee to advise trainees, monitor curriculum and resolve any issues that arise. The T32 will continue to sponsor several major activities: 1) a weekly seminar for students and post-doctoral fellows to present journal club or works-in progress, 2) a visiting professor monthly seminar where invited guest speakers present their research and spend a day interacting with program faculty and trainees, 3) research colloquium courses which provide in depth training in experimental immunology and special topics relating to translational immunology and 4) a new """"""""i-club"""""""" which will provide additional journal club, career development and networking opportunities for our trainees. In addition, the program provides training in research responsibility and ethics and is committed to continuing to recruit and train talented mentees from underrepresented populations to facilitate the creation of a diverse and talented pool of researchers for the next generation. Support is requested for 6 pre-doctoral and 2 post-doctoral trainees, the same as has been supported previously. This T32 program has been essential to the formation of the Immunology graduate program at the University of Michigan and our success is best measured by the outstanding publication and presentation records of our recent trainees and the excellent post-doctoral and academic positions they earn as they progress.
Immunology is the study of the body's immune system and how it responds in states of health and disease. Many human conditions involve alterations of the normal function of the immune system including cancer, autoimmune diseases, infectious diseases and transplantation. The purpose of this training grant is to train the next generation of scientists in the critical thinking and technical skills necessary to provide mechanistic insight ito how the immune system functions and how to manipulate the immune response to the benefit of human health.
|Kocab, Andrew J; Duckett, Colin S (2016) Inhibitor of apoptosis proteins as intracellular signaling intermediates. FEBS J 283:221-31|
|McCubbrey, Alexandra L; Nelson, Joshua D; Stolberg, Valerie R et al. (2016) MicroRNA-34a Negatively Regulates Efferocytosis by Tissue Macrophages in Part via SIRT1. J Immunol 196:1366-75|
|Xu, Jintao; Eastman, Alison J; Flaczyk, Adam et al. (2016) Disruption of Early Tumor Necrosis Factor Alpha Signaling Prevents Classical Activation of Dendritic Cells in Lung-Associated Lymph Nodes and Development of Protective Immunity against Cryptococcal Infection. MBio 7:|
|Ashley, S L; Wilke, C A; Kim, K K et al. (2016) Periostin regulates fibrocyte function to promote myofibroblast differentiation and lung fibrosis. Mucosal Immunol :|
|Zhou, X; Loomis-King, H; Gurczynski, S J et al. (2016) Bone marrow transplantation alters lung antigen-presenting cells to promote TH17 response and the development of pneumonitis and fibrosis following gammaherpesvirus infection. Mucosal Immunol 9:610-20|
|O'Dwyer, David N; Ashley, Shanna L; Moore, Bethany B (2016) Influences of innate immunity, autophagy, and fibroblast activation in the pathogenesis of lung fibrosis. Am J Physiol Lung Cell Mol Physiol 311:L590-601|
|Baldridge, Megan T; Turula, Holly; Wobus, Christiane E (2016) Norovirus Regulation by Host and Microbe. Trends Mol Med 22:1047-1059|
|Chockley, Peter J; Keshamouni, Venkateshwar G (2016) Immunological Consequences of Epithelial-Mesenchymal Transition in Tumor Progression. J Immunol 197:691-8|
|Ashley, Shanna L; Xia, Meng; Murray, Susan et al. (2016) Six-SOMAmer Index Relating to Immune, Protease and Angiogenic Functions Predicts Progression in IPF. PLoS One 11:e0159878|
|Grifka-Walk, Heather M; Segal, Benjamin M (2016) T-bet promotes the accumulation of encephalitogenic Th17 cells in the CNS. J Neuroimmunol :|
Showing the most recent 10 out of 100 publications