Cancer Immunotherapeutics Program ABSTRACT The mission of the Cancer Immunotherapeutics (CI) Program is to develop novel immunotherapy interventions that harness patients? immune responses for more specific and less toxic cancer therapies, and translate them into clinical practice. To achieve this goal, the Program has three themes: 1) Develop approaches to enhance efficacy of adoptive T cell therapy and cancer vaccines; 2) Modulate the tumor microenvironment to enhance immunotherapy; and 3) Develop novel antibody therapies and imaging modalities. Within each of these themes, research is ongoing to reduce health disparities within our catchment area. Led by Peter Lee, MD and Hua Yu, PhD, the CI Program spans basic, translational, and clinical research. To translate discoveries into therapies, the CI Program receives support from the City of Hope Comprehensive Cancer Center (COHCCC) through the GMP Manufacturing Core, consisting of three cGMP manufacturing facilities that can produce clinical grade antibody-based therapeutics and small molecule drugs. Targeted recruits with national prominence have added both depth and breadth to the program and include Drs. Mingye Feng, Edwin Manuel, Kim Margolin, Laleh Melstrom, Javier Ogembo, Susanne Warner, Yanghee Woo, and Weiping Zou. The major areas of research focus in the CI Program are strengthened by extensive collaborations with other investigators at COHCCC as well as collaborations with investigators at other academic institutions and industry. Sponsored activities include monthly research meetings, monthly seminars, an annual retreat, and annual pilot funding. Membership: 21 Program Members representing 7 basic and clinical departments Publications: 176 total. 18.2% intra-programmatic; 64.8% inter-programmatic; 35.8% inter-institutional Funding: $4,177,832 peer-reviewed; $2,134,027 of which is NCI funding

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA033572-38
Application #
10059208
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Roberson, Sonya
Project Start
1997-08-01
Project End
2022-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
38
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Beckman Research Institute/City of Hope
Department
Type
DUNS #
027176833
City
Duarte
State
CA
Country
United States
Zip Code
91010
Mendez-Dorantes, Carlos; Bhargava, Ragini; Stark, Jeremy M (2018) Repeat-mediated deletions can be induced by a chromosomal break far from a repeat, but multiple pathways suppress such rearrangements. Genes Dev 32:524-536
Bzymek, Krzysztof P; Puckett, James W; Zer, Cindy et al. (2018) Mechanically interlocked functionalization of monoclonal antibodies. Nat Commun 9:1580
Nguyen, Huong Q; Ruel, Nora; Macias, Mayra et al. (2018) Translation and Evaluation of a Lung Cancer, Palliative Care Intervention for Community Practice. J Pain Symptom Manage 56:709-718
Satheesan, Sangeetha; Li, Haitang; Burnett, John C et al. (2018) HIV Replication and Latency in a Humanized NSG Mouse Model during Suppressive Oral Combinational Antiretroviral Therapy. J Virol 92:
Zhang, Jing; He, Zhiheng; Sen, Subha et al. (2018) TCF-1 Inhibits IL-17 Gene Expression To Restrain Th17 Immunity in a Stage-Specific Manner. J Immunol 200:3397-3406
Sun, Jie; He, Xin; Zhu, Yinghui et al. (2018) SIRT1 Activation Disrupts Maintenance of Myelodysplastic Syndrome Stem and Progenitor Cells by Restoring TET2 Function. Cell Stem Cell 23:355-369.e9
Miao, Yifei; Ajami, Nassim E; Huang, Tse-Shun et al. (2018) Enhancer-associated long non-coding RNA LEENE regulates endothelial nitric oxide synthase and endothelial function. Nat Commun 9:292
Sen, Subha; Wang, Fei; Zhang, Jing et al. (2018) SRC1 promotes Th17 differentiation by overriding Foxp3 suppression to stimulate ROR?t activity in a PKC-?-dependent manner. Proc Natl Acad Sci U S A 115:E458-E467
Murad, John P; Kozlowska, Anna K; Lee, Hee Jun et al. (2018) Effective Targeting of TAG72+ Peritoneal Ovarian Tumors via Regional Delivery of CAR-Engineered T Cells. Front Immunol 9:2268
Brown, Christine E; Aguilar, Brenda; Starr, Renate et al. (2018) Optimization of IL13R?2-Targeted Chimeric Antigen Receptor T Cells for Improved Anti-tumor Efficacy against Glioblastoma. Mol Ther 26:31-44

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