ICAM-1 expression in autoimmune encephalitis visualized using magnetic resonance imaging

被引:107
作者
Sipkins, DA
Gijbels, K
Tropper, FD
Bednarski, M
Li, KCP
Steinman, L [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, MRS Res Ctr, Dept Radiol, Stanford, CA 94305 USA
关键词
magnetic resonance imaging (MRI); multiple sclerosis (MS); intracellular adhesion molecules (ICAM);
D O I
10.1016/S0165-5728(99)00248-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of leukocyte adhesion molecules in the intact brains of-mice with experimental autoimmune encephalitis (EAE) was visualized by Magnetic Resonance Imaging (MRI) through the use of anew, target-specific MR contrast agent. Antibody-conjugated paramagnetic liposomes (ACPLs) were designed to achieve in vivo targeting of molecules expressed on vascular endothelium, while providing sufficient signal enhancement at these sires for detection by MRI. ACPLs targeted to intercellular adhesion molecule-1 (ICAM-1), an endothelial leukocyte receptor upregulated on cerebral microvasculature during EAE, were administered to diseased mice. Fluorescence microscopy confirmed that fluorescently-tagged ACPLs were localized to central nervous system (CNS) microvasculature in a pattern consistent with ICAM-1 upregulation described immunohistochemically. High resolution MRI of mouse brains ex vivo demonstrated that ACPL binding conferred significant enhancement of signal intensity (SI) as compared to control images. These results suggest that ACPLs can be used as MRI contrast agents to visualize specific:molecules expressed on vascular endothelium during disease. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
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页码:1 / 9
页数:9
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