A chimeric mRNA vaccine of S-RBD with HA conferring broad protection against influenza and COVID-19 variants.

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2024-09-20 eCollection Date: 2024-09-01 DOI:10.1371/journal.ppat.1012508
Tianjiao Hao, Yulei Li, Peipei Liu, Xi Wang, Ke Xu, Wenwen Lei, Ying Li, Rong Zhang, Xiaoyan Li, Xin Zhao, Kun Xu, Xuancheng Lu, Yuhai Bi, Hao Song, Guizhen Wu, Baoli Zhu, George F Gao
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Abstract

Influenza and coronavirus disease 2019 (COVID-19) represent two respiratory diseases that have significantly impacted global health, resulting in substantial disease burden and mortality. An optimal solution would be a combined vaccine capable of addressing both diseases, thereby obviating the need for multiple vaccinations. Previously, we conceived a chimeric protein subunit vaccine targeting both influenza virus and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), utilizing the receptor binding domain of spike protein (S-RBD) and the stalk region of hemagglutinin protein (HA-stalk) components. By integrating the S-RBD from the SARS-CoV-2 Delta variant with the headless hemagglutinin (HA) from H1N1 influenza virus, we constructed stable trimeric structures that remain accessible to neutralizing antibodies. This vaccine has demonstrated its potential by conferring protection against a spectrum of strains in mouse models. In this study, we designed an mRNA vaccine candidate encoding the chimeric antigen. The resultant humoral and cellular immune responses were meticulously evaluated in mouse models. Furthermore, the protective efficacy of the vaccine was rigorously examined through challenges with either homologous or heterologous influenza viruses or SARS-CoV-2 strains. Our findings reveal that the mRNA vaccine exhibited robust immunogenicity, engendering high and sustained levels of neutralizing antibodies accompanied by robust and persistent cellular immunity. Notably, this vaccine effectively afforded complete protection to mice against H1N1 or heterosubtypic H5N8 subtypes, as well as the SARS-CoV-2 Delta and Omicron BA.2 variants. Additionally, our mRNA vaccine design can be easily adapted from Delta RBD to Omicron RBD antigens, providing protection against emerging variants. The development of two-in-one vaccine targeting both influenza and COVID-19, incorporating the mRNA platform, may provide a versatile approach to combating future pandemics.

S-RBD 与 HA 的嵌合 mRNA 疫苗,对流感和 COVID-19 变体具有广泛的保护作用。
流感和冠状病毒疾病 2019(COVID-19)是严重影响全球健康的两种呼吸道疾病,造成了巨大的疾病负担和死亡率。最佳的解决方案是能够同时预防这两种疾病的联合疫苗,从而避免了多次接种疫苗的需要。此前,我们利用尖峰蛋白的受体结合域(S-RBD)和血凝素蛋白的柄区(HA-stalk)成分,设想了一种同时针对流感病毒和严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的嵌合蛋白亚单位疫苗。通过将 SARS-CoV-2 Delta 变体的 S-RBD 与 H1N1 流感病毒的无头血凝素(HA)整合,我们构建了稳定的三聚体结构,这种结构仍可被中和抗体利用。这种疫苗在小鼠模型中对各种毒株都有保护作用,证明了它的潜力。在本研究中,我们设计了一种编码嵌合抗原的 mRNA 候选疫苗。在小鼠模型中对由此产生的体液和细胞免疫反应进行了细致的评估。此外,我们还通过对同源或异源流感病毒或 SARS-CoV-2 株的挑战,严格检验了疫苗的保护效力。我们的研究结果表明,mRNA 疫苗具有很强的免疫原性,能产生高水平且持续的中和抗体,并伴有强大而持久的细胞免疫。值得注意的是,这种疫苗能有效地为小鼠提供针对 H1N1 或异种 H5N8 亚型以及 SARS-CoV-2 Delta 和 Omicron BA.2 变体的完全保护。此外,我们的 mRNA 疫苗设计可以很容易地从 Delta RBD 抗原调整为 Omicron RBD 抗原,从而对新出现的变种提供保护。结合 mRNA 平台开发针对流感和 COVID-19 的二合一疫苗,可为应对未来的流行病提供一种多功能方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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