A broadly protective antibody targeting gammaherpesvirus gB
TL;DR
A study identifies antibody Fab5, which targets a conserved epitope on gammaherpesvirus gB, enabling broad cross-genus neutralization and protection in animal models. This finding advances potential for universal vaccines against gammaherpesviruses.
Key Takeaways
- •Antibody Fab5 targets a conserved and vulnerable epitope on gammaherpesvirus gB, enabling broad cross-genus neutralization.
- •Fab5 provides effective protection against gammaherpesvirus infections in immune-competent mice, non-human primates, and humanized mice.
- •Cryo-EM structures reveal the epitope is antigenically exposed in both pre- and post-fusion states of gB.
- •This research offers insights into common herpesvirus infection mechanisms and facilitates development of broad-spectrum vaccines.
Tags
Abstract
Gammaherpesvirus is a subfamily of herpesvirus, distinct phylogenetically from alpha- and betaherpesvirus and featured by its oncogenic subtypes, including Epstein-Barr virus and Kaposi’s sarcoma-associated herpesvirus1. It broadly infects humans and other vertebrate animals and causes various diseases and malignancies2,3. However, no specific antiviral agents are available for each type or the whole family. gB is the common fusion protein vital for herpesvirus infection and an ideal target for broad vaccine development, while the lack of basis for gB as a universal antigen hinders such effort4. Here, we report the molecular basis for broad gB binding and cross-genus virus neutralization by an antibody Fab5 for the first time. This antibody confers effective protection against authentic virus challenges in immune-competent mice, non-human primates, and humanized mice with murine, rhesus, and human gammaherpesvirus. Cryo-EM structures revealed that Fab5 targeted a conservative and vulnerable epitope of gammaherpesvirus gB and antigenically exposed across pre- or post-fusion status. This finding not only demonstrates Fab5 as cross-genus antibody broadly reactive against gammaherpesvirus infection and pathogenesis progression, but offers insights into potential common mechanisms for herpesvirus infection and facilitates the development of broad-spectrum vaccines against the gammaherpesvirus.
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$32.99 / 30 days
cancel any time
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others

A broadly neutralizing antibody confers cross-genus protection against alphaherpesviruses by inhibiting gB-mediated membrane fusion

Cross-herpesvirus immunity of the cytomegalovirus gB/MF59 vaccine response

Barrier-to-autointegration factor 1 promotes gammaherpesvirus reactivation from latency
Author information
These authors contributed equally: Cong Sun, Chu Xie, Bing-Zhen Cheng
Authors and Affiliations
State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou, China
Cong Sun, Chu Xie, Zi-Ying Jiang, Pei-Huang Wu, Peng-Lin Li, Xian-Shu Tian, Hang Zhou, Yan-Lin Yang, Jing Wang & Mu-Sheng Zeng
Cryo-electron Microscopy Center and Department of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China
Bing-Zhen Cheng, Xin-Yan Fang, Sen-Fang Sui & Zheng Liu
- Cong Sun
Search author on:PubMed Google Scholar
- Chu Xie
Search author on:PubMed Google Scholar
- Bing-Zhen Cheng
Search author on:PubMed Google Scholar
- Zi-Ying Jiang
Search author on:PubMed Google Scholar
- Pei-Huang Wu
Search author on:PubMed Google Scholar
- Xin-Yan Fang
Search author on:PubMed Google Scholar
- Peng-Lin Li
Search author on:PubMed Google Scholar
- Xian-Shu Tian
Search author on:PubMed Google Scholar
- Hang Zhou
Search author on:PubMed Google Scholar
- Yan-Lin Yang
Search author on:PubMed