抗gd2抗体近红外光免疫治疗神经母细胞瘤和骨肉瘤

Jimei Zhao , Kohei Nakajima , Masahiro Ueki , Yukayo Terashita , Shinsuke Hirabayashi , Yuko Cho , Mikako Ogawa , Atsushi Manabe
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引用次数: 0

摘要

近红外光免疫疗法(NIR-PIT)是一种特异性靶向癌细胞的新型癌症治疗方法。在NIR-PIT中,针对癌症抗原的抗体-光吸收偶联物(APCs)靶向癌细胞。与抗原结合的apc在nir光照射下杀死目标细胞。NIR-PIT已在日本临床应用于头颈部鳞状细胞癌,但未应用于儿科癌症。一般来说,神经母细胞瘤和骨肉瘤表达双神经节苷脂(GD2),这使得靶向GD2的NIR-PIT成为一种额外的治疗选择。方法将人GD2单克隆抗体(克隆3F8)与光吸收剂IRDyeⓇ700DX (IR700)偶联。体外和体内实验采用人神经母细胞瘤细胞(SK-N-SH),体外实验采用人骨肉瘤细胞(NOS-10、MG-63)。采用显微镜和流式细胞术评估NIR-PIT后的细胞死亡情况,采用肿瘤大小的纵向测量和组织学观察来评估NIR-PIT对异种移植瘤模型的影响。结果NIR-PIT后的thd -1染色证实了显微镜观察到的形态学改变(肿胀和泡形成)和细胞死亡。流式细胞术证实NIR-PIT后死细胞显著增加。在实验第10天,小鼠模型的肿瘤生长明显受到抑制,并且在组织学上观察到pit处理小鼠的肿瘤组织被破坏。结论NIR-PIT联合抗gd2抗体治疗神经母细胞瘤和骨肉瘤疗效显著。此外,NIR-PIT对神经母细胞瘤的治疗效果也通过小鼠体内模型得到验证。因此,临床应用应考虑进一步的实验和更有效的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Near-infrared photoimmunotherapy using antiGD2 antibody for neuroblastoma and osteosarcoma

Introduction

Near-infrared photoimmunotherapy (NIR-PIT) is a novel cancer therapy that specifically targets cancer cells. In NIR-PIT, antibody-photo-absorber-conjugates (APCs), specific for cancer antigens, target cancer cells. APCs that bind to antigens and are irradiated with NIR-light kill targeted cells. NIR-PIT has been clinically applied to head and neck squamous cell carcinoma in Japan, but not to pediatric cancers. Generally, neuroblastoma and osteosarcoma express disialoganglioside (GD2), making NIR-PIT that targets GD2 an additional treatment option.

Methods

Antihuman GD2 monoclonal antibody (clone 3F8) was conjugated with photo-absorber, IRDye 700DX (IR700). A human neuroblastoma cell (SK-N-SH) was used for in vitro and in vivo experiments, whereas human osteosarcoma cells (NOS-10, MG-63) were utilized for in vitro experiments. Microscopy and flow cytometry were used to evaluate cell death after NIR-PIT, and longitudinal measurement of tumor size and histological observation were utilized to assess the effect of NIR-PIT on the xenograft model.

Results

EthD-1 staining after NIR-PIT confirmed the morphological changes (swelling and bleb formation) observed by microscopy and cell death. Flow cytometry verified the significant increase in dead cells after NIR-PIT. Tumor growth in the mice model was significantly inhibited at day 10 of the experiment and destroyed tumor tissue was histologically observed in the PIT-treated mice.

Conclusion

The efficacy of NIR-PIT with antiGD2 antibody for neuroblastoma and osteosarcoma was indicated. Additionally, NIR-PIT efficacy against neuroblastoma was indicated by the mice model in vivo. Therefore, further experiments and more effective protocols should be considered for clinical application.
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