The Administrative Core will oversee the entire MGH/Harvard AADCRC program, manage the day-to-day Center activities and direct the multi-disciplinary collaborative research activities. This Core will be responsible for administering the overall budgets of the Projects and Cores, finalizing contractual arrangements and ensuring that the aims of each project are being met. The Administrative Core will also be responsible for ensuring the Human Subjects Core, the Tetramer Core, and Bioinformatics Core are used fairly. The Administrative Core will be directly involved with managing, coordinating and overseeing the administrative functions related to the complex protocol process and safety procedures for the projects and cores. The Administrative Core will facilitate collaboration between the projects and cores by organizing mandatory monthly meetings for all personnel associated with the Center. The Administrative Core will also coordinate and support the invitation of two outside speakers per year whose research is directly related to the Center. The Core will effectively and regularly communicate with all PI/PD's, project and core staff, and administrators.

Agency
National Institute of Health (NIH)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI095261-04
Application #
8707952
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Cho, Josalyn L; Ling, Morris F; Adams, David C et al. (2016) Allergic asthma is distinguished by sensitivity of allergen-specific CD4+ T cells and airway structural cells to type 2 inflammation. Sci Transl Med 8:359ra132
Urso, Katia; Alvarez, David; Cremasco, Viviana et al. (2016) IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease. JCI Insight 1:
Hondowicz, Brian D; An, Dowon; Schenkel, Jason M et al. (2016) Interleukin-2-Dependent Allergen-Specific Tissue-Resident Memory Cells Drive Asthma. Immunity 44:155-66
Proekt, Irina; Miller, Corey N; Jeanne, Marion et al. (2016) LYN- and AIRE-mediated tolerance checkpoint defects synergize to trigger organ-specific autoimmunity. J Clin Invest 126:3758-3771
Jhunjhunwala, Siddharth; Alvarez, David; Aresta-DaSilva, Stephanie et al. (2016) Frontline Science: Splenic progenitors aid in maintaining high neutrophil numbers at sites of sterile chronic inflammation. J Leukoc Biol 100:253-60
Ling, Morris F; Luster, Andrew D (2016) Allergen-Specific CD4(+) T Cells in Human Asthma. Ann Am Thorac Soc 13 Suppl 1:S25-30
Leung, John; Mehrzad, Raman; Hundal, Navneet Virk et al. (2015) Longitudinal Perspective on Managing Refractory Eosinophilic Esophagitis. J Allergy Clin Immunol Pract 3:951-6
Patil, Sarita U; Ogunniyi, Adebola O; Calatroni, Agustin et al. (2015) Peanut oral immunotherapy transiently expands circulating Ara h 2-specific B cells with a homologous repertoire in unrelated subjects. J Allergy Clin Immunol 136:125-134.e12
Shade, Kai-Ting C; Platzer, Barbara; Washburn, Nathaniel et al. (2015) A single glycan on IgE is indispensable for initiation of anaphylaxis. J Exp Med 212:457-67
Mattapallil, Mary J; Silver, Phyllis B; Cortes, Lizette M et al. (2015) Characterization of a New Epitope of IRBP That Induces Moderate to Severe Uveoretinitis in Mice With H-2b Haplotype. Invest Ophthalmol Vis Sci 56:5439-49

Showing the most recent 10 out of 43 publications