Department of Microbiology-Immunology, Northwestern University, Feinberg School of Medicine, 6-713 Tarry Building, 303 E Chicago Avenue, Chicago, IL 60611, USA.
J Neuroinflammation. 2013 Nov 15;10:138. doi: 10.1186/1742-2094-10-138.
Experimental autoimmune encephalomyelitis (EAE) is an animal model that captures many of the hallmarks of human multiple sclerosis (MS), including blood-brain barrier (BBB) breakdown, inflammation, demyelination and axonal destruction. The standard clinical score measurement of disease severity and progression assesses functional changes in animal mobility; however, it does not offer information regarding the underlying pathophysiology of the disease in real time. The purpose of this study was to apply a novel optical imaging technique that offers the advantage of rapid imaging of relevant biomarkers in live animals.
Advances in non-invasive fluorescence molecular tomographic (FMT) imaging, in combination with a variety of biological imaging agents, offer a unique, sensitive and quantifiable approach to assessing disease biology in living animals. Using vascular (AngioSense 750EX) and protease-activatable cathepsin B (Cat B 680 FAST) near infrared (NIR) fluorescence imaging agents to detect BBB breakdown and inflammation, respectively, we quantified brain and spinal cord changes in mice with relapsing-remitting PLP139-151-induced EAE and in response to tolerogenic therapy.
FMT imaging and analysis techniques were carefully characterized and non-invasive imaging results corroborated by both ex vivo tissue imaging and comparison to clinical score results and histopathological analysis of CNS tissue. FMT imaging showed clear differences between control and diseased mice, and immune tolerance induction by antigen-coupled PLGA nanoparticles effectively blocked both disease induction and accumulation of imaging agents in the brain and spinal cord.
Cat B 680 FAST and AngioSense 750EX offered the combination best able to detect disease in both the brain and spinal cord, as well as the downregulation of disease by antigen-specific tolerance. Non-invasive optical tomographic imaging thus offers a unique approach to monitoring neuroinflammatory disease and therapeutic intervention in living mice with EAE.
实验性自身免疫性脑脊髓炎(EAE)是一种动物模型,可捕获人类多发性硬化症(MS)的许多特征,包括血脑屏障(BBB)破裂、炎症、脱髓鞘和轴突破坏。疾病严重程度和进展的标准临床评分测量评估动物活动能力的功能变化;然而,它不能实时提供有关疾病潜在病理生理学的信息。本研究的目的是应用一种新型光学成像技术,该技术具有在活体动物中快速成像相关生物标志物的优势。
非侵入性荧光分子断层扫描(FMT)成像的进步,结合各种生物成像剂,为评估活体动物疾病生物学提供了一种独特、敏感和可量化的方法。使用血管(AngioSense 750EX)和蛋白酶可激活的组织蛋白酶 B(Cat B 680 FAST)近红外(NIR)荧光成像剂分别检测 BBB 破裂和炎症,我们量化了复发缓解型 PLP139-151 诱导的 EAE 小鼠以及对耐受原性治疗的脑和脊髓变化。
仔细描述了 FMT 成像和分析技术,并通过离体组织成像以及与临床评分结果和中枢神经系统组织的组织病理学分析进行比较,证实了非侵入性成像结果。FMT 成像显示了对照组和患病组小鼠之间的明显差异,抗原偶联 PLGA 纳米颗粒诱导的免疫耐受有效地阻止了疾病的诱导和成像剂在大脑和脊髓中的积累。
Cat B 680 FAST 和 AngioSense 750EX 提供了能够在大脑和脊髓中检测疾病以及通过抗原特异性耐受下调疾病的最佳组合。非侵入性光学断层扫描成像因此为监测活体 EAE 小鼠的神经炎症性疾病和治疗干预提供了一种独特的方法。