| Literature DB >> 25111768 |
Jasmin Bühler1, Sabine Gietzen, Anika Reuter, Cinja Kappel, Karl Fischer, Sandra Decker, David Schäffel, Kaloian Koynov, Matthias Bros, Ingrid Tubbe, Stephan Grabbe, Manfred Schmidt.
Abstract
To achieve specific cell targeting by various receptors for oligosaccharides or antibodies, a carrier must not be taken up by any of the very many different cells and needs functional groups prone to clean conjugation chemistry to derive well-defined structures with a high biological specificity. A polymeric nanocarrier is presented that consists of a cylindrical brush polymer with poly-2-oxazoline side chains carrying an azide functional group on each of the many side chain ends. After click conjugation of dye and an anti-DEC205 antibody to the periphery of the cylindrical brush polymer, antibody-mediated specific binding and uptake into DEC205(+) -positive mouse bone marrow-derived dendritic cells (BMDC) was observed, whereas binding and uptake by DEC205(-) negative BMDC and non-DC was essentially absent. Additional conjugation of an antigen peptide yielded a multifunctional polymer structure with a much stronger antigen-specific T-cell stimulatory capacity of pretreated BMDC than application of antigen or polymer-antigen conjugate.Entities:
Keywords: T-cells; brush polymers; cancer therapy; dendritic cells; nanocarriers
Mesh:
Substances:
Year: 2014 PMID: 25111768 DOI: 10.1002/chem.201403942
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236