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Updated: Jun 4, 2025

Near Infrared Photoimmunotherapy for Mouse Models of Pleural Dissemination
Published on: February 9, 2021
Tissue factor targeted near-infrared photoimmunotherapy: a versatile therapeutic approach for malignancies
Seiichiro Takao1, Hiroshi Fukushima1, Aki Furusawa1
1Molecular Imaging Branch, Center for Cancer Research, National Cancer Institute, NIH, 10 Center Drive, Bethesda, MD, 20892, USA.
Abstract:
Tissue factor (TF) is a cell surface protein that plays a role in blood clotting but is also commonly expressed in many cancers. Recent research implicated TF in cancer proliferation, metastasis, angiogenesis, and immune escape. Therefore, TF can be considered a viable therapeutic target against cancer. Herein, we developed and tested a TF-targeted near-infrared photoimmunotherapy (NIR-PIT) as a potential treatment for several types of cancer. Tisotumab, a TF antibody, was conjugated to IR700. The efficacy of TF-targeted NIR-PIT was investigated using multiple cancer cell lines (A431; epidermoid carcinoma, HPAF-II; pancreatic adenocarcinoma, HSC-2; oral carcinoma, HT1376-luc; bladder carcinoma, MDAMB231; breast adenocarcinoma, and SKOV3-luc; ovarian serous cystadenocarcinoma) in vitro. In vivo, the efficacy of TF-targeted NIR-PIT was evaluated in HPAF-II and A431 xenograft mouse models. Pathologic changes in these tumors after NIR-PIT were evaluated in these tumor models. All cancer lines demonstrated TF expression in vitro and in vivo. Additionally, TF expression was documented to localize to cancer cells in tumors. In vitro, TF-targeted NIR-PIT caused cell death in a light dose-dependent manner. In vivo, TF-targeted NIR-PIT suppressed tumor growth and improved survival rates compared to controls. Furthermore, in vivo NIR-PIT showed histological signs of cancer cell damage, such as cytoplasmic vacuolation, nuclear dysmorphism, and extracellular leakage of LDHA consistent with cell death. In conclusion, TF-targeted NIR-PIT holds promise as a treatment for multiple cancer models expressing TF, spanning multiple cancer types.
Insights
This study shows that tissue factor (TF)-targeted near-infrared photoimmunotherapy (NIR-PIT) effectively kills various cancer cells. This novel cancer treatment suppressed tumor growth and improved survival in mouse models.
Area of Science:
- Oncology
- Immunotherapy
- Biomedical Engineering
Background:
- Tissue factor (TF) is a protein involved in blood clotting and cancer progression.
- TF is expressed in various cancer types, making it a potential therapeutic target.
- Near-infrared photoimmunotherapy (NIR-PIT) is an emerging cancer treatment modality.
Purpose of the Study:
- To develop and evaluate a TF-targeted NIR-PIT for treating multiple cancer types.
- To assess the efficacy of TF-targeted NIR-PIT both in vitro and in vivo.
- To investigate the underlying mechanisms of cell death induced by TF-targeted NIR-PIT.
Main Methods:
- Conjugation of Tisotumab (a TF antibody) with IR700 dye.
- In vitro testing on multiple cancer cell lines (A431, HPAF-II, HSC-2, HT1376-luc, MDAMB231, SKOV3-luc).
- In vivo evaluation using HPAF-II and A431 xenograft mouse models.
Main Results:
- All tested cancer cell lines demonstrated TF expression.
- TF-targeted NIR-PIT induced dose-dependent cancer cell death in vitro.
- In vivo studies showed suppressed tumor growth, improved survival rates, and histological evidence of cancer cell damage.
Conclusions:
- TF-targeted NIR-PIT is a promising therapeutic strategy for TF-expressing cancers.
- This approach shows potential across multiple cancer types.
- Further research into TF-targeted NIR-PIT is warranted for clinical application.
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