The DC generation core facility will consist of two components located at the Baylor Institute for Immunology Research and the Rockefeller University. The cores' primary responsibility will be prepare GMP grade DCs from stage III and stage IV melanoma patients for the clinical trials proposed in projects 1-3. These include DCs derived from CD34+ hematopoietic progenitors [CD34-DC], and monocyte-derived DCs [MDC]. The core will follow standard operating procedures that have been established at each institution for the generation of each type of DC. The cores have successfully generated high quality cells for in vivo studies in healthy volunteers and stage IV melanoma patients. The cores will also provide 2 additional functions: [a] adapt alternative approaches to mature DCs for clinical use, and [b] adapt novel approaches for loading DCs with dying melanoma cells for vaccination purposes. New approaches to mature DCs will be investigated in projects 2 and 3, including the use of poly I:C, TNF alpha and PGE2 vs. standard stimuli e.g. monocyte-conditioned medium. Cross-presentation of antigens from dying cells represent novel approaches to present a broad repertoire of tumor antigens including both CD4 and CD8 epitopes. The core will customize procedures to generate mature GMP grade DCs that have been fed apoptotic cells. In summary the DC core will provide a unique opportunity to optimize and standardize protocols to generate DCs for studies of human tumor immunology and immunotherapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA084512-02
Application #
6500400
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2001-08-01
Project End
2002-07-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Rockefeller University
Department
Type
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Speake, Cate; Presnell, Scott; Domico, Kelly et al. (2015) An interactive web application for the dissemination of human systems immunology data. J Transl Med 13:196
Rongvaux, Anthony; Willinger, Tim; Martinek, Jan et al. (2014) Development and function of human innate immune cells in a humanized mouse model. Nat Biotechnol 32:364-72
Palucka, Karolina; Banchereau, Jacques (2013) Dendritic-cell-based therapeutic cancer vaccines. Immunity 39:38-48
Obermoser, Gerlinde; Presnell, Scott; Domico, Kelly et al. (2013) Systems scale interactive exploration reveals quantitative and qualitative differences in response to influenza and pneumococcal vaccines. Immunity 38:831-44
Palucka, Karolina; Banchereau, Jacques (2013) Human dendritic cell subsets in vaccination. Curr Opin Immunol 25:396-402
Banchereau, Jacques; Thompson-Snipes, LuAnn; Zurawski, Sandra et al. (2012) The differential production of cytokines by human Langerhans cells and dermal CD14(+) DCs controls CTL priming. Blood 119:5742-9
Banchereau, Jacques; Zurawski, Sandra; Thompson-Snipes, LuAnn et al. (2012) Immunoglobulin-like transcript receptors on human dermal CD14+ dendritic cells act as a CD8-antagonist to control cytotoxic T cell priming. Proc Natl Acad Sci U S A 109:18885-90
Palucka, Karolina; Banchereau, Jacques (2012) Cancer immunotherapy via dendritic cells. Nat Rev Cancer 12:265-77
Palucka, Karolina; Ueno, Hideki; Roberts, Lee et al. (2011) Dendritic cell subsets as vectors and targets for improved cancer therapy. Curr Top Microbiol Immunol 344:173-92
McNab, Finlay W; Berry, Matthew P R; Graham, Christine M et al. (2011) Programmed death ligand 1 is over-expressed by neutrophils in the blood of patients with active tuberculosis. Eur J Immunol 41:1941-7

Showing the most recent 10 out of 97 publications