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[11C](R)-PK11195正电子发射断层扫描成像在体内检测拉斯穆森脑炎中活化的小胶质细胞

[11C](R)-PK11195 positron emission tomography imaging of activated microglia in vivo in Rasmussen's encephalitis.

作者信息

Banati R B, Goerres G W, Myers R, Gunn R N, Turkheimer F E, Kreutzberg G W, Brooks D J, Jones T, Duncan J S

机构信息

MRC Cyclotron Unit, Imperial College School of Medicine, Hammersmith Hospital, London, UK.

出版信息

Neurology. 1999 Dec 10;53(9):2199-203. doi: 10.1212/wnl.53.9.2199.

Abstract

This study was designed to explore the feasibility of PET using 11C-PK11195 as an in vivo marker of activated microglia/brain macrophages for the assessment of neuroinflammation in Rasmussen's encephalitis (RE). 11C-PK11195 PET was carried out in four normal subjects, two patients with histologically confirmed RE, and three patients with clinically stable hippocampal sclerosis and low seizure frequency. Binding potential maps showing specific binding of 11C-PK11195 were generated for each subject. Regional binding potential values were calculated for anatomically defined regions of interest after coregistration to and spatial transformation into the subjects' own MRI. In one patient with RE who underwent hemispherectomy, the resected, paraffin-embedded brain tissue was stained with an antibody (CR3/43) that labels activated human microglia. Whereas specific binding of 11C-PK11195 in clinically stable hippocampal sclerosis was similar to that in normal brain, patients with RE showed a focal and diffuse increase in binding throughout the affected hemisphere. In RE, 11C-PK11195 PET can reveal in vivo the characteristic, unilateral pattern known from postmortem neuropathologic study. PET imaging of activated microglia/brain macrophages offers a tool for investigation of a range of brain diseases where neuroinflammation is a component and in which conventional MRI does not unequivocally indicate an inflammatory tissue reaction. 11C-PK11195 PET may help in the choice of appropriate biopsy sites and, further, may allow assessment of the efficacy of antiinflammatory disease-modifying treatment.

摘要

本研究旨在探讨使用11C-PK11195作为活化小胶质细胞/脑巨噬细胞的体内标志物进行正电子发射断层扫描(PET)以评估拉斯穆森脑炎(RE)神经炎症的可行性。对4名正常受试者、2名经组织学确诊为RE的患者以及3名临床稳定的海马硬化且癫痫发作频率较低的患者进行了11C-PK11195 PET检查。为每位受试者生成了显示11C-PK11195特异性结合的结合潜能图。在与受试者自身的磁共振成像(MRI)进行配准并进行空间变换后,计算了解剖学定义的感兴趣区域的区域结合潜能值。在一名接受了大脑半球切除术的RE患者中,对切除的石蜡包埋脑组织用标记活化人类小胶质细胞的抗体(CR3/43)进行染色。临床稳定的海马硬化患者中11C-PK11195的特异性结合与正常脑相似,而RE患者在整个受影响半球的结合呈现局灶性和弥漫性增加。在RE中,11C-PK11195 PET可以在体内揭示死后神经病理学研究中已知的特征性单侧模式。活化小胶质细胞/脑巨噬细胞的PET成像为研究一系列神经炎症是其中一个组成部分且传统MRI不能明确显示炎症组织反应的脑部疾病提供了一种工具。11C-PK11195 PET可能有助于选择合适的活检部位,并且进一步可能允许评估抗炎疾病修饰治疗的疗效。

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