This proposal seeks continuation of a successful training program in systemic autoimmunity at the Beth Israel Medical Deaconess Medical Center (BIDMC), Harvard Medical School (HMS). It requests support for three trainees each year to spend at least two years in the program. Trainees enter the program through one of the following tracks: Physicians who seek training in rheumatology or nephrology, physicians who enter other clinical fellowship programs including neurology and dermatology, physicians who have completed clinical training in a field relevant to systemic autoimmune diseases and PhDs with background in immunology, biochemistry and cell/molecular biology. The major criterion for selection is evidence of commitment to the study of systemic autoimmune diseases. Through this training physicians will develop skills in immunology and biology/biochemistry, whereas PhDs will become familiar with clinical issues pertinent to the study of systemic autoimmune diseases. Research activities will span studies in human and animal T cells, B cells, NKT cells, macrophages, mast cells, costimulation, immune cell signaling, immune tolerance, control of cytokine expression and function, pertinent aspects of regional immunology and biology (kidney, skin and nervous system), human genetics, immunodeficiency, complement and immunomodulation. The chief method of instruction involves personal involvement in a program of basic research under the close supervision of a faculty member. Moreover, a structured program of didactic courses in research seminars, journal clubs, research presentations in national and international meetings and grant writing is in place. The primary facilities for training are at BIDMC and HMS-affiliated institutions. The Program will be administered by the Program Director assisted by two senior experienced mentors, an administrator and three committees (Faculty, Internal and External Advisory) and evaluated through a rigorous process. Graduating trainees will be able to plan, seek funding and execute cutting edge research in systemic autoimmune diseases and will be properly tooled to develop new diagnostics and therapeutics.

Public Health Relevance

This program develops top-notch researchers in the study of Systemic Autoimmune Diseases who will lead basic and Clinical research in academic centers to advance the care of people suffering from these diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI074549-07
Application #
8906722
Study Section
Allergy, Immunology, and Transplantation Research Committee (AITC)
Program Officer
Gondre-Lewis, Timothy A
Project Start
2008-08-01
Project End
2019-07-31
Budget Start
2015-08-01
Budget End
2016-07-31
Support Year
7
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
Suárez-Fueyo, Abel; Bradley, Sean J; Katsuyama, Takayuki et al. (2018) Downregulation of CD3? in NK Cells from Systemic Lupus Erythematosus Patients Confers a Proinflammatory Phenotype. J Immunol 200:3077-3086
Saggu, Gurpanna; Okubo, Koshu; Chen, Yunfeng et al. (2018) Cis interaction between sialylated Fc?RIIA and the ?I-domain of Mac-1 limits antibody-mediated neutrophil recruitment. Nat Commun 9:5058
Crispin, Jose C; Hedrich, Christian M; Suárez-Fueyo, Abel et al. (2017) SLE-Associated Defects Promote Altered T Cell Function. Crit Rev Immunol 37:39-58
Kasper, Isaac R; Apostolidis, Sokratis A; Sharabi, Amir et al. (2016) Empowering Regulatory T Cells in Autoimmunity. Trends Mol Med 22:784-797
Sekar, Aswin; Bialas, Allison R; de Rivera, Heather et al. (2016) Schizophrenia risk from complex variation of complement component 4. Nature 530:177-83
Suárez-Fueyo, Abel; Bradley, Sean J; Tsokos, George C (2016) T cells in Systemic Lupus Erythematosus. Curr Opin Immunol 43:32-38
Macosko, Evan Z; Basu, Anindita; Satija, Rahul et al. (2015) Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets. Cell 161:1202-1214
Bradley, Sean J; Suarez-Fueyo, Abel; Moss, David R et al. (2015) T Cell Transcriptomes Describe Patient Subtypes in Systemic Lupus Erythematosus. PLoS One 10:e0141171
Bove, Riley; Secor, Elizabeth; Chibnik, Lori B et al. (2014) Age at surgical menopause influences cognitive decline and Alzheimer pathology in older women. Neurology 82:222-9
Bove, Riley; Musallam, Alexander; Healy, Brian C et al. (2013) No sex-specific difference in disease trajectory in multiple sclerosis patients before and after age 50. BMC Neurol 13:73

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