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一种针对 RSV F 蛋白前融合保守区域的强效广谱中和抗体。

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

机构信息

State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health, Xiamen University, Xiamen, P. R. China.

National Institute of Diagnostics and Vaccine Development in Infectious Diseases, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Xiamen University, Xiamen, P. R. China.

出版信息

Nat Commun. 2024 Nov 21;15(1):10085. doi: 10.1038/s41467-024-54384-x.

DOI:10.1038/s41467-024-54384-x
PMID:39572535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11582626/
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.

摘要

呼吸道合胞病毒(RSV)对公共健康构成重大挑战,特别是对儿童而言。虽然帕利珠单抗和奈昔单抗(靶向 RSV F 蛋白的中和抗体)已被用于预防,但它们的局限性突显了需要更有效的替代品。在此,我们介绍了一种强效且广谱的中和抗体,命名为 5B11,它对 RSV-A 和 -B 亚群均表现出纳克级别的无偏中和活性。值得注意的是,与 1129 相比,5B11 的中和效力提高了约 20 倍,与 nirsevimab 相比,对 B18537 的中和效力提高了约 3 倍。冷冻电子显微镜分析揭示了 5B11 通过靶向结构域 V 内的一个高度保守表位发挥作用的机制,提供了一种具有潜在较低逃逸突变风险的有前途的策略。在雌性棉鼠模型中的抗病毒测试表明,低剂量(1.5mg/kg)的 5B11 给药可达到与高剂量(15mg/kg)的 1129 相当的预防效果。此外,人源化 5B11 对 B18537 感染的体内抗病毒活性优于 nirsevimab 和 palivizumab。因此,5B11 是一种有前途的 RSV 预防性候选药物,可广泛预防 RSV 感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d8a/11582626/b478383d587c/41467_2024_54384_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d8a/11582626/b478383d587c/41467_2024_54384_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d8a/11582626/36fdbbbe7080/41467_2024_54384_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d8a/11582626/61154563d92f/41467_2024_54384_Fig2_HTML.jpg
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