Monoclonal Antibodies Conjugated with Superparamagnetic Iron Oxide Particles Allow Magnetic Resonance Imaging Detection of Lymphocytes in the Mouse Brain
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作者:
Luchetti, Alessandro
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Luchetti, Alessandro
Milani, Davide
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Milani, Davide
Ruffini, Francesca
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Ruffini, Francesca
Galli, Rossella
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Galli, Rossella
Falini, Andrea
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Falini, Andrea
Quattrini, Angelo
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Quattrini, Angelo
Scotti, Giuseppe
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Scotti, Giuseppe
Comi, Giancarlo
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Comi, Giancarlo
Martino, Gianvito
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Martino, Gianvito
Furlan, Roberto
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Furlan, Roberto
Politi, Letterio S.
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机构:Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
Politi, Letterio S.
机构:
[1] Ist Sci San Raffaele, Dept Clin Neuroimmunol, Stem Cell Res Inst, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, Dept Neurosurg, Stem Cell Res Inst, I-20132 Milan, Italy
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 T-2* 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.