| Literature DB >> 30088325 |
Xuan Liu1, Lunzhi Yuan2, Liang Zhang2, Yalin Mu1, Xiaoling Li2, Chao Liu1, Peng Lv1, Yali Zhang2, Tong Cheng2, Quan Yuan2, Ningshao Xia2, Xiaoyuan Chen3, Gang Liu1,4.
Abstract
A facile route is presented for fabricating a new class of nanomimics that overexpress hepatitis B virus (HBV) receptor by a natural biosynthetic procedure against HBV infection. A nine-transmembrane HBV-specific receptor, human sodium taurocholate co-transporting polypeptide (hNTCP), was engineered to naturally immobilize it onto the cellular surface and subsequently trigger the budding of hNTCP-anchoring membrane vesicles (hNTCP-MVs) that favor the HBV virion. hNTCP-MVs could rapidly block HBV infection in cell models. Furthermore, hNTCP-MVs treatment could effectively prevent viral infection, spreading, and replication in a human-liver-chimeric mouse model of HBV infection. Our findings demonstrate the receptor-mediated antiviral effect of hNTCP-MVs to trick HBV and offer novel opportunities for further development of antiviral strategies in nanomedicine.Entities:
Keywords: hepatitis B; infection inhibition; nanomedicine; nanovesicles; receptors
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Year: 2018 PMID: 30088325 PMCID: PMC6447037 DOI: 10.1002/anie.201807212
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336