候选病毒样颗粒疫苗抗SARS-CoV-2感染的免疫原性

Access microbiology Pub Date : 2025-02-17 eCollection Date: 2025-01-01 DOI:10.1099/acmi.0.000925.v3
Hai Trong Nguyen, Ravendra Garg, Andrea Kroeker, Volker Gerdts, Darryl Falzarano, Qiang Liu
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引用次数: 0

摘要

严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)继续演变,可能导致令人担忧的变体,这些变体可能变得更具传染性、抵抗治疗、逃避宿主免疫并降低现有疫苗的有效性。由于疫苗接种仍然是对抗这种病毒的最有效策略,因此仍需要改进疫苗。我们利用杆状病毒BacMam表达平台制备了两种SARS-CoV-2病毒样颗粒(VLPs),并在小鼠中检测了它们的免疫原性。VLP1含有武汉株的刺突蛋白,而VLP2含有一种Omicron变体的刺突蛋白。与对照组相比,用VLP1免疫和用VLP2增强的小鼠在血清中产生了明显更高的抗体,以及更多的IFN-γ分泌细胞。此外,两种VLPs都诱导了针对武汉和Omicron变体的病毒中和抗体。总之,VLPs具有开发安全有效的SARS-CoV-2变体疫苗的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity of virus-like particle vaccine candidates against SARS-CoV-2 infection.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to evolve, potentially leading to variants of concern that could become more transmissible, resist treatment, evade host immunity and reduce the effectiveness of currently available vaccines. Improved vaccines are still required as vaccination remains the most effective strategy against this virus. We have produced two SARS-CoV-2 virus-like particles (VLPs) using a baculovirus BacMam expression platform and examined their immunogenicity in mice. VLP1 contains the spike protein from the Wuhan strain, whereas VLP2 contains that of an Omicron variant. Mice immunized with VLP1 and boosted with VLP2 developed significantly higher antibodies in the sera, as well as higher numbers of IFN-γ secreting cells than the control group. Furthermore, both VLPs induced virus-neutralizing antibodies against Wuhan and Omicron variants. In conclusion, VLPs have the potential for the development of a safe and effective vaccine against SARS-CoV-2 variants.

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