A monoclonal antibody targeting the Nipah virus fusion glycoprotein apex imparts protection from disease

亨德拉病毒 单克隆抗体 病毒学 抗体 生物 表位 糖蛋白 病毒 埃博拉病毒 接种疫苗 融合蛋白 免疫学 分子生物学 生物化学 基因 重组DNA
作者
Victoria A. Avanzato,Trenton Bushmaker,Kasopefoluwa Y. Oguntuyo,Claude Kwe Yinda,Helen M. E. Duyvesteyn,Robert Stass,Kimberly Meade‐White,Rebecca Rosenke,Tina Thomas,Neeltje van Doremalen,Greg Saturday,Katie J. Doores,Benhur Lee,Thomas A. Bowden,Vincent J. Munster
出处
期刊:Journal of Virology [American Society for Microbiology]
标识
DOI:10.1128/jvi.00638-24
摘要

ABSTRACT Nipah virus (NiV) is a highly pathogenic paramyxovirus capable of causing severe respiratory and neurologic disease in humans. Currently, there are no licensed vaccines or therapeutics against NiV, underscoring the urgent need for the development of countermeasures. The NiV surface-displayed glycoproteins, NiV-G and NiV-F, mediate host cell attachment and fusion, respectively, and are heavily targeted by host antibodies. Here, we describe a vaccination-derived neutralizing monoclonal antibody, mAb92, that targets NiV-F. Structural characterization of the Fab region bound to NiV-F (NiV-F–Fab92) by cryo-electron microscopy analysis reveals an epitope in the DIII domain at the membrane distal apex of NiV-F, an established site of vulnerability on the NiV surface. Further, prophylactic treatment of hamsters with mAb92 offered complete protection from NiV disease, demonstrating beneficial activity of mAb92 in vivo . This work provides support for targeting NiV-F in the development of vaccines and therapeutics against NiV. IMPORTANCE Nipah virus (NiV) is a highly lethal henipavirus (HNV) that causes severe respiratory and neurologic disease in humans. Currently, there are no licensed vaccines or therapeutics against NiV, highlighting a need to develop countermeasures. The NiV surface displays the receptor binding protein (NiV-G, or RBP) and the fusion protein (NiV-F), which allow the virus to attach and enter cells. These proteins can be targeted by vaccines and antibodies to prevent disease. This work describes a neutralizing antibody (mAb92) that targets NiV-F. Structural characterization by cryo-electron microscopy analysis reveals where the antibody binds to NiV-F to neutralize the virus. This study also shows that prophylactic treatment of hamsters with mAb92 completely protected against developing NiV disease. This work shows how targeting NiV-F can be useful to preventing NiV disease, supporting future studies in the development of vaccines and therapeutics.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
尔玉完成签到 ,获得积分10
1秒前
5秒前
6秒前
帅气的沧海完成签到 ,获得积分10
7秒前
7秒前
Cu完成签到 ,获得积分10
8秒前
ran完成签到 ,获得积分10
8秒前
温暖完成签到 ,获得积分10
9秒前
雷锋完成签到 ,获得积分10
10秒前
xuxu发布了新的文献求助10
11秒前
张北北发布了新的文献求助10
12秒前
陶醉书包完成签到 ,获得积分10
13秒前
zijingsy完成签到 ,获得积分10
14秒前
科目三应助科研通管家采纳,获得10
17秒前
FashionBoy应助科研通管家采纳,获得10
17秒前
bkagyin应助科研通管家采纳,获得10
17秒前
kong应助科研通管家采纳,获得10
17秒前
今后应助科研通管家采纳,获得10
17秒前
17秒前
ding应助科研通管家采纳,获得10
17秒前
zxzb完成签到,获得积分10
18秒前
肥而不腻的羚羊完成签到,获得积分10
21秒前
xuxu关注了科研通微信公众号
23秒前
月月完成签到,获得积分10
23秒前
无忧无虑完成签到 ,获得积分10
31秒前
xyzlancet完成签到,获得积分10
35秒前
张北北完成签到,获得积分20
39秒前
zcc完成签到,获得积分10
39秒前
麻黄阿葵完成签到,获得积分10
40秒前
livra1058完成签到,获得积分10
41秒前
拼搏的青雪完成签到 ,获得积分10
42秒前
蓝豆子完成签到 ,获得积分10
44秒前
宇文青寒完成签到,获得积分10
1分钟前
HuLL完成签到 ,获得积分10
1分钟前
健康的电灯胆完成签到,获得积分0
1分钟前
WILD完成签到 ,获得积分10
1分钟前
稳重的安萱完成签到,获得积分10
1分钟前
zhao完成签到,获得积分10
1分钟前
可爱的茈发布了新的文献求助30
1分钟前
1分钟前
高分求助中
Introduction to Strong Mixing Conditions Volumes 1-3 500
Tip60 complex regulates eggshell formation and oviposition in the white-backed planthopper, providing effective targets for pest control 400
Optical and electric properties of monocrystalline synthetic diamond irradiated by neutrons 320
共融服務學習指南 300
Essentials of Pharmacoeconomics: Health Economics and Outcomes Research 3rd Edition. by Karen Rascati 300
Peking Blues // Liao San 300
Political Ideologies Their Origins and Impact 13 edition 240
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3800999
求助须知:如何正确求助?哪些是违规求助? 3346581
关于积分的说明 10329619
捐赠科研通 3063070
什么是DOI,文献DOI怎么找? 1681341
邀请新用户注册赠送积分活动 807491
科研通“疑难数据库(出版商)”最低求助积分说明 763726