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使用固定化抗腺病毒抗体进行载体束缚的血管内微线圈基因递送。

Endovascular microcoil gene delivery using immobilized anti-adenovirus antibody for vector tethering.

作者信息

Abrahams John M, Song Cunxian, DeFelice Suzanne, Grady M Sean, Diamond Scott L, Levy Robert J

机构信息

Department of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, Pa 19104, USA.

出版信息

Stroke. 2002 May;33(5):1376-82. doi: 10.1161/01.str.0000014327.03964.c0.

Abstract

BACKGROUND AND PURPOSE

Endovascular microcoils are widely used in interventional procedures to treat cerebral aneurysms. In the present study we report for the first time successful use of an endovascular microcoil as a gene delivery system.

METHODS

Anti-adenoviral monoclonal antibodies were covalently attached to the collagen-coated surface of either platinum or polyglycolic acid microcoils. These antibodies were used to tether replication-deficient adenovirus (Ad-GFP [encoding green fluorescent protein] or Ad-LacZ [encoding beta-galactosidase]). Cell culture studies with rat arterial smooth muscle cells (A10) assessed transduction on or near the coil. Platinum coils coated with Ad-GFP were implanted into the ligated common carotid artery (CCA) of adult rats in a model of arterial stasis and pressurization. After 7 days, CCA segments were harvested, and coils were removed for histopathology and GFP expression studies, while organs were evaluated by polymerase chain reaction to assess viral biodistribution.

RESULTS

In cell culture studies, GFP-positive smooth muscle cells were detected only on the platinum coil surface, while LacZ-positive cells were detected only on the polyglycolic acid coil surface, thus demonstrating localized gene delivery. After 7-day implantation, GFP (according to fluorescence microscopy and confirmed with immunohistochemistry) was detected on the harvested platinum coil and in the organizing thrombus within the CCA but not in the arterial wall. Morphometric analyses revealed that 13.3+2.0% of cells within the organized thrombus were transduced with Ad-GFP via the gene delivery system. However, arterial smooth muscle cells were negative for GFP according to fluorescence microscopy and immunohistochemistry. Ad-GFP was not detectable by polymerase chain reaction in lung, liver, or kidney.

CONCLUSIONS

It is concluded that catheter deployment of platinum or biodegradable gene delivery endovascular microcoils represents an interventional device-based gene therapy system that can serve as a suitable platform for either single or multiple gene therapy vectors.

摘要

背景与目的

血管内微线圈广泛应用于介入治疗脑动脉瘤的手术中。在本研究中,我们首次报告了成功将血管内微线圈用作基因递送系统。

方法

抗腺病毒单克隆抗体共价连接到铂或聚乙醇酸微线圈的胶原包被表面。这些抗体用于连接复制缺陷型腺病毒(Ad-GFP[编码绿色荧光蛋白]或Ad-LacZ[编码β-半乳糖苷酶])。用大鼠动脉平滑肌细胞(A10)进行细胞培养研究,评估微线圈上或其附近的转导情况。将包被Ad-GFP的铂线圈植入成年大鼠结扎的颈总动脉(CCA),建立动脉淤滞和加压模型。7天后,采集CCA节段,取出线圈进行组织病理学和GFP表达研究,同时通过聚合酶链反应评估器官以确定病毒的生物分布。

结果

在细胞培养研究中,仅在铂线圈表面检测到GFP阳性平滑肌细胞,而仅在聚乙醇酸线圈表面检测到LacZ阳性细胞,从而证明了局部基因递送。植入7天后,在采集的铂线圈上以及CCA内的机化血栓中检测到GFP(根据荧光显微镜检查并经免疫组织化学证实),但动脉壁中未检测到。形态计量分析显示,通过基因递送系统,机化血栓内13.3+2.0%的细胞被Ad-GFP转导。然而,根据荧光显微镜检查和免疫组织化学,动脉平滑肌细胞GFP呈阴性。在肺、肝或肾中通过聚合酶链反应未检测到Ad-GFP。

结论

得出结论,铂或可生物降解的基因递送血管内微线圈的导管部署代表了一种基于介入装置的基因治疗系统,可作为单基因或多基因治疗载体的合适平台。

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