Department of Radiology, Molecular Imaging Program at Stanford, Stanford, California.
Department of Health, Research and Policy, Stanford University, Stanford, California.
Clin Cancer Res. 2018 Apr 1;24(7):1574-1585. doi: 10.1158/1078-0432.CCR-17-2057. Epub 2018 Jan 4.
To engineer a dual human and murine Thy1-binding single-chain-antibody ligand (Thy1-scFv) for contrast microbubble-enhanced ultrasound molecular imaging of pancreatic ductal adenocarcinoma (PDAC). Thy1-scFv were engineered using yeast-surface-display techniques. Binding to soluble human and murine Thy1 and to Thy1-expressing cells was assessed by flow cytometry. Thy1-scFv was then attached to gas-filled microbubbles to create MB Thy1 binding of MB to Thy1-expressing cells was evaluated under flow shear stress conditions in flow-chamber experiments. MB and MB were used as negative controls. All microbubble types were tested in both orthotopic human PDAC xenografts and transgenic PDAC mice Thy1-scFv had a of 3.4 ± 0.36 nmol/L for human and 9.2 ± 1.7 nmol/L for murine Thy1 and showed binding to both soluble and cellularly expressed Thy1. MB was attached to Thy1 with high affinity compared with negative control microbubbles ( < 0.01) as assessed by flow cytometry. Similarly, flow-chamber studies showed significantly ( < 0.01) higher binding of MB (3.0 ± 0.81 MB/cell) to Thy1-expressing cells than MB (0.57 ± 0.53) and MB (0.43 ± 0.53). ultrasound molecular imaging using MB demonstrated significantly higher signal ( < 0.01) in both orthotopic (5.32 ± 1.59 a.u.) and transgenic PDAC (5.68 ± 2.5 a.u.) mice compared with chronic pancreatitis (0.84 ± 0.6 a.u.) and normal pancreas (0.67 ± 0.71 a.u.). immunofluorescence confirmed significantly ( < 0.01) increased Thy1 expression in PDAC compared with chronic pancreatitis and normal pancreas tissue. A dual human and murine Thy1-binding scFv was designed to generate contrast microbubbles to allow PDAC detection with ultrasound. .
为了对胰腺导管腺癌 (PDAC) 进行对比微泡增强超声分子成像,我们设计了一种与人源和鼠源 Thy1 结合的单链抗体配体 (Thy1-scFv)。采用酵母表面展示技术构建 Thy1-scFv。通过流式细胞术评估其与人源和鼠源可溶性 Thy1 以及表达 Thy1 的细胞的结合能力。然后,将 Thy1-scFv 连接到充入气体的微泡上,在流动室实验中评估微泡在流动剪切应力条件下与表达 Thy1 的细胞的结合能力。使用 MB 作为阴性对照。所有微泡类型均在原位人源 PDAC 异种移植瘤和转基因 PDAC 小鼠中进行了测试。Thy1-scFv 与人源 Thy1 的结合亲和力为 3.4±0.36nmol/L,与鼠源 Thy1 的结合亲和力为 9.2±1.7nmol/L,且能与可溶性和细胞表面表达的 Thy1 结合。流式细胞术评估结果表明,与阴性对照微泡相比,MB 与人源 Thy1 的结合具有更高的亲和力(<0.01)。同样,流动室研究表明,MB 与人源 Thy1 表达细胞的结合明显(<0.01)高于 MB(0.57±0.53)和 MB(0.43±0.53)。使用 MB 进行超声分子成像在原位和转基因 PDAC 小鼠中均显示出显著更高的信号(<0.01)(分别为 5.32±1.59a.u.和 5.68±2.5a.u.),与慢性胰腺炎(0.84±0.6a.u.)和正常胰腺(0.67±0.71a.u.)相比。免疫荧光证实,PDAC 中 Thy1 的表达明显高于慢性胰腺炎和正常胰腺组织(<0.01)。我们设计了一种与人源和鼠源 Thy1 结合的 scFv,用于生成对比微泡,以实现 PDAC 的超声检测。