TY - JOUR
T1 - Synthetic Rhamnose Glycopolymer Cell-Surface Receptor for Endogenous Antibody Recruitment
AU - De Coen, Ruben
AU - Nuhn, Lutz
AU - Perera, Chamani
AU - Arista-Romero, Maria
AU - Risseeuw, Martijn D.P.
AU - Freyn, Alec
AU - Nachbagauer, Raffael
AU - Albertazzi, Lorenzo
AU - Van Calenbergh, Serge
AU - Spiegel, David A.
AU - Peterson, Blake R.
AU - De Geest, Bruno G.
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2020/2/10
Y1 - 2020/2/10
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85078658353&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.9b01483
DO - 10.1021/acs.biomac.9b01483
M3 - Article
C2 - 31829561
AN - SCOPUS:85078658353
SN - 1525-7797
VL - 21
SP - 793
EP - 802
JO - Biomacromolecules
JF - Biomacromolecules
IS - 2
ER -