The co-application of nectin-1 and PRV gD monoclonal antibodies: An effective approach to block pseudorabies virus invasion

IF 1.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS
Journal of virological methods Pub Date : 2026-02-01 Epub Date: 2025-10-12 DOI:10.1016/j.jviromet.2025.115271
Yumei Chen , Haonan Wang , Jingming Zhou , Chao Liang , Hongliang Liu , Sixuan Wu , Yanhua Qi , Xifang Zhu , Enping Liu , Aiping Wang
{"title":"The co-application of nectin-1 and PRV gD monoclonal antibodies: An effective approach to block pseudorabies virus invasion","authors":"Yumei Chen ,&nbsp;Haonan Wang ,&nbsp;Jingming Zhou ,&nbsp;Chao Liang ,&nbsp;Hongliang Liu ,&nbsp;Sixuan Wu ,&nbsp;Yanhua Qi ,&nbsp;Xifang Zhu ,&nbsp;Enping Liu ,&nbsp;Aiping Wang","doi":"10.1016/j.jviromet.2025.115271","DOIUrl":null,"url":null,"abstract":"<div><div>Pseudorabies virus (PRV), a zoonotic alphaherpesvirus threatening swine industries and human health, exploits glycoprotein D (gD)-nectin-1 interactions for host cell entry. Here, we report a dual-target neutralizing strategy combining a novel gD-specific monoclonal neutralization antibody (3F7) with nectin-1-blocking mAb. In vitro neutralization assays demonstrated that 3F7 alone achieved potent cross-species inhibition of PRV infection in porcine kidney cells (PK15), human neuroblastoma cells (SK-N-SH), and human embryonic kidney cells (HEK 293 T) (IC<sub>50</sub>: 0.56–5.39 μg/mL). Co-administration with nectin-1-targeting mAb synergistically enhanced neutralization efficacy by 0.9–25.8 %, revealing a cooperative mechanism between viral glycoprotein blockade and host receptor interference. This study presents the initial evidence indicating that antibodies targeting both the pathogen and its host entry factor, nectin-1, significantly enhance the anti-PRV activity. These findings highlight a novel and effective strategy for mitigating zoonotic PRV transmission, especially among high-risk populations such as swine workers. Moreover, the study provides a promising avenue for the development of next-generation biologics against emerging zoonotic herpesviruses, offering significant implications for both veterinary and human public health.</div></div>","PeriodicalId":17663,"journal":{"name":"Journal of virological methods","volume":"340 ","pages":"Article 115271"},"PeriodicalIF":1.7000,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of virological methods","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166093425001648","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Pseudorabies virus (PRV), a zoonotic alphaherpesvirus threatening swine industries and human health, exploits glycoprotein D (gD)-nectin-1 interactions for host cell entry. Here, we report a dual-target neutralizing strategy combining a novel gD-specific monoclonal neutralization antibody (3F7) with nectin-1-blocking mAb. In vitro neutralization assays demonstrated that 3F7 alone achieved potent cross-species inhibition of PRV infection in porcine kidney cells (PK15), human neuroblastoma cells (SK-N-SH), and human embryonic kidney cells (HEK 293 T) (IC50: 0.56–5.39 μg/mL). Co-administration with nectin-1-targeting mAb synergistically enhanced neutralization efficacy by 0.9–25.8 %, revealing a cooperative mechanism between viral glycoprotein blockade and host receptor interference. This study presents the initial evidence indicating that antibodies targeting both the pathogen and its host entry factor, nectin-1, significantly enhance the anti-PRV activity. These findings highlight a novel and effective strategy for mitigating zoonotic PRV transmission, especially among high-risk populations such as swine workers. Moreover, the study provides a promising avenue for the development of next-generation biologics against emerging zoonotic herpesviruses, offering significant implications for both veterinary and human public health.
联合应用Nectin-1和PRV gD单克隆抗体:阻断伪狂犬病毒侵袭的有效方法
伪狂犬病毒(PRV)是一种威胁养猪业和人类健康的人畜共患甲型疱疹病毒,利用糖蛋白D (gD)-连接蛋白-1相互作用进入宿主细胞。在这里,我们报道了一种双靶点中和策略,结合了一种新的gd特异性单克隆中和抗体(3F7)和nectin-1阻断单抗。体外中和实验表明,3F7对猪肾细胞(PK15)、人神经母细胞瘤细胞(SK-N-SH)和人胚胎肾细胞(HEK 293T)的PRV感染具有明显的跨种抑制作用(IC50: 0.56 ~ 5.39μg/mL)。与以nectin-1为靶点的mAb共给药可协同提高14.5-25.8%的中和效果,揭示了病毒糖蛋白阻断与宿主受体干扰之间的协同机制。本研究提供了初步证据,表明针对病原体及其宿主进入因子nectin-1的抗体可显著增强抗prv活性。这些发现强调了一种减轻人畜共患PRV传播的新颖而有效的策略,特别是在猪工人等高危人群中。此外,该研究为开发针对新出现的人畜共患疱疹病毒的下一代生物制剂提供了一条有希望的途径,对兽医和人类公共卫生都具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书