Kuroda Makoto, Halfmann Peter J, Uraki Ryuta, Yamayoshi Seiya, Kim Taksoo, Armbrust Tammy A, Spyra Sam, Dahn Randall, Babujee Lavanya, Kawaoka Yoshihiro
Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, 53711, USA.
Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan.
Nat Commun. 2025 May 14;16(1):4453. doi: 10.1038/s41467-025-59533-4.
To address the need for broadly protective SARS-CoV-2 vaccines, we developed an attenuated a SARS-CoV-2 vaccine virus that lacks the open reading frames of two viral structural proteins: the envelope (E) and membrane (M) proteins. This vaccine virus (ΔEM) replicates in a cell line stably expressing E and M but not in wild-type cells. Vaccination with ΔEM elicits a CD8 T-cell response against the viral spike and nucleocapsid proteins. Two vaccinations with ΔEM provide better protection of the lower respiratory tissues than a single dose against the Delta and Omicron XBB variants in hamsters. Moreover, ΔEM is effective as a booster in hamsters previously vaccinated with an mRNA-based vaccine, providing higher levels of protection in both respiratory tissues compared to the mRNA vaccine booster. Collectively, our data demonstrate the feasibility of a SARS-CoV-2 ΔEM vaccine candidate virus as a vaccine platform.
为满足对具有广泛保护作用的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗的需求,我们开发了一种减毒的SARS-CoV-2疫苗病毒,该病毒缺乏两种病毒结构蛋白的开放阅读框:包膜(E)蛋白和膜(M)蛋白。这种疫苗病毒(ΔEM)在稳定表达E和M的细胞系中复制,但不在野生型细胞中复制。用ΔEM疫苗接种可引发针对病毒刺突蛋白和核衣壳蛋白的CD8 T细胞反应。在仓鼠中,用ΔEM进行两次接种比单次接种能更好地保护下呼吸道组织免受德尔塔和奥密克戎XBB变体的侵害。此外,ΔEM作为先前接种过基于mRNA疫苗的仓鼠的加强针是有效的,与mRNA疫苗加强针相比,在两个呼吸道组织中都提供了更高水平的保护。总体而言,我们的数据证明了SARS-CoV-2 ΔEM候选疫苗病毒作为疫苗平台的可行性。