A monoclonal antibody neutralizes pesudorabies virus by blocking gD binding to the receptor nectin-1

体内 病毒学 病毒 单克隆抗体 体外 抗体 伪狂犬病 分子生物学 受体 表位 生物 化学 免疫学 生物化学 生物技术
作者
Teng Zhang,Yunchao Liu,Yumei Chen,Jucai Wang,Hua Feng,Qiang Wei,Shuangshuang Zhao,Suzhen Yang,Dongmin Liu,Gaiping Zhang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:188: 359-368 被引量:11
标识
DOI:10.1016/j.ijbiomac.2021.07.170
摘要

Pseudorabies virus (PRV) was isolated from some human cases recently and the infected patients manifested respiratory dysfunction and acute neurological symptoms. However, no effective drug or vaccine, preventing the progression of PRV infection, is available. Nectin-1 was the only reported receptor for PRV cell entry both swine and human origin, representing an excellent target to block PRV infection, and especially its transmission from pigs to humans. A PRV-gD specific mAbs (10B6) was isolated from hybridomas and its neutralizing activities in vitro and in vivo were determined. 10B6 exhibited effective neutralizing activities in vitro with IC50 = 2.514 μg/ml and 4.297 μg/ml in the presence and absence of complement. And in vivo, 10B6 provided 100% protection against PRV lethal challenge with a dose of 15 mg/kg. Further, 10B6 could bind to a conserved epitope, 316QPAEPFP322, locating in gD pro-fusion domain, and finally blocks the binding of PRV-gD to nectin-1. Moreover, 10B6 showed an effective inhibition on PRV cell-attachment in a cell type-independent manner and could also block the virus spreading among cells. 10B6 exhibited effectively neutralizing activities to Chinese PRV variant strain in vitro and in vivo by blocking gD binding to nectin-1, implied both prophylactic and therapeutic interventions against PRV infections.
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