| Literature DB >> 32524819 |
Bi Wang1, Simon Van Herck2, Yong Chen2, Xiangyang Bai1, Zifu Zhong3, Kim Deswarte4, Bart N Lambrecht4,5, Niek N Sanders3, Stefan Lienenklaus6, Hans W Scheeren1, Sunil A David7, Fabian Kiessling1, Twan Lammers1,8,9, Bruno G De Geest2, Yang Shi1.
Abstract
Synthetic immune-stimulatory drugs such as agonists of the Toll-like receptors (TLR) 7/8 are potent activators of antigen-presenting cells (APCs), however, they also induce severe side effects due to leakage from the site of injection into systemic circulation. Here, we report on the design and synthesis of an amphiphilic polymer-prodrug conjugate of an imidazoquinoline TLR7/8 agonist that in aqueous medium forms vesicular structures of 200 nm. The conjugate contains an endosomal enzyme-responsive linker enabling degradation of the vesicles and release of the TLR7/8 agonist in native form after endocytosis, which results in high in vitro TLR agonist activity. In a mouse model, locally administered vesicles provoke significantly more potent and long-lasting immune stimulation in terms of interferon expression at the injection site and in draining lymphoid tissue compared to a nonamphiphilic control and the native TLR agonist. Moreover, the vesicles induce robust activation of dendritic cells in the draining lymph node in vivo.Entities:
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Year: 2020 PMID: 32524819 PMCID: PMC7116109 DOI: 10.1021/jacs.0c01928
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419