The administrative core will continue to support ongoing research and help to promote research synergy among members ofthe PPG. The core will continue to provide assistance with grant/manuscript preparation, administrative and tinancial support and establish mechanisms to ensure quality control and efficient usage of PPG resources. Research and administrative meetings will be scheduled at regular intervals to discuss progress and problems. The core will organize meetings of the internal advisory committee to insure appropriate oversight ofthe program. In addition, the core will organize and provide logistical support for an annual meeting with the external advisory committee and will organize the biodefense seminar series supported by this grant. This core will also provide statistical support for experimental design and data analysis for each ofthe projects. Day-to-day administrative support for grants management, purchase requisitions, animal care compliance, safety compliance, manuscript and reporting activities will also be provided to PPG members. Overall, the administrative core will continue to provide essential support services in orderto help foster the ongoing success ofthe Program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI056172-09
Application #
8728382
Study Section
Special Emphasis Panel (ZAI1-PA-I)
Project Start
Project End
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
9
Fiscal Year
2014
Total Cost
$131,526
Indirect Cost
$38,279
Name
University of Connecticut
Department
Type
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030
Tsurutani, Naomi; Mittal, Payal; St Rose, Marie-Clare et al. (2016) Costimulation Endows Immunotherapeutic CD8 T Cells with IL-36 Responsiveness during Aerobic Glycolysis. J Immunol 196:124-34
Song, Jeongmin; Wilhelm, Cara L; Wangdi, Tamding et al. (2016) Absence of TLR11 in Mice Does Not Confer Susceptibility to Salmonella Typhi. Cell 164:827-8
Benoun, Joseph M; Labuda, Jasmine C; McSorley, Stephen J (2016) Collateral Damage: Detrimental Effect of Antibiotics on the Development of Protective Immune Memory. MBio 7:
Svedova, Julia; Tsurutani, Naomi; Liu, Wenhai et al. (2016) TNF and CD28 Signaling Play Unique but Complementary Roles in the Systemic Recruitment of Innate Immune Cells after Staphylococcus aureus Enterotoxin A Inhalation. J Immunol 196:4510-21
Romagnoli, Pablo A; Sheridan, Brian S; Pham, Quynh-Mai et al. (2016) IL-17A-producing resident memory γδ T cells orchestrate the innate immune response to secondary oral Listeria monocytogenes infection. Proc Natl Acad Sci U S A 113:8502-7
Cauley, Linda S (2016) Environmental cues orchestrate regional immune surveillance and protection by pulmonary CTLs. J Leukoc Biol 100:905-912
Romagnoli, P A; Fu, H H; Qiu, Z et al. (2016) Differentiation of distinct long-lived memory CD4 T cells in intestinal tissues after oral Listeria monocytogenes infection. Mucosal Immunol :
Cauley, Linda S; Vella, Anthony T (2015) Why is coinfection with influenza virus and bacteria so difficult to control? Discov Med 19:33-40
Colpitts, Sara L; Puddington, Lynn; Lefrançois, Leo (2015) IL-15 receptor α signaling constrains the development of IL-17-producing γδ T cells. Proc Natl Acad Sci U S A 112:9692-7
Pham, Oanh H; McSorley, Stephen J (2015) Protective host immune responses to Salmonella infection. Future Microbiol 10:101-10

Showing the most recent 10 out of 76 publications