A broadly protective antibody targeting gammaherpesvirus gB

AI Summary4 min read

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

Cryoelectron microscopyHerpes virusViral infectionScienceHumanities and Social Sciencesmultidisciplinary

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

Rent or buy this article

Prices vary by article type

from$1.95

to$39.95

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

Author information

Author notes
  1. These authors contributed equally: Cong Sun, Chu Xie, Bing-Zhen Cheng

Authors and Affiliations

  1. 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

  2. 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

Authors
  1. Cong Sun
  2. Chu Xie
  3. Bing-Zhen Cheng
  4. Zi-Ying Jiang
  5. Pei-Huang Wu
  6. Xin-Yan Fang
  7. Peng-Lin Li
  8. Xian-Shu Tian
  9. Hang Zhou
  10. Yan-Lin Yang

Visit Website