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DOI 10.1016/j.clim.2020.108457

Медицинская библиотека · Clinical immunology (Orlando, Fla.) · 2020

A phase I study of loco-regional immunotherapy by transbronchial injection of α-galactosylceramide-pulsed antigen presenting cells in patients with lung cancer.

Ishibashi Fumihiro, Sakairi Yuichi, Iwata Takekazu, Moriya Yasumitsu, Mizobuchi Teruaki, Hoshino Hidehisa, Yoshida Shigetoshi, Hanaoka Hideki, Yoshino Ichiro, Motohashi Shinichiro

Клиническое исследование I фазыСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

We conducted a phase I study of the trans-bronchial injection of α-galactosylceramide (αGalCer)-pulsed antigen presenting cells (APCs) to evaluate their safety, immune responses, and anti-tumor activities. Patients with advanced or recurrent non-small cell lung cancer (NSCLC) refractory to standard treatments were eligible. αGalCer-pulsed APCs were administered intratumorally or intranodally by bronchoscopy. Twenty-one patients were enrolled in this study. No severe adverse events related to the cell therapy were observed during this study in any patient. After αGalCer-pulsed APCs were administrated, increased iNKT cell numbers were observed in PBMCs from eight cases, and IFN-γ producing cells were increased in the peripheral blood of 10 cases. Regarding clinical responses, one case exhibited a partial response and eight were classified as stable disease. In the tumor microenvironment, IFN-γ expression was upregulated after treatment in partial response or stable disease cases and TGF-β was upregulated in progressive disease cases.

Для цитирования: Ishibashi Fumihiro, Sakairi Yuichi, Iwata Takekazu, Moriya Yasumitsu, Mizobuchi Teruaki, Hoshino Hidehisa, Yoshida Shigetoshi, Hanaoka Hideki, Yoshino Ichiro, Motohashi Shinichiro. A phase I study of loco-regional immunotherapy by transbronchial injection of α-galactosylceramide-pulsed antigen presenting cells in patients with lung cancer.. Clinical immunology (Orlando, Fla.). 2020. DOI: 10.1016/j.clim.2020.108457.

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