Near-infrared imaging of flare-up arthritis with native fluorochrome Cy5.5 and albumin-bound Cy5.5

Andreas Hansch , Ingrid Hilger , Oliver Frey , Dieter Sauner , Mieczyslaw Gajda , Michael Haas , Ansgar Malich , Joachim Böttcher , Rolf Bräuer , Werner A. Kaiser
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引用次数: 7

Abstract

The aim of the study was to visualize chronic experimental arthritis with near-infrared fluorescence imaging (NIRF) in a murine experimental arthritis model of rheumatoid arthritis (RA) (flare-up arthritis). The flare-up arthritis model is a modification of the primary antigen-induced arthritis (AIA) model. NIRF was done for two preparations of the fluorochrome Cy5.5, one native and the other albumin conjugated. Histological features of flare-up arthritis were evaluated.

AIA was induced in 16 mice (strain C57/Bl6); flare-up arthritis was induced in a subgroup of eight. On day 7 after induction of flare-up arthritis, four mice received 50 nmol/kg native dye and four mice equimolar concentrations of the dye as albumin-dye conjugate intravenously. NIRF imaging was performed immediately before injection (baseline) and until 72 h thereafter. Arthritis severity was evaluated histologically for primary AIA and flare-up arthritis mice.

NIRF imaging revealed higher fluorochrome uptake in all inflamed knees compared to contralateral ones. The signal intensities induced by native Cy5.5 were higher than those generated by albumin–Cy5.5 conjugate. Histological evaluation of arthritic joints showed similar abnormalities in flare-up arthritis and in primary AIA joints.

Imaging of flare-up arthritis in the near-infrared range was successful for both fluorochrome preparations, but albumin conjugation prior to injection does not improve the uptake of dye in arthritic joints. Flare-up arthritis is a feasible model of chronic relapse of arthritis in human RA.

用天然荧光色素Cy5.5和白蛋白结合Cy5.5进行关节炎发作的近红外成像
该研究的目的是用近红外荧光成像(NIRF)在类风湿关节炎(RA)(突发关节炎)的小鼠实验关节炎模型中可视化慢性实验性关节炎。急性关节炎模型是对原发性抗原诱导关节炎(AIA)模型的改良。对两种制备的荧光色素Cy5.5进行了NIRF,一种是天然的,另一种是白蛋白偶联的。评估发作性关节炎的组织学特征。16只小鼠(C57/Bl6菌株)诱导AIA;在8个亚组中诱发了急性关节炎。在急性关节炎诱导后第7天,4只小鼠静脉注射50 nmol/kg天然染料和4只小鼠等摩尔浓度的白蛋白-染料偶联物。在注射前立即(基线)和注射后72小时进行NIRF成像。对原发性AIA和急性关节炎小鼠的关节炎严重程度进行组织学评估。近红外成像显示,与对侧膝盖相比,所有炎症膝盖的荧光素摄取更高。天然Cy5.5诱导的信号强度高于白蛋白- Cy5.5偶联物诱导的信号强度。关节炎关节的组织学评估显示,急性关节炎和原发性AIA关节有类似的异常。两种荧光染料制剂在近红外范围内对突发关节炎的成像都是成功的,但注射前的白蛋白偶联并不能改善关节炎关节对染料的吸收。发作性关节炎是人类风湿性关节炎慢性复发的一种可行模型。
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