A cavity-reduced prefusion RSV F bivalent vaccine elicits durable and protective immunity

Authors:

Abstract
Respiratory syncytial virus (RSV) remains a major cause of severe respiratory disease, and stabilization of the prefusion (preF) conformation of the F glycoprotein is central for vaccine development. Here, we report a structure-guided engineering strategy that enhances preF stability by reducing the hydrophobic cavity within the trimeric F protein. Targeted modifications at metastability-associated sites generated RVF-88, a disulfide-free stabilized preF immunogen that preserves key neutralizing epitopes, including antigenic site Ø, while exhibiting improved structural integrity and long-term storage stability. Formulated as an unadjuvanted bivalent vaccine, RVF-88 elicited potent neutralizing antibody responses and durable immune protection lasting up to 5 months in mice. Vaccination also protected both mice and cotton rats against RSV challenge. Structural analyses confirmed the intended cavity-reduction design, revealing a reduced apical hydrophobic cavity volume and surface area while maintaining the prefusion architecture. Together, these findings establish hydrophobic cavity reduction as a rational strategy for stabilizing prefusion RSV F and provide a promising next-generation vaccine candidate with improved stability and immunogenicity for further clinical development.
Funding Information
  • Guangzhou National Laboratory (YW-JCZD0105)
  • Guangzhou National Laboratory (GZNL2025C01020)
  • Guangzhou National Laboratory (GZNL2023A01007)
  • State Key Laboratory of Respiratory Disease (SKLRD-Z-202512)
  • Basic and Applied Basic Research Foundation of Guangdong Province (2025A1515011053)
  • Guangzhou Municipal Science and Technology Program key projects (2023QN10Y428)
  • National Natural Science Foundation of China (32100142)
  • State Key Laboratory of Medicinal Chemical Biology (2025010)
  • State Key Laboratory of Medicinal Chemical Biology (2025013)

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