单克隆抗体
超顺磁性
抗体
CD3型
生物物理学
化学
氧化铁纳米粒子
体内
抗原
核磁共振
分子生物学
氧化铁
病理
材料科学
生物
免疫学
医学
物理
磁化
CD8型
量子力学
有机化学
生物技术
磁场
作者
Alessandro Luchetti,Davide Milani,Francesca Ruffini,Rossella Galli,Andrea Falini,Angelo Quattrini,Giuseppe Scotti,Giacomo P. Comi,Gianvito Martino,Roberto Furlan,Letterio S. Politi
出处
期刊:Molecular Imaging
[SAGE Publishing]
日期:2012-03-01
卷期号:11 (2)
被引量:19
标识
DOI:10.2310/7290.2011.00032
摘要
We investigated the potential of antibody-vectorialized superparamagnetic iron oxide (SPIO) particles as cellular specific magnetic resonance contrast agents to image lymphocyte populations within the central nervous system (CNS), with the final goal of obtaining a reliable tool for noninvasively detecting and tracking specific cellular populations in vivo. We used superparamagnetic particles bound to a monoclonal antibody. The particle is the contrast agent, by means of its T₂* relaxation properties; the antibody is the targeting vector, responsible for homing the particle to target a surface antigen. To investigate the efficiency of particle vectorialization by these antibodies, we compared two types of antibody-vectorialized CD3-specific particles in vivo. We successfully employed vectorialized SPIO particles to image B220⁺ cells in a murine model of B-cell lymphoma. Likewise, we were able to identify CD3⁺ infiltrates in a murine model of multiple sclerosis. The specificity of the technique was confirmed by immunohistochemistry and electron microscopy of corresponding sections. Our findings suggest that indirect binding of the antibody to a streptavidinated particle allows for enhanced particle vectorialization compared to covalent binding of the antibody to the particle.
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