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mRNA 或改良安卡拉痘苗病毒疫苗对非人灵长类动物预防猴痘的效果比较。

Comparison of protection against mpox following mRNA or modified vaccinia Ankara vaccination in nonhuman primates.

机构信息

Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.

Moderna Inc., Cambridge, MA, USA.

出版信息

Cell. 2024 Oct 3;187(20):5540-5553.e10. doi: 10.1016/j.cell.2024.08.043. Epub 2024 Sep 4.

Abstract

In 2022, mpox virus (MPXV) spread worldwide, causing 99,581 mpox cases in 121 countries. Modified vaccinia Ankara (MVA) vaccine use reduced disease in at-risk populations but failed to deliver complete protection. Lag in manufacturing and distribution of MVA resulted in additional MPXV spread, with 12,000 reported cases in 2023 and an additional outbreak in Central Africa of clade I virus. These outbreaks highlight the threat of zoonotic spillover by Orthopoxviruses. mRNA-1769, an mRNA-lipid nanoparticle (LNP) vaccine expressing MPXV surface proteins, was tested in a lethal MPXV primate model. Similar to MVA, mRNA-1769 conferred protection against challenge and further mitigated symptoms and disease duration. Antibody profiling revealed a collaborative role between neutralizing and Fc-functional extracellular virion (EV)-specific antibodies in viral restriction and ospinophagocytic and cytotoxic antibody functions in protection against lesions. mRNA-1769 enhanced viral control and disease attenuation compared with MVA, highlighting the potential for mRNA vaccines to mitigate future pandemic threats.

摘要

2022 年,猴痘病毒(MPXV)在全球范围内传播,导致 121 个国家的 99581 例猴痘病例。改良安卡拉牛痘病毒(MVA)疫苗的使用减少了高危人群的疾病,但未能提供完全的保护。MVA 的制造和分发延迟导致了更多的 MPXV 传播,2023 年报告了 12000 例病例,中非再次爆发 I 型病毒。这些疫情突显了正痘病毒通过动物传播的威胁。表达 MPXV 表面蛋白的 mRNA-1769 脂质纳米颗粒(LNP)疫苗在致命的 MPXV 灵长类动物模型中进行了测试。与 MVA 相似,mRNA-1769 提供了针对挑战的保护,并进一步减轻了症状和疾病持续时间。抗体分析揭示了中和和 Fc 功能细胞外病毒(EV)特异性抗体在病毒限制和吞噬和细胞毒性抗体功能中的协同作用,以保护免受损伤。与 MVA 相比,mRNA-1769 增强了病毒控制和疾病缓解,突出了 mRNA 疫苗减轻未来大流行威胁的潜力。

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