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靶向 TROP2 人源化抗体的胆胰肿瘤光免疫治疗

Photoimmunotherapy targeting biliary-pancreatic cancer with humanized anti-TROP2 antibody.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.

Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA.

出版信息

Cancer Med. 2019 Dec;8(18):7781-7792. doi: 10.1002/cam4.2658. Epub 2019 Nov 1.

Abstract

Photoimmunotherapy (PIT) is a new type of tumor-specific treatment utilizing monoclonal antibody (mAb)-photosensitizer conjugates and near-infrared (NIR) light irradiation. One potential PIT target, the type I transmembrane protein TROP2, is expressed at high levels in many cancers, including pancreatic carcinoma (PC) and cholangiocarcinoma (CC), in which its expression is correlated with poor prognosis and tumor aggressiveness. In this study, we assessed the efficacy of PIT utilizing newly developed humanized anti-TROP2 mAb conjugated to the photosensitizer IR700 (TROP2-IR700) for PC and CC. Immunohistochemistry on PC and CC tissue microarrays confirmed that TROP2 is overexpressed in about half of PC and CC specimens. Using cultured PC and CC cells, TROP2-IR700 localized TROP2-specific and target-specific cell killing was observed after NIR light irradiation. In addition, TROP2-IR700 was localized to mouse xenograft tumors expressing TROP2 after intravenous injection. PC and CC xenograft tumor growth was significantly inhibited by TROP2-targeted PIT relative to controls. The efficacy of TROP2-targeted PIT in vitro and against xenografted tumors in vivo suggests promise as a therapy for human PC and CC, both of which currently have dismal prognoses and limited therapeutic options.

摘要

光免疫疗法(PIT)是一种利用单克隆抗体(mAb)-光敏剂缀合物和近红外(NIR)光照射的新型肿瘤特异性治疗方法。一种潜在的 PIT 靶点,I 型跨膜蛋白 TROP2,在许多癌症中高水平表达,包括胰腺癌(PC)和胆管癌(CC),其表达与预后不良和肿瘤侵袭性相关。在这项研究中,我们评估了利用新开发的与人 TROP2 结合的光敏剂 IR700 (TROP2-IR700)对 PC 和 CC 的 PIT 疗效。对 PC 和 CC 组织微阵列的免疫组织化学证实,TROP2 在约一半的 PC 和 CC 标本中过表达。使用培养的 PC 和 CC 细胞,在 NIR 光照射后观察到 TROP2-IR700 定位的 TROP2 特异性和靶特异性细胞杀伤。此外,TROP2-IR700 在静脉注射后表达 TROP2 的小鼠异种移植肿瘤中被定位。与对照组相比,TROP2 靶向 PIT 显著抑制了 PC 和 CC 异种移植肿瘤的生长。TROP2 靶向 PIT 在体外的疗效和对异种移植肿瘤的作用提示其有望成为治疗人类 PC 和 CC 的一种方法,这两种癌症目前的预后均较差,治疗选择有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216a/6912056/8d03eb18cb7e/CAM4-8-7781-g001.jpg

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