Antigen delivery to macrophages using liposomal nanoparticles targeting Sialoadhesin/CD169

W.C. Chen, N. Kawasaki, C.M. Nycholat, S. Han, J. Pilotte, P.R. Crocker, J.C. Paulson

    Research output: Contribution to journalArticlepeer-review

    103 Citations (Scopus)

    Abstract

    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.
    Original languageEnglish
    Article numbere39039
    JournalPLoS ONE
    Volume7
    Issue number6
    DOIs
    Publication statusPublished - 19 Jun 2012

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