PLoS ONE · 2012 · 117 citations · 41 references
PharmacyImmunologyPharmaceuticsDrug DeliveryEndocytosisInnate ImmunityLiposomal FormulationsLiposome-based DeliveryMacrophage BiologyNanomedicineNanoparticle Delivery SystemsTargeting LigandsCell-specific TargetingCellular Uptake Of LiposomesLiposomal Delivery SystemsLiposomal NanocarriersLiposomesNanoparticle-based Macrophage TargetingNanoparticlesTargeted Liposomes
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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CD24 and Siglec-10 Selectively Repress Tissue Damage–Induced Immune Responses
Guo‐Yun Chen, Jie Tang, Pan Zheng et al. · Science · 2009 · 777 citations · Full text
Kenichi Asano, Ami Nabeyama, Yasunobu Miyake et al. · Immunity · 2010 · 444 citations · Full text
Life Sciences, Immunology, Oncology +14