Center for Translational Cancer Research, Institute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Nat Nanotechnol. 2021 Dec;16(12):1424-1434. doi: 10.1038/s41565-021-00982-5. Epub 2021 Oct 25.
Chimeric antigen receptor (CAR) T cell-based immunotherapy, approved by the US Food and Drug Administration, has shown curative potential in patients with haematological malignancies. However, owing to the lack of control over the location and duration of the anti-tumour immune response, CAR T cell therapy still faces safety challenges arising from cytokine release syndrome and on-target, off-tumour toxicity. Herein, we present the design of light-switchable CAR (designated LiCAR) T cells that allow real-time phototunable activation of therapeutic T cells to precisely induce tumour cell killing. When coupled with imaging-guided, surgically removable upconversion nanoplates that have enhanced near-infrared-to-blue upconversion luminescence as miniature deep-tissue photon transducers, LiCAR T cells enable both spatial and temporal control over T cell-mediated anti-tumour therapeutic activity in vivo with greatly mitigated side effects. Our nano-optogenetic immunomodulation platform not only provides a unique approach to interrogate CAR-mediated anti-tumour immunity, but also sets the stage for developing precision medicine to deliver personalized anticancer therapy.
嵌合抗原受体 (CAR) T 细胞免疫疗法已获美国食品和药物管理局批准,在血液系统恶性肿瘤患者中显示出治疗潜力。然而,由于缺乏对肿瘤免疫反应位置和持续时间的控制,CAR T 细胞疗法仍然面临细胞因子释放综合征和靶向肿瘤毒性的安全挑战。在此,我们设计了光控型 CAR(LiCAR)T 细胞,可实时光控激活治疗性 T 细胞,从而精确诱导肿瘤细胞杀伤。当与成像引导的、可手术去除的上转换纳米板结合使用时,这些纳米板具有增强的近红外到蓝光上转换发光,作为微型深部组织光子传感器,LiCAR T 细胞能够在体内对 T 细胞介导的抗肿瘤治疗活性进行时空控制,同时大大减轻副作用。我们的纳米光遗传学免疫调节平台不仅为研究 CAR 介导的抗肿瘤免疫提供了一种独特的方法,也为开发精准医学以提供个性化抗癌疗法奠定了基础。