PD-L1 near Infrared Photoimmunotherapy of Ovarian Cancer Model.
Jiefu JinIshwarya SivakumarYelena MironchikBalaji KrishnamacharyFlonné WildesJames D BarnettChien-Fu HungSridhar NimmagaddaHisataka KobayashiZaver M BhujwallaMarie-France PenetPublished in: Cancers (2022)
(1) Background: Despite advances in surgical approaches and drug development, ovarian cancer is still a leading cause of death from gynecological malignancies. Patients diagnosed with late-stage disease are treated with aggressive surgical resection and chemotherapy, but recurrence with resistant disease is often observed following treatment. There is a critical need for effective therapy for late-stage ovarian cancer. Photoimmunotherapy (PIT), using an antibody conjugated to a near infrared (NIR) dye, constitutes an effective theranostic strategy to detect and selectively eliminate targeted cell populations. (2) Methods: Here, we are targeting program death ligand 1 (PD-L1) using NIR-PIT in a syngeneic mouse model of ovarian cancer. PD-L1 PIT-mediated cytotoxicity was quantified in RAW264.7 macrophages and ID8-Defb29-VEGF cells in culture, and in vivo with orthotopic ID8-Defb29-VEGF tumors. (3) Results: Treatment efficacy was observed both in vitro and in vivo. (4) Conclusions: Our data highlight the need for further investigations to assess the potential of using NIR-PIT for ovarian cancer therapy to improve the treatment outcome of ovarian cancer.
Keyphrases
- cancer therapy
- photodynamic therapy
- fluorescence imaging
- end stage renal disease
- newly diagnosed
- endothelial cells
- chronic kidney disease
- drug release
- ejection fraction
- fluorescent probe
- squamous cell carcinoma
- single cell
- oxidative stress
- prognostic factors
- stem cells
- risk assessment
- signaling pathway
- locally advanced
- cell proliferation
- cell death
- mesenchymal stem cells
- peritoneal dialysis
- patient reported outcomes
- rectal cancer
- genetic diversity