The Administrative Core will be responsible for providing scientific administration and coordination, fiscal oversight and administrative support for this PPG. The Administrative Core will coordinate PPG scientific group meetings among investigators at Harvard Medical School, and Massachusetts General Hospital. The Administrative Core will also design, implement and maintain a PPG website to facilitate effective communications among internal and external collaborators and the public. In addition, the Administrative Core will arrange an annual PPG meeting for investigators and the members of the Internal and External Adivisory Committees in Boston. Administratively, this Core will coordinate annual progress reports and renewal of sub-contract agreements, and will liaison between the grants offices of the various institutions and the Harvard Medical School Sponsored Programs Administration office. Ulrich H. von Andrian and Harvard Medical School, are responsible for this application and for the collaborative research activities described.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI112521-01
Application #
8742511
Study Section
Special Emphasis Panel (ZAI1-BDP-I (M1))
Project Start
Project End
Budget Start
2014-08-15
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
Total Cost
$71,489
Indirect Cost
$20,347
Name
Harvard Medical School
Department
Type
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Stelekati, Erietta; Chen, Zeyu; Manne, Sasikanth et al. (2018) Long-Term Persistence of Exhausted CD8 T Cells in Chronic Infection Is Regulated by MicroRNA-155. Cell Rep 23:2142-2156
Garcia-Castillo, Maria Daniela; Chinnapen, Daniel J-F; Te Welscher, Yvonne M et al. (2018) Mucosal absorption of therapeutic peptides by harnessing the endogenous sorting of glycosphingolipids. Elife 7:
Carty, Shannon A; Gohil, Mercy; Banks, Lauren B et al. (2018) The Loss of TET2 Promotes CD8+ T Cell Memory Differentiation. J Immunol 200:82-91
Dougan, Michael; Ingram, Jessica R; Jeong, Hee-Jin et al. (2018) Targeting Cytokine Therapy to the Pancreatic Tumor Microenvironment Using PD-L1-Specific VHHs. Cancer Immunol Res 6:389-401
Bengsch, Bertram; Ohtani, Takuya; Khan, Omar et al. (2018) Epigenomic-Guided Mass Cytometry Profiling Reveals Disease-Specific Features of Exhausted CD8 T Cells. Immunity 48:1029-1045.e5
Henrickson, Sarah E; Manne, Sasikanth; Dolfi, Douglas V et al. (2018) Genomic Circuitry Underlying Immunological Response to Pediatric Acute Respiratory Infection. Cell Rep 22:411-426
Vella, Laura A; Herati, Ramin S; Wherry, E John (2017) CD4+ T Cell Differentiation in Chronic Viral Infections: The Tfh Perspective. Trends Mol Med 23:1072-1087
Tomov, Vesselin T; Palko, Olesya; Lau, Chi Wai et al. (2017) Differentiation and Protective Capacity of Virus-Specific CD8+ T Cells Suggest Murine Norovirus Persistence in an Immune-Privileged Enteric Niche. Immunity 47:723-738.e5
Herati, Ramin Sedaghat; Muselman, Alexander; Vella, Laura et al. (2017) Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells. Sci Immunol 2:
Deruaz, Maud; Murooka, Thomas T; Ji, Sophina et al. (2017) Chemoattractant-mediated leukocyte trafficking enables HIV dissemination from the genital mucosa. JCI Insight 2:e88533

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