This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. This Oklahoma Medical Research Foundation (OMRF) COBRE has a nearly ten year history of successfully identifying and supporting Pilot Projects which lead to additional federal funding and scientific success of our recipients. Indeed, our first five Pilot Projects led to independent, R01 funding of 4 investigators, and all five have vibrant research careers now nearly 9 years later (four in Oklahoma and one leading an Immunology program in Germany). Additional support of Pilot Projects has led to (on average) 4 manuscripts per project, with many high impact papers and invitations to present their work at national/international meetings. In addition, many of our prior COBRE Pilot Projects have led to new collaborations between COBRE investigators within and outside Oklahoma. These interactions have led to collaborative manuscripts in high-impact journals, new scientific directions and transfer of technology across laboratories. A very recent successful collaboration partnered two OMRF COBRE investigators, which led to a co-PI R21 NIAID funded grant. Oklahoma continues to have many outstanding junior investigators with novel project ideas which are ripe for minimal investments with large potential returns. With just one e-mail announcement, we had responses for 17 potential Pilot Projects, twelve from junior COBRE-eligible investigators with ten of these never having received COBRE funds previously. All of these projects proposed to use at least 2 (and many 4) of the proposed scientific cores in this application. Our Pilot Project selection process entails an open competition (with notifications to junior scientists, mentors, section chiefs and program heads), with applications reviewed by our experienced Internal Advisory Committee (collectively with over 100 years of NIH funding) to rank applications. Ranked applications are then reviewed by our External Advisory Committee, and the top projects are funded as resources allow. All applicants (whether or not they receive funding) receive written comments about the application and have a post-review mentoring session with at least one member of the IAC to help improve the applications for future submissions and to suggest alternative funding opportunities. All Pilot Project recipients will present and discuss their progress with an assigned mentoring team, as well as present and discuss results/future directions with the IAC and at the annual EAC review. The Pilot Project Core is also evaluated and improved through a formal evaluation plan outlined in the Administrative Core.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Center Core Grants (P30)
Project #
5P30RR031152-02
Application #
8364937
Study Section
Special Emphasis Panel (ZRR1-RI-2 (01))
Project Start
2011-08-01
Project End
2012-07-31
Budget Start
2011-08-01
Budget End
2012-07-31
Support Year
2
Fiscal Year
2011
Total Cost
$203,962
Indirect Cost
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
077333797
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Waubant, Emmanuelle; Mowry, Ellen M; Krupp, Lauren et al. (2013) Antibody response to common viruses and human leukocyte antigen-DRB1 in pediatric multiple sclerosis. Mult Scler 19:891-5
Koelsch, Kristi A; Webb, Ryan; Jeffries, Matlock et al. (2013) Functional characterization of the MECP2/IRAK1 lupus risk haplotype in human T cells and a human MECP2 transgenic mouse. J Autoimmun 41:168-74
Smith, Kenneth; Muther, Jennifer J; Duke, Angie L et al. (2013) Fully human monoclonal antibodies from antibody secreting cells after vaccination with Pneumovax®23 are serotype specific and facilitate opsonophagocytosis. Immunobiology 218:745-54
Cogman, Abigail R; Chakravarty, Eliza F (2013) The case for Zostavax vaccination in systemic lupus erythematosus. Vaccine 31:3640-3
Ramos, Paula S; Oates, James C; Kamen, Diane L et al. (2013) Variable association of reactive intermediate genes with systemic lupus erythematosus in populations with different African ancestry. J Rheumatol 40:842-9
Sánchez, Elena; Rasmussen, Astrid; Riba, Laura et al. (2012) Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations. Arthritis Rheum 64:3687-94
Gaddy, Jasmine R; Vista, Evan S; Robertson, Julie M et al. (2012) Rheumatic disease among Oklahoma tribal populations: a cross-sectional study. J Rheumatol 39:1934-41
Hughes, Travis; Adler, Adam; Merrill, Joan T et al. (2012) Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus. Ann Rheum Dis 71:694-9
Bruner, Benjamin F; Guthridge, Joel M; Lu, Rufei et al. (2012) Comparison of autoantibody specificities between traditional and bead-based assays in a large, diverse collection of patients with systemic lupus erythematosus and family members. Arthritis Rheum 64:3677-86
Vista, E S; Crowe, S R; Thompson, L F et al. (2012) Influenza vaccination can induce new-onset anticardiolipins but not *2-glycoprotein-I antibodies among patients with systemic lupus erythematosus. Lupus 21:168-74

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