Near-infrared photoimmunotherapy and anti-cancer immunity.
Kohei NakajimaMikako OgawaPublished in: International immunology (2023)
The activation of the anti-cancer immune system is an important strategy to control cancer. A new form of cancer phototherapy, near-infrared photoimmunotherapy (NIR-PIT), was approved for clinical use in 2020 and uses IRDye® 700DX (IR700)-conjugated antibodies and NIR light. After irradiation with NIR light, the antibody-IR700 conjugate forms water-insoluble aggregations on the plasma membrane of target cells. This aggregation causes lethal damage to the plasma membrane, and effectively leads to immunogenic cell death (ICD). Subsequently, ICD activates anti-cancer immune cells such as dendritic cells and cytotoxic T cells. Combination therapy with immune-checkpoint blockade has synergistically improved the anti-cancer effects of NIR-PIT. Additionally, NIR-PIT can eliminate immunosuppressive immune cells in light-irradiated tumors by using specific antibodies against regulatory T cells and myeloid-derived suppressor cells. In addition to cancer-cell-targeted NIR-PIT, such immune-cell-targeted NIR-PIT has shown promising results by activating the anti-cancer immune system. Furthermore, NIR-PIT can be used to manipulate the tumor microenvironment by eliminating only targeted cells in the tumor, and thus it also can be used to gain insight into immunity in basic research.
Keyphrases
- photodynamic therapy
- drug release
- fluorescence imaging
- fluorescent probe
- induced apoptosis
- cell cycle arrest
- regulatory t cells
- dendritic cells
- cell death
- combination therapy
- cancer therapy
- signaling pathway
- papillary thyroid
- oxidative stress
- endoplasmic reticulum stress
- squamous cell carcinoma
- immune response
- cell proliferation
- radiation therapy
- pi k akt
- childhood cancer