Intravascular Fluorescence Molecular Imaging of Inflammation in Atherosclerosis

动脉粥样硬化炎症的血管内荧光分子成像

• 批准号: 8259750
• 负责人: Farouc Amin Jaffer
• 金额: $ 43.18万
• 依托单位: MASSACHUSETTS GENERAL HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-15 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8259750
• 关键词: Angiography; Animals; Anti-Inflammatory Agents; Anti-inflammatory; Applications Grants; Arterial Fatty Streak; Arteries; Atherosclerosis; Biological; Biology; Blood; Calcium Chloride; Caliber; Cathepsins; Catheters; Clinic; Clinical; Collaborations; Collagen; Computer software; Confocal Microscopy; Control Animal; Coronary; Coronary artery; Custom; Detection; Development; Diagnosis; Diagnostic Imaging; Dose; Engineering; FDA approved; Family suidae; Fiber; Fibrin; Fluorescence; Fluorescence Microscopy; Fluorescent Dyes; Foundations; Fresh Frozen Plasmas; Goals; Human; Image; Imaging technology; Immunohistochemistry; Implant; In Vitro; Incubated; Indocyanine Green; Inflammation; Inflammatory; Injection of therapeutic agent; Laboratories; Lasers; Lead; Lipids; Manuals; Measures; Myocardial Infarction; Noise; Oryctolagus cuniculus; Peptide Hydrolases; Performance; Pharmacotherapy; Research Personnel; Research Project Grants; Resolution; Risk; Signal Transduction; Source; Staining method; Stains; Stents; Stratification; Stroke; Structure; System; Testing; Thrombin; Thrombus; Time; Translations; Treatment Efficacy; Ultrasonography; Vascular Diseases; Writing; base; design; design and construction; dosage; drug development; fluorescence imaging; high risk; image reconstruction; imaging modality; improved; in vivo; inflammatory marker; injured; molecular imaging; molecular/cellular imaging; multidisciplinary; nanoparticle; next generation; novel; public health relevance; research study; response; success; two-dimensional

DESCRIPTION (provided by applicant): New imaging methods are urgently needed to identify and to guide treatment of high-risk atherosclerotic plaques before lead to their devastating complications of myocardial infarction and stroke. While imaging technologies have made progress in illuminating plaque volume and plaque structure, they do not routinely visualize aspects of plaque biology such as inflammation, a key determinant of plaque complications. Imaging of molecular and cellular detail in atherosclerosis offers a transformative approach to improve the biological diagnosis, risk stratification, and treatment of high-risk plaques. In addition, molecular imaging of atherosclerosis can identify new pharmacotherapies that favorably alter plaque biology (e.g. anti-inflammatory), with the potential to streamline drug development and to efficiently bring new therapies into the clinic. At present however, existing molecular imaging approaches are unable to routinely visualize high-risk plaques in human coronary arteries. The long-term objective of this grant proposal is to develop new human coronary artery-targeted intravascular near-infrared fluorescence (NIRF) molecular imaging strategies to identify atherosclerotic plaques responsible for myocardial infarction. Recently, a one-dimensional, manual pullback intravascular NIRF sensing catheter established the feasibility of imaging plaque inflammation through blood in coronary-sized vessels. The Proposal now aims to develop a next-generation intravascular NIRF catheter capable of true two- dimensional NIRF imaging in human coronary-sized arteries in vivo. Specific Aim 1 will design, construct, and validate a rotational and automated pullback NIRF catheter to enable 360-degree and longitudinal 2D vessel wall imaging of atheroma inflammation in rabbit aortic vessels, an advance over existing limited-arc spectroscopic NIRF catheters. Specific Aim 2 will utilize the validated NIRF rotational catheter to assess anti- inflammatory (statin) effects in experimental atherosclerosis, extending the in vivo imaging armamentarium to assess the efficacy of therapeutics for vascular disease. Specific Aim 3 investigates the ability of indocyanine green, an FDA-approved diagnostic imaging agent, to serve as an inflammation-targeted intravascular NIRF imaging agent for atherosclerotic plaques. Specific Aim 4 tests the NIRF catheter's ability to perform molecular imaging directly in experimental coronary arteries in vivo, with the goal of accelerating catheter translation into the clinical arena. The Proposal builds on established large animal catheter-based imaging efforts in the Investigator's laboratory and leverages established engineering, imaging, and biological expertise from a multidisciplinary team. PUBLIC HEALTH RELEVANCE: New imaging methods are urgently needed to identify high-risk atherosclerotic plaques before they cause heart attacks. This research project is directed at developing new fluorescence catheters and approaches for imaging of high-risk plaques in human coronary-sized arteries. The results from this project could enable the development of clinical fluorescence imaging strategies to reduce heart attacks.

描述（由申请人提供）：迫切需要新的成像方法来识别和指导高危动脉粥样硬化斑块的治疗，以免导致心肌梗死和中风的毁灭性并发症。虽然成像技术在阐明斑块体积和斑块结构方面取得了进展，但它们不能常规地可视化斑块生物学的各个方面，例如炎症，这是斑块并发症的关键决定因素。 动脉粥样硬化的分子和细胞细节成像为改善高危斑块的生物学诊断、危险分层和治疗提供了一种变革性的方法。此外，动脉粥样硬化的分子成像可以识别有利于改变斑块生物学的新药物治疗（例如抗炎），有可能简化药物开发并有效地将新疗法引入临床。然而，目前，现有的分子成像方法无法常规地可视化人类冠状动脉中的高危斑块。 这项拨款提案的长期目标是开发新的人类冠状动脉靶向血管内近红外荧光（NIRF）分子成像策略，以识别导致心肌梗死的动脉粥样硬化斑块。最近，一维手动回拉血管内NIRF传感导管建立了通过冠状动脉大小的血管中的血液对斑块炎症进行成像的可行性。该提案现在旨在开发下一代血管内NIRF导管，该导管能够在体内人体冠状动脉大小的动脉中进行真正的二维NIRF成像。Specific Aim 1将设计、构建和验证旋转和自动回撤NIRF导管，以实现兔主动脉血管中粥样硬化炎症的360度和纵向2D血管壁成像，这是对现有有限弧光谱NIRF导管的进步。Specific Aim 2将利用经验证的NIRF旋转导管评估实验性动脉粥样硬化中的抗炎（他汀类药物）作用，扩展体内成像设备以评估血管疾病治疗的有效性。特定目标3研究了FDA批准的诊断成像剂吲哚菁绿色作为动脉粥样硬化斑块的炎症靶向血管内NIRF成像剂的能力。特定目标4测试了NIRF导管在体内实验冠状动脉中直接进行分子成像的能力，目的是加速导管进入临床竞技场。该提案建立在研究者实验室中已建立的大型动物基于导管的成像工作的基础上，并利用多学科团队已建立的工程、成像和生物学专业知识。 公共卫生相关性：迫切需要新的成像方法来识别高风险的动脉粥样硬化斑块，然后再引起心脏病发作。该研究项目旨在开发新的荧光导管和方法，用于对人类冠状动脉大小的动脉中的高危斑块进行成像。该项目的结果可以使临床荧光成像策略的发展，以减少心脏病发作。