The Immunomonitoring Core consists of two components located at the Baylor Institute for? Immunology Research (BUR) and the Rockefeller University (RU). The primary objectives of? Immunomonitoring Core are: 1) To carry out, in a standardized way, several assays of immune function in? patients enrolled in the clinical studies proposed in this Program Project. The assays performed by the Core? will be prioritized. Blood samples from RU will be shipped to Dallas. 2) To prepare peptide mixtures from? defined tumor antigens to monitor immune responses in HLA-A201 negative patients vaccinated with? autologous DCs loaded with killed tumor cells, either allogeneic melanoma cells or autologous myeloma? cells. The use of peptide mixtures will also enable the analysis of CD4 T cell responses and spreading of the? immune response to other epitopes and/or antigens. Peptide mixtures will be prepared at RU where they are? already being used to monitor HIV specific immunity. Vaccine induced immune responses will be measured? from a) fresh blood (memory effectors) with tetramers and cytokine ELISPOT (IFN gamma), and b) recall? cultures (recall memory cells) with tetramers, cytokine ELISPOT and assays to assess cytolytic activity? against tumor cells (either allogeneic melanoma cells lines or autologous myeloma cells). 3) To use EPIMAX? assay to measure the immune function, a combined proliferation/cytokine assay with peptide mixtures. This? Core will establish the magnitude and breadth of tumor-specific immunity induced using different types of DC? vaccines, different preparations of tumor antigens loaded onto DC vaccines, and different adjunct therapies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA084512-06
Application #
7460929
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
6
Fiscal Year
2007
Total Cost
$114,481
Indirect Cost
Name
Baylor Research Institute
Department
Type
DUNS #
145745022
City
Dallas
State
TX
Country
United States
Zip Code
75204
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) Human dendritic cell subsets in vaccination. Curr Opin Immunol 25:396-402
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
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