| Literature DB >> 27312006 |
Roeland Lameris1, Renée C G de Bruin1, Paul M P van Bergen En Henegouwen2, Henk M Verheul1, Sonja Zweegman3, Tanja D de Gruijl1, Hans J van der Vliet1.
Abstract
Ligation of the CD1d antigen-presenting molecule by monoclonal antibodies (mAbs) can trigger important biological functions. For therapeutic purposes camelid-derived variable domain of heavy-chain-only antibodies (VHH) have multiple advantages over mAbs because they are small, stable and have low immunogenicity. Here, we generated 21 human CD1d-specific VHH by immunizing Lama glama and subsequent phage display. Two clones induced maturation of dendritic cells, one clone induced early apoptosis in CD1d-expressing B lymphoblasts and multiple myeloma cells, and another clone blocked recognition of glycolipid-loaded CD1d by CD1d-restricted invariant natural killer T (iNKT) cells. In contrast to reported CD1d-specific mAbs, these CD1d-specific VHH have the unique characteristic that they induce specific and well-defined biological effects. This feature, combined with the above-indicated general advantages of VHH, make the CD1d-specific VHH generated here unique and useful tools to exploit both CD1d ligation as well as disruption of CD1d-iNKT interactions in the treatment of cancer or inflammatory disorders.Entities:
Keywords: CD1d; cancer; dendritic cell; invariant natural killer T-cell; variable domain of heavy-chain-only antibody
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Year: 2016 PMID: 27312006 PMCID: PMC4981610 DOI: 10.1111/imm.12635
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397