The purpose of the pilot project component of this U19 application is to provide a resource for fundingnew research opportunities that are considered high risk yet with a high potential for making new in-roadsinto the study of human immunology in the context of agents categorized as A-C by NIAID, NIH. Thescientific merit of these applications will be judged primarily as the potential of the projects to produce datawith the highest likelihood to result in RO1 funding. With these objectives in mind, we have selected a groupof senior scientists who have a record of judging grant applications, shown by their history of serving on NIHstudy sections, their ability to obtain NIH funding and their stature in the Immunology community to serve onthe administrative committee in charge of selection of the pilot grants. Each of the individuals who haveagreed to serve are established authorities in the field of Immunology with solid administration experienceand national recognition. They include Drs. Ansari, Jensen, Rich and Stephens. In addition, we are veryfortunate to have the preeminent national bio-defense laboratories of the CDC located within close proximityof Emory University, School of Medicine. More importantly, several of us, including the P.I. of this U19application, Dr. Rafi Ahmed, and Drs. Jensen, Ansari and Stephens have close working relationships withseveral of the components of the CDC, including the Special Pathogens Branch. The working relationshipsare exemplified by joint publications with CDC investigators. With the focus on biodefense for this RFA, wethus have selected 2 investigators (Drs. Damon/poxvirus work and Dr. Quinn/anthrax work) from the CDC tojoin us in the administration of this pilot project component. They will each contribute immensely from theirindividual levels of knowledge and expertise on issues related to biodefense to insure that the pilot projectschosen for funding have this relevant component appropriately included and addressed in the selectedresearch proposals. The proposal outlines the pilot projects administrative committee members, the scope ofthe pilot projects, eligibility and funding guidelines to be utilized, methods we will utilize to seek applicationsfor the pilot projects, the selection criteria we will utilize for funding the projects, milestones that we will useto monitor progress of the pilot projects, an outline for insuring quality of the pilot projects and finally,incentives that we believe are important to provide to individuals who are successful in obtaining RO1funding. Finally, as required, examples of 2 pilot projects that we would consider for funding under thiscomponent of the U19 application are provided. These include studies of the molecular basis for humanregulatory T-cell function (Dr. F. Sallusto) and mechanisms by which small pox virus influences immuneresponses (Dr. Silvestri).

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
3U19AI057266-05S1
Application #
7658466
Study Section
Special Emphasis Panel (ZAI1-PTM-I (M4))
Project Start
2008-04-01
Project End
2009-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
5
Fiscal Year
2008
Total Cost
$189,476
Indirect Cost
Name
Emory University
Department
Type
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Watanabe, Ryu; Maeda, Toshihisa; Zhang, Hui et al. (2018) MMP (Matrix Metalloprotease)-9-Producing Monocytes Enable T Cells to Invade the Vessel Wall and Cause Vasculitis. Circ Res 123:700-715
Weyand, Cornelia M; Shen, Yi; Goronzy, Jorg J (2018) Redox-sensitive signaling in inflammatory T cells and in autoimmune disease. Free Radic Biol Med 125:36-43
Wilson, Patrick C; Cobey, Sarah (2018) Characterization of the immunologic repertoire: A quick start guide. Immunol Rev 284:5-8
Buenrostro, Jason D; Corces, M Ryan; Lareau, Caleb A et al. (2018) Integrated Single-Cell Analysis Maps the Continuous Regulatory Landscape of Human Hematopoietic Differentiation. Cell 173:1535-1548.e16
Stamper, Christopher T; Wilson, Patrick C (2018) What Are the Primary Limitations in B-Cell Affinity Maturation, and How Much Affinity Maturation Can We Drive with Vaccination? Is Affinity Maturation a Self-Defeating Process for Eliciting Broad Protection? Cold Spring Harb Perspect Biol 10:
Mezger, Anja; Klemm, Sandy; Mann, Ishminder et al. (2018) High-throughput chromatin accessibility profiling at single-cell resolution. Nat Commun 9:3647
Ye, Zhongde; Li, Guangjin; Kim, Chulwoo et al. (2018) Regulation of miR-181a expression in T cell aging. Nat Commun 9:3060
Burke, Rachel M; Whitehead Jr, Ralph D; Figueroa, Janet et al. (2018) Effects of Inflammation on Biomarkers of Vitamin A Status among a Cohort of Bolivian Infants. Nutrients 10:
Burke, Rachel M; Rebolledo, Paulina A; Aceituno, Anna M et al. (2018) Effect of infant feeding practices on iron status in a cohort study of Bolivian infants. BMC Pediatr 18:107
Hagan, Thomas; Pulendran, Bali (2018) Will Systems Biology Deliver Its Promise and Contribute to the Development of New or Improved Vaccines? From Data to Understanding through Systems Biology. Cold Spring Harb Perspect Biol 10:

Showing the most recent 10 out of 257 publications