Related Experiment Video
Updated: Feb 17, 2026
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer
Gemma L Owens1,2, Victoria E Sheard1, Milena Kalaitsidou1
1Clinical and Experimental Immunotherapy Group.
Abstract:
Chimeric antigen receptor (CAR) T cells represent a novel targeted approach to overcome both quantitative and qualitative shortfalls of the host immune system relating to the detection and subsequent destruction of tumors. The identification of antigens expressed specifically on the surface of tumor cells is a critical first step in the ability to utilize CAR T cells for the treatment of cancer. The 5T4 is a tumor-associated antigen which is expressed on the cell surface of most solid tumors including ovarian cancer. Matched blood and tumor samples were collected from 12 patients with ovarian cancer; all tumors were positive for 5T4 expression by immunohistochemistry. Patient T cells were effectively transduced with 2 different anti-5T4 CAR constructs which differed in their affinity for the target antigen. Co-culture of CAR T cells with matched autologous tumor disaggregates resulted in antigen-specific secretion of IFN-gamma. Furthermore, assessment of the efficacy of anti-5T4 CAR T cells in a mouse model resulted in therapeutic benefit against established ovarian tumors. These results demonstrate proof of principle that 5T4 is an attractive target for immune intervention in ovarian cancer and that patient T cells engineered to express a 5T4-specific CAR can recognize and respond physiologically to autologous tumor cells.
Insights
Chimeric antigen receptor (CAR) T-cell therapy shows promise for ovarian cancer. Engineered T cells targeting the 5T4 antigen demonstrated tumor recognition and therapeutic benefit in preclinical models.
Area of Science:
- Immunology
- Oncology
- Biotechnology
Background:
- Chimeric antigen receptor (CAR) T cells offer a targeted immunotherapy approach against cancers.
- The 5T4 antigen is a tumor-associated antigen present on most solid tumors, including ovarian cancer.
Purpose of the Study:
- To evaluate the potential of 5T4-specific CAR T cells for ovarian cancer treatment.
- To assess the efficacy of anti-5T4 CAR T cells in preclinical models.
Main Methods:
- Collected matched blood and tumor samples from 12 ovarian cancer patients.
- Engineered patient T cells with two distinct anti-5T4 CAR constructs.
- Co-cultured CAR T cells with autologous tumor cells and evaluated responses in a mouse model.
Main Results:
- All patient tumors expressed the 5T4 antigen.
- Engineered T cells showed antigen-specific IFN-gamma secretion upon co-culture with autologous tumors.
- Anti-5T4 CAR T cells provided therapeutic benefit against established ovarian tumors in vivo.
Conclusions:
- 5T4 is a viable target for immune intervention in ovarian cancer.
- Patient-derived T cells engineered with anti-5T4 CARs can recognize and respond to autologous tumor cells.
- This study provides proof of principle for 5T4-targeted CAR T-cell therapy in ovarian cancer.

