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利用双光子显微镜进行活体成像以评估抗 CD137 开关抗体的肿瘤选择性结合

英文原题:In vivo imaging with two-photon microscopy to assess the tumor-selective binding of an anti-CD137 switch antibody.

查看英文原题

In vivo imaging with two-photon microscopy to assess the tumor-selective binding of an anti-CD137 switch antibody.

PubMed 2022/03/22(内容时间) Sci Rep Q1 · IF 4.9(JCR 2025)

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中文摘要

STA551是一种新型抗CD137开关抗体,以细胞外ATP浓度依赖性方式与CD137结合。尽管推测STA551在肿瘤组织中的靶点结合高于正常组织,但在体内定量检测开关抗体的靶点结合在技术上具有挑战性。

在本研究中,我们利用双光子显微镜的活体成像技术研究了STA551在体内的靶点结合。荷瘤人CD137敲入小鼠经静脉注射荧光标记抗体。进行了抗体结合细胞的流式细胞术分析和双光子显微镜活体成像。流式细胞术分析检测到肿瘤中CD137表达高于脾组织,T细胞和NK细胞是主要的CD137表达细胞。在活体成像实验中,传统抗CD137抗体和开关抗CD137抗体在肿瘤中均显示结合。

然而,在脾脏中,开关抗体的荧光远弱于传统抗CD137抗体,与同型对照相当。总之,我们能够通过双光子显微镜活体成像评估开关抗体在体内的生物分布。这些结果表明,STA551的肿瘤选择性结合导致宽治疗窗和强效抗肿瘤疗效,而无需全身性免疫激活。

展开英文摘要原文

STA551, a novel anti-CD137 switch antibody, binds to CD137 in an extracellular ATP concentration-dependent manner. Although STA551 is assumed to show higher target binding in tumor tissues than in normal tissues, quantitative detection of the target binding of the switch antibody in vivo is technically challenging. In this study, we investigated the target binding of STA551 in vivo using intravital imaging with two-photon microscopy.

Tumor-bearing human CD137 knock-in mice were intravenously administered fluorescently labeled antibodies. Flow cytometry analysis of antibody-binding cells and intravital imaging using two-photon microscopy were conducted. Higher CD137 expression in tumor than in spleen tissues was detected by flow cytometry analysis, and T cells and NK cells were the major CD137-expressing cells. In the intravital imaging experiment, conventional and switch anti-CD137 antibodies showed binding in tumors.

However, in the spleen, the fluorescence of the switch antibody was much weaker than that of the conventional anti-CD137 antibody and comparable with that of the isotype control.

In conclusion, we were able to assess switch antibody biodistribution in vivo through intravital imaging with two-photon microscopy. These results suggest that the tumor-selective binding of STA551 leads to a wide therapeutic window and potent antitumor efficacy without systemic immune activation.

论文信息

作者
Kaneko C、Tsutsui H、Ozeki K、Honda M、Haraya K、Narita Y、Kamata-Sakurai M、Kikuta J
第一作者单位
Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135, Komakado, Gotemba, Shizuoka, 412-8513, Japan.Japan
通讯作者单位
Translational Research Division, Chugai Pharmaceutical Co., Ltd., 1-135, Komakado, Gotemba, Shizuoka, 412-8513, Japan. hondamsk@chugai-pharm.co.jp.Japan
期刊
Scientific reports2022 Mar 22
原文标识
PubMed 35318394 · DOI 10.1038/s41598-022-08951-1