CD47-Targeted Near-Infrared Photoimmunotherapy for Human Bladder Cancer.

Kiss, Bernhard; van den Berg, Nynke S; Ertsey, Robert; McKenna, Kelly; Mach, Kathleen E; Zhang, Chiyuan Amy; Volkmer, Jens-Peter; Weissman, Irving L et al. · Clin Cancer Res · 2019

basic_science · Level V

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Abstract

Near-infrared photoimmunotherapy (NIR-PIT) is a localized molecular cancer therapy combining a photosensitizer-conjugated mAb and light energy. CD47 is an innate immune checkpoint widely expressed on bladder cancer cells, but absent from luminal normal urothelium. Targeting CD47 for NIR-PIT has the potential to selectively induce cancer cell death and minimize damage to normal urothelium. The cytotoxic effect of NIR-PIT with anti-CD47-IR700 was investigated in human bladder cancer cell lines and primary human bladder cancer cells derived from fresh surgical samples. Phagocytosis assays were performed to evaluate macrophage activity after NIR-PIT. Anti-CD47-IR700 was administered to murine xenograft tumor models of human bladder cancer for <i>in vivo</i> molecular imaging and NIR-PIT. Cytotoxicity in cell lines and primary bladder cancer cells significantly increased in a light-dose-dependent manner with CD47-targeted NIR-PIT. Phagocytosis of cancer cells significantly increased with NIR-PIT compared with antibody alone (<i>P</i> = 0.0002). <i>In vivo</i> fluorescence intensity of anti-CD47-IR700 in tumors reached a peak 24-hour postinjection and was detectable for at least 14 days. After a single round of CD47-targeted NIR-PIT, treated animals showed significantly slower tumor growth compared with controls (<i>P</i> < 0.0001). Repeated CD47-targeted NIR-PIT treatment further slowed tumor growth (<i>P</i> = 0.0104) and improved survival compared with controls. CD47-targeted NIR-PIT increased direct cancer cell death and phagocytosis resulting in inhibited tumor growth and improved survival in a murine xenograft model of human bladder cancer.

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