4.5 Article

Assessment of the enhancement of PLGA nanoparticle uptake by dendritic cells through the addition of natural receptor ligands and monoclonal antibody

期刊

VACCINE
卷 33, 期 48, 页码 6588-6595

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2015.10.093

关键词

Nanopartide; Targeting; Mannose; Cattle; Dendritic cell; DEC-205 antibody

资金

  1. APHA Research and Development Internal Investment Fund [SC0200]
  2. Department for the Environment, Food and Rural Affairs, UK [OD0345]
  3. Biotechnology and Biological Sciences Research Council [BBS/E/I/00001715, BBS/E/I/00002035] Funding Source: researchfish
  4. BBSRC [BBS/E/I/00002035, BBS/E/I/00001715] Funding Source: UKRI

向作者/读者索取更多资源

Targeting of specific receptors on antigen-presenting cells is an appealing prospect in the production of novel nanoparticulate vaccines. In particular, the targeting of vaccines to dendritic cell (DC) subsets has been shown in models to significantly improve the induction of immune responses. This paper describes the evaluation of natural ligands, mannan and chitosan, and monoclonal antibodies as targeting motifs to enhance uptake of PLGA nanoparticle carriers by bovine DCs. To assess enhancement of uptake after the addition of natural ligands a bovine monocyte derived DC (MoDC) model was used. For the assessment of monoclonal antibody targeting, the model was expanded to include afferent lymph DCs (ALDCs) in a competitive uptake assay. Mannan, proved unsuccessful at enhancing uptake or targeting by MoDCs. Chitosan coated particle uptake could be impeded by the addition of mannan suggesting uptake may be mediated through sugar receptors. Inclusion of monoclonal antibodies specific for the DEC-205 (CD205) receptor increased the number of receptor expressing DCs associated with particles as well as the number of particles taken up by individual cells. These results support the further evaluation of active targeting of nanovaccines to DCs to enhance their immunogenicity in cattle and other large mammalian species including humans. Crown Copyright (C) 2015 Published by Elsevier Ltd. All rights reserved.

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