T cell activation upon exposure to patient-derived tumor tissue: A functional assay to select patients for adoptive T cell therapy
July 2010
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Gene-engineered T cell therapy represents a promising strategy to treat cancers. To enable pre-selection of patients sensitive to this type of treatment we have setup and validated a T cell activation assay to test antigen expression on patient-derived tumor tissues. Chimeric antibody-based receptor (CAR) directed against CAIX, currently used in a clinical trial to treat RCC patients, was used as a model receptor. Primary human T cells expressing CAIX CAR were able to respond to CAIX-positive but not CAIX-negative tumor tissue and showed an increased production of IFNγ, TNFα, IL-10 and IL-4, but not IL-2 or IL-5. Tumor tissue driven responses of primary T cells were paralleled by NFAT activation measured in CAR-transduced Jurkat T cells, which was shown to be triggered in a CAR and antigen-specific manner. Next, the reporter gene assay was applied to two independent PSMA CARs, which both mediated NFAT activation in response to tumor tissue. Taken together, a sensitive and donor-independent assay was established to measure T cell activation upon exposure to patient-derived tumor tissue, which may facilitate pre-selection of patients for clinical adoptive T cell therapy.
- article
- human
- signal transduction
- priority journal
- controlled study
- clinical trial
- human cell
- T lymphocyte activation
- T lymphocyte
- antigen
- gene therapy
- unclassified drug
- Prostate cancer
- human tissue
- tumor necrosis factor alpha
- interleukin 2
- adoptive transfer
- cytokine production
- patient selection
- gamma interferon
- interleukin 10
- immunohistochemistry
- histopathology
- antigen specificity
- antigen expression
- interleukin 4
- interleukin 5
- leukemia cell line
- kidney carcinoma
- Chimeric antibody-based receptor (CAR)
- Gene-modified T cells
- NFAT reporter gene assay
- T cell therapy
- adoptive T lymphocyte therapy
- cancer tissue
- carbonate dehydratase IX
- cell assay
- cell therapy
- chimeric antibody based receptor
- chimeric antibody
- prostate specific membrane antigen
- reporter gene
- transcription factor NFAT