De novo design of a safe and potent respiratory syncytial virus immuno-focusing antigen

Journal: bioRxiv
Published Date:

Abstract

Respiratory syncytial virus (RSV) remains the leading cause of severe respiratory infections in infants, the elderly, and the immunocompromised. Although stabilized full-length pre-fusion (pre-F) protein vaccines are promising, enhanced respiratory disease (ERD) remains a critical safety concern. Here, we used artificial intelligence to design a de novo immuno-focused antigen that structurally preserves the RSV F head region containing critical neutralising epitopes site zero, II and V while replacing the non-neutralising stem with a computationally designed scaffold to minimise immunopathological risk. The lead candidate, aRF6, elicited robust protective immunity against RSV in mice and similar immunogenicity in non-human primates without detectable toxicity. Importantly, in stringent ERD-promoting models, aRF6 induced minimal pulmonary pathology and markedly attenuated Th2-biased cytokine responses, outperforming formalin-inactivated RSV and full-length-stabilized pre-F. The results of cryoelectron microscopy confirmed that the aRF6 structure precisely matched the computational predictions. These results demonstrated that computationally designed de novo immuno-focused antigens can yield safe and effective RSV vaccines, thereby providing a rational framework for next-generation vaccine development.

Authors

  • Kwon
  • Y.-C.; Hwang
  • W. Y.; Song
  • J.; Choe
  • J.; Ku
  • K. B.; Kim
  • H.-S.; Yoon
  • G. Y.; Kim
  • D. Y.; Choi
  • M.-R.; Kim
  • E.-J.; Lee
  • J. S.; Park
  • S.; Lee
  • S. K.; Ku
  • B.; Ahn
  • D.-G.; Kim
  • K.-D.; Kim
  • C.; Suh
  • H. N.; Lee
  • J.; Shin
  • H.-C.; Ko
  • J.

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