Your browser doesn't support javascript.
loading
Synthetic Rhamnose Glycopolymer Cell-Surface Receptor for Endogenous Antibody Recruitment.
De Coen, Ruben; Nuhn, Lutz; Perera, Chamani; Arista-Romero, Maria; Risseeuw, Martijn D P; Freyn, Alec; Nachbagauer, Raffael; Albertazzi, Lorenzo; Van Calenbergh, Serge; Spiegel, David A; Peterson, Blake R; De Geest, Bruno G.
Afiliación
  • De Coen R; Department of Pharmaceutics , Ghent University , 9000 Ghent , Belgium.
  • Nuhn L; Max Planck Institute for Polymer Research , 55128 Mainz , Germany.
  • Perera C; Higuchi Biosciences Center , University of Kansas , Lawrence , Kansas 66047 , United States.
  • Arista-Romero M; Nanoscopy for Nanomedicine Group, Institute for Bioengineering of Catalonia (IBEC) , The Barcelona Institute of Science and Technology (BIST) , 08028 Barcelona , Spain.
  • Risseeuw MDP; Department of Biomedical Engineering, Institute for Complex Molecular Systems (ICMS) , Eindhoven University of Technology , 5612AZ Eindhoven , The Netherlands.
  • Freyn A; Department of Pharmaceutics , Ghent University , 9000 Ghent , Belgium.
  • Nachbagauer R; Department of Microbiology , Icahn School of Medicine at Mount Sinai , New York , NY 10029 , United States.
  • Albertazzi L; Graduate School of Biomedical Sciences , Icahn School of Medicine at Mount Sinai , New York , New York 10029 , United States.
  • Van Calenbergh S; Department of Microbiology , Icahn School of Medicine at Mount Sinai , New York , NY 10029 , United States.
  • Spiegel DA; Nanoscopy for Nanomedicine Group, Institute for Bioengineering of Catalonia (IBEC) , The Barcelona Institute of Science and Technology (BIST) , 08028 Barcelona , Spain.
  • Peterson BR; Department of Biomedical Engineering, Institute for Complex Molecular Systems (ICMS) , Eindhoven University of Technology , 5612AZ Eindhoven , The Netherlands.
  • De Geest BG; Department of Pharmaceutics , Ghent University , 9000 Ghent , Belgium.
Biomacromolecules ; 21(2): 793-802, 2020 02 10.
Article en En | MEDLINE | ID: mdl-31829561
ABSTRACT
Synthetic materials capable of engineering the immune system are of great relevance in the fight against cancer to replace or complement the current monoclonal antibody and cell therapy-based immunotherapeutics. Here, we report on antibody recruiting glycopolymers (ARGPs). ARGPs consist of polymeric copies of a rhamnose motif, which can bind endogenous antirhamnose antibodies present in human serum. As a proof-of-concept, we have designed ARGPs with a lipophilic end group that efficiently inserts into cell-surface membranes. We validate the specificity of rhamnose to attract antibodies from human serum to the target cell surface and demonstrate that ARGPs outperform an analogous small-molecule compound containing only one single rhamnose motif. The ARGP concept opens new avenues for the design of potent immunotherapeutics that mark target cells for destruction by the immune system through antibody-mediated effector functions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Ramnosa / Receptores de Superficie Celular / Anticuerpos Monoclonales / Formación de Anticuerpos Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biomacromolecules Asunto de la revista: BIOLOGIA MOLECULAR Año: 2020 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Ramnosa / Receptores de Superficie Celular / Anticuerpos Monoclonales / Formación de Anticuerpos Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biomacromolecules Asunto de la revista: BIOLOGIA MOLECULAR Año: 2020 Tipo del documento: Article País de afiliación: Bélgica