生物
牛痘
爆发
病毒学
接种疫苗
病毒
抗体
大流行
疾病
免疫学
传染病(医学专业)
遗传学
2019年冠状病毒病(COVID-19)
基因
医学
重组DNA
病理
作者
Eric M. Mucker,Alec W. Freyn,Sandra L. Bixler,Deniz Cizmeci,Caroline Atyeo,Patricia L. Earl,Harini Natarajan,Genesis Santos,Tiffany R. Frey,R. H. Levin,Anusha Meni,Guha Asthagiri Arunkumar,Daniel Stadlbauer,Patricia A. Jorquera,Hamilton Bennett,Jeff Johnson,Kath Hardcastle,Jeffrey L. Americo,Catherine A. Cotter,Jeffrey W. Koehler
出处
期刊:Cell
[Cell Press]
日期:2024-09-04
卷期号:187 (20): 5540-5553.e10
被引量:76
标识
DOI:10.1016/j.cell.2024.08.043
摘要
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.
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