Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169

被引:306
作者
Chen, Weihsu C. [1 ,2 ]
Kawasaki, Norihito [1 ,2 ]
Nycholat, Corwin M. [1 ,2 ]
Han, Shoufa [1 ,2 ]
Pilotte, Julie [1 ,2 ]
Crocker, Paul R. [3 ]
Paulson, James C. [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[3] Univ Dundee, Coll Life Sci, Wellcome Trust Bioctr, Dundee, Scotland
来源
PLOS ONE | 2012年 / 7卷 / 06期
基金
美国国家卫生研究院;
关键词
LYMPH-NODE; B-CELLS; RECEPTOR SIALOADHESIN; IMMUNE-RESPONSES; BINDING-RECEPTOR; DENDRITIC CELLS; IN-VITRO; T-CELLS; LEWIS-X; LIGANDS;
D O I
10.1371/journal.pone.0039039
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sialoadhesin (Sn, Siglec-1, CD169) is a member of the sialic acid binding Ig-like lectin (siglec) family expressed on macrophages. Its macrophage specific expression makes it an attractive target for delivering antigens to tissue macrophages via Sn-mediated endocytosis. Here we describe a novel approach for delivering antigens to macrophages using liposomal nanoparticles displaying high affinity glycan ligands of Sn. The Sn-targeted liposomes selectively bind to and are internalized by Sn-expressing cells, and accumulate intracellularly over time. Our results show that ligand decorated liposomes are specific for Sn, since they are taken up by bone marrow derived macrophages that are derived from wild type but not Sn-/- mice. Importantly, the Sn-targeted liposomes dramatically enhance the delivery of antigens to macrophages for presentation to and proliferation of antigen-specific T cells. Together, these data provide insights into the potential of cell-specific targeting and delivery of antigens to intracellular organelles of macrophages using Sn-ligand decorated liposomal nanoparticles.
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页数:9
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