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

IF 14.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2024-11-21 DOI:10.1038/s41467-024-54384-x
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
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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.

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针对前融合 RSV F 蛋白保守区的强效广谱中和抗体
呼吸道合胞病毒(RSV)给公共卫生带来了巨大挑战,尤其是在儿童中。虽然针对 RSV F 蛋白的中和抗体(nAbs)帕利珠单抗(palivizumab)和尼舍维单抗(nirsevimab)已被用于预防,但它们的局限性突出表明需要更有效的替代品。在本文中,我们介绍了一种名为 5B11 的强效、广谱 nAb,它对 RSV-A 和 -B 亚群都具有毫微克级的无偏中和活性。值得注意的是,与 1129(palivizumab 的小鼠前体)相比,5B11 的中和效力提高了约 20 倍;与 nirsevimab 相比,5B11 对 B18537 的中和效力提高了约 3 倍。冷冻电镜分析揭示了 5B11 的作用机制,它靶向 V 位点内的一个高度保守的表位,提供了一种具有潜在较低逃逸突变风险的有前途的策略。在雌性棉鼠模型中进行的抗病毒测试表明,低剂量(1.5 毫克/千克)服用 5B11 的预防效果与高剂量(15 毫克/千克)服用 1129 的效果相当。此外,与 nirsevimab 和 palivizumab 相比,人源化 5B11 在体内对 B18537 感染表现出更强的抗病毒活性。因此,5B11 是一种很有前景的 RSV 预防候选药物,可广泛用于预防 RSV 感染。
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来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
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