Department of Laboratory Medicine, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230031, China; Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Antiviral Res. 2024 Oct;230:105974. doi: 10.1016/j.antiviral.2024.105974. Epub 2024 Jul 31.
The outbreak of 2022 monkeypox virus (MPXV) infection in nonendemic regions is a global public health concern. A highly effective and safe MPXV vaccine that is available to the general public is urgently needed to control the mpox pandemic. Here, we developed a multivalent mRNA vaccine candidate, MPXV-1103, which expresses the full-length B6, A35, A29 and M1 proteins with three flexible linkers (GS) in a single sequence. Compared with the monovalent MPXV mRNA vaccine candidates or the quadrivalent mRNA vaccine from mixtures of the four monovalent MPXV mRNA vaccines, MPXV-1103 elicits a robust humoral response and an MPXV-specific T-cell response and protects mice from lethal vaccinia virus (VACV) challenge, with no live virus detected in the nasal or lungs even at dosages as low as 1 μg. Furthermore, analysis of complete blood counts and photomicrographs of tissue from the main organs of mice vaccinated with MPXV-1103 at doses of 5 μg and 20 μg revealed that two doses of MPXV-1103 did not cause any observable pathological changes in the mice. Collectively, our results suggest that MPXV-1103, with features of high efficacy, safety and a simplified manufacturing process, is a promising vaccine candidate for defending against MPXV infection.
2022 年猴痘病毒(MPXV)在非流行地区的爆发是全球公共卫生关注的问题。急需一种可广泛使用的、高效且安全的 MPXV 疫苗来控制猴痘大流行。在这里,我们开发了一种多价 mRNA 疫苗候选物 MPXV-1103,它在单个序列中用三个柔性接头(GS)表达全长 B6、A35、A29 和 M1 蛋白。与单价 MPXV mRNA 疫苗候选物或由四种单价 MPXV mRNA 疫苗混合物制成的四价 mRNA 疫苗相比,MPXV-1103 可引发强大的体液免疫和 MPXV 特异性 T 细胞应答,并可保护小鼠免受致死性牛痘病毒(VACV)的攻击,即使在低至 1μg 的剂量下,鼻腔或肺部也未检测到活病毒。此外,对用 5μg 和 20μg 剂量的 MPXV-1103 接种的小鼠的主要器官的完整血球计数和组织照片进行分析表明,两剂 MPXV-1103 不会引起小鼠任何可观察到的病理变化。总的来说,我们的结果表明,MPXV-1103 具有高效、安全和简化的制造工艺的特点,是一种有前途的抵御 MPXV 感染的疫苗候选物。