In vivo magnetic resonance imaging of acute brain inflammation using microparticles of iron oxide

被引:205
作者
McAteer, Martina A.
Sibson, Nicola R.
von zur Muhlen, Constantin
Schneider, Jurgen E.
Lowe, Andrew S.
Warrick, Nicholas
Channon, Keith M.
Anthony, Daniel C.
Choudhury, Robin P. [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Dept Cardiovasc Med, Oxford OX3 9DU, England
[2] Dept Physiol Anat & Genet, Expt Neuroimaging Grp, Oxford OX1 3PT, England
[3] Dept Pharmacol, Oxford OX1 3QX, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1038/nm1631
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multiple sclerosis is a disease of the central nervous system that is associated with leukocyte recruitment and subsequent inflammation, demyelination and axonal loss. Endothelial vascular cell adhesion molecule- 1 ( VCAM- 1) and its ligand, alpha(4)beta(1) integrin, are key mediators of leukocyte recruitment, and selective inhibitors that bind to the alpha(4) subunit of alpha(4)beta(1) substantially reduce clinical relapse in multiple sclerosis. Urgently needed is a molecular imaging technique to accelerate diagnosis, to quantify disease activity and to guide specific therapy. Here we report in vivo detection of VCAM- 1 in acute brain inflammation, by magnetic resonance imaging in a mouse model, at a time when pathology is otherwise undetectable. Antibody- conjugated microparticles carrying a large amount of iron oxide provide potent, quantifiable contrast effects that delineate the architecture of activated cerebral blood vessels. Their rapid clearance from blood results in minimal background contrast. This technology is adaptable to monitor the expression of endovascular molecules in vivo in various pathologies.
引用
收藏
页码:1253 / 1258
页数:6
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