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[癌症的近红外光免疫疗法]

[Near Infrared Photoimmunotherapy for Cancer].

作者信息

Kobayashi Hisataka

机构信息

Molecular Imaging Program, National Cancer Institute(NCI), National Institutes of Health(NIH).

出版信息

Gan To Kagaku Ryoho. 2019 Jan;46(1):28-33.

Abstract

Near infrared photoimmunotherapy(NIR-PIT)is a new molecularly-targeted cancer photo-therapy based on conjugating a near infrared silica-phthalocyanine dye, IRDye700DX(IR700), to a monoclonal antibody(mAb)targeting cell-surface molecules. NIR-PIT targetingEGFR usingthe cetuximab-IR700 conjugate is now in transition to fast-track global Phase Ⅲ clinical trial in late-stage head and neck squamous cell cancer patients. When exposed to NIR light, the conjugate induces a highlyselective necrotic/immunogenic cell death(ICD)only in target-positive, mAb-IR700-bound cancer cells. This cell death occurs as early as 1 minute after exposure to NIR light. Meanwhile, immediately adjacent target-negative cells are unharmed. ICD induced by NIR-PIT promoted maturation of immature dendritic cells(DCs)to maturated DCs that primed cytotoxic Tcells to react with cancer-related antigens released from destroyed cancer cells. Inhibition of immuno-checkpoints including PD-1/PD-L1 axis or CTLA-4 is one of several major methods for enhancingcytotoxicity of tumor-infiltratingT -cells. In this section, I will also discuss NIR-PIT combined with an immuno-checkpoint inhibitor that could treat not only local tumors but also distant untreated metastatic tumors without recurrence in some syngeneic cancer models. Additionally, NIR-PIT to a local tumor combined with local tumor-infiltratingneg ative-regulatory T-cells by CD25-targeted NIR-PIT that is another major methods for enhancingcytotoxicity of tumor-infiltratingT -cells similarly operated in different tumor models. The regimens of NIR-PIT combined with methods for enhancinghost tumor immunity could cure primary and metastatic tumor and yield vaccination effect against treated cancer cells that would be the ultimate form of NIR-PIT in oncology clinic.

摘要

近红外光免疫疗法(NIR-PIT)是一种新型的分子靶向癌症光疗法,它基于将近红外硅酞菁染料IRDye700DX(IR700)与靶向细胞表面分子的单克隆抗体(mAb)相结合。使用西妥昔单抗-IR700偶联物靶向表皮生长因子受体(EGFR)的NIR-PIT目前正处于向晚期头颈鳞状细胞癌患者进行快速全球Ⅲ期临床试验的过渡阶段。当暴露于近红外光时,该偶联物仅在靶阳性、结合了mAb-IR700的癌细胞中诱导高度选择性的坏死/免疫原性细胞死亡(ICD)。这种细胞死亡在暴露于近红外光后1分钟内就会发生。与此同时,紧邻的靶阴性细胞未受损伤。NIR-PIT诱导的ICD促进未成熟树突状细胞(DC)成熟为成熟的DC,后者使细胞毒性T细胞致敏,以与从被破坏的癌细胞中释放的癌症相关抗原发生反应。抑制包括PD-1/PD-L1轴或细胞毒性T淋巴细胞相关抗原4(CTLA-4)在内的免疫检查点是增强肿瘤浸润性T细胞细胞毒性的几种主要方法之一。在本节中,我还将讨论NIR-PIT与免疫检查点抑制剂联合使用的情况,在一些同基因癌症模型中,这种联合使用不仅可以治疗局部肿瘤,还可以治疗远处未治疗的转移性肿瘤且不会复发。此外,对局部肿瘤进行NIR-PIT并通过靶向CD25的NIR-PIT联合局部肿瘤浸润性负调节T细胞,这是增强肿瘤浸润性T细胞细胞毒性的另一种主要方法,在不同的肿瘤模型中也有类似作用。NIR-PIT与增强宿主肿瘤免疫方法联合使用的方案可以治愈原发性和转移性肿瘤,并产生针对已治疗癌细胞的疫苗接种效果,这将是NIR-PIT在肿瘤学临床应用中的最终形式。

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