Selective Uptake of Cylindrical Poly(2‐Oxazoline) Brush‐AntiDEC205 Antibody‐OVA Antigen Conjugates into DEC‐Positive Dendritic Cells and Subsequent T‐Cell Activation |
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Authors: | Dr. Jasmin Bühler Sabine Gietzen Dr. Anika Reuter Cinja Kappel Dr. Karl Fischer Sandra Decker David Schäffel Dr. Kaloian Koynov Dr. Matthias Bros Ingrid Tubbe Dr. Stephan Grabbe Dr. Manfred Schmidt |
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Affiliation: | 1. Institute for Physical Chemistry, University of Mainz, Jakob‐Welder Weg 11, 55099 Mainz (Germany);2. Graduate School Materials Science, Staudinger Weg 9, 55128 Mainz (Germany);3. Max Planck Graduate Center, Staudinger Weg 9, 55128 Mainz (Germany);4. Department of Dermatology, University Medical Center of the Johannes Gutenberg, University Mainz, Langenbeckstrasse 1, 55131 Mainz (Germany);5. Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz (Germany) |
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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. |
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Keywords: | brush polymers cancer therapy dendritic cells nanocarriers T‐cells |
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