Our laboratory is elucidating the nature of the immune response to tumors and establishing principles which may enhance our ability to immunize patients against known tumor antigens and induce tumor regression with cytokine or cell-transfer therapies. We have developed methodologies for identifying tumor-specific CTL from patients with renal cell cancer and successfully used these techniques to identify unmutated FGF-5 as an HLA-A3 restricted antigen on RCC, recognized by T-cells. This target protein has significant limitations on its clinical utility, such that the discovery of alternative tumor antigens is needed. Continuing these efforts looking at other antigens expressed on RCC, we have found tumor-reactive T-cells in patients with RCC which recognize their own tumors as well as allogeneic RCCs. Many of these cells are CD4 cells, recognizing antigens presented by HLA Class II molecules. The role and efficacy of tumor-reactive CD4+ cells in tumor rejection is still unclear. A more extensive catalog of such antigens will not only clarify our basic understanding of the role of CD4+ cells, but allow the recruitment of this other arm of the cellular immune response against cancer in novel immunotherapies. Renal cancer serves as a particularly useful model, because, unlike melanoma, the preponderance of tumor reactivity seems to reside in the CD4 compartment, yet this cancer is also quite susceptible to immunotherapies which can also treat melanoma (which is dominated by CD8 reactivity). We have developed a system of in vitro lymphocyte stimulation with autologous dendritic cells and autologous tumor which consistently generates tumor-reactive T-cells. We are adapting methods for cloning the antigens recognized to further our understanding of tumor recognition by CD4 cells.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC006660-23
Application #
7594768
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
23
Fiscal Year
2007
Total Cost
$1,252,404
Indirect Cost
Name
National Cancer Institute Division of Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Wang, Qiong J; Yu, Zhiya; Hanada, Ken-Ichi et al. (2017) Preclinical Evaluation of Chimeric Antigen Receptors Targeting CD70-Expressing Cancers. Clin Cancer Res 23:2267-2276
Ilyas, Sadia; Yang, James C (2015) Landscape of Tumor Antigens in T Cell Immunotherapy. J Immunol 195:5117-22
Wang, Qiong J; Hanada, Ken-Ichi; Yang, James C (2008) Characterization of a novel nonclassical T cell clone with broad reactivity against human renal cell carcinomas. J Immunol 181:3769-76
Beck, Kimberly E; Blansfield, Joseph A; Tran, Khoi Q et al. (2006) Enterocolitis in patients with cancer after antibody blockade of cytotoxic T-lymphocyte-associated antigen 4. J Clin Oncol 24:2283-9
Hanada, Ken-Ichi; Yewdell, Jonathan W; Yang, James C (2004) Immune recognition of a human renal cancer antigen through post-translational protein splicing. Nature 427:252-6