Nature Communications (Nov 2024)

A potent broad-spectrum neutralizing antibody targeting a conserved region of the prefusion RSV F protein

  • Yongpeng Sun,
  • Liqin Liu,
  • Hongsheng Qiang,
  • Hui Sun,
  • Yichao Jiang,
  • Luo Ren,
  • Zemin Jiang,
  • Siyu Lei,
  • Li Chen,
  • Yizhen Wang,
  • Xue Lin,
  • Guosong Wang,
  • Yang Huang,
  • Yuhao Fu,
  • Yujin Shi,
  • Xiuting Chen,
  • Hai Yu,
  • Shaowei Li,
  • Wenxin Luo,
  • Enmei Liu,
  • Qingbing Zheng,
  • Zizheng Zheng,
  • Ningshao Xia

DOI
https://doi.org/10.1038/s41467-024-54384-x
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract Respiratory syncytial virus (RSV) poses a significant public health challenge, especially among children. Although palivizumab and nirsevimab, neutralizing antibodies (nAbs) targeting the RSV F protein, have been used for prophylaxis, their limitations underscore the need for more effective alternatives. Herein, we present a potent and broad nAb, named 5B11, which exhibits nanogram level of unbiased neutralizing activities against both RSV-A and -B subgroups. Notably, 5B11 shows a ~20-fold increase in neutralizing efficacy compared to 1129 (the murine precursor of palivizumab) and approximately a 3-fold increase in neutralizing efficacy against B18537 in comparison to nirsevimab. Cryo-electron microscopy analysis reveals 5B11’s mechanism of action by targeting a highly conserved epitope within site V, offering a promising strategy with potentially lower risk of escape mutants. Antiviral testing in a female cotton rat model demonstrated that low-dose (1.5 mg/kg) administration of 5B11 achieved comparable prophylactic efficacy to that achieved by high-dose (15 mg/kg) of 1129. Furthermore, the humanized 5B11 showed a superior in vivo antiviral activity against B18537 infection compared to nirsevimab and palivizumab. Therefore, 5B11 is a promising RSV prophylactic candidate applicable to broad prevention of RSV infection.