| Literature DB >> 31829561 |
Ruben De Coen1, Lutz Nuhn2, Chamani Perera3, Maria Arista-Romero4,5, Martijn D P Risseeuw1, Alec Freyn6,7, Raffael Nachbagauer6, Lorenzo Albertazzi4,5, Serge Van Calenbergh1, David A Spiegel8, Blake R Peterson9, Bruno G De Geest1.
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.Entities:
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Year: 2020 PMID: 31829561 DOI: 10.1021/acs.biomac.9b01483
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988