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基于新城疫病毒(NDV)的候选疫苗,通过鼻内免疫对抗严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎变异株

Newcastle Disease Virus (NDV)-based vaccine candidate against SARS-CoV-2 Omicron by intranasal immunization.

作者信息

Zhang Qiu-Yan, Zhang Hong-Qing, Zhang Ya-Nan, Zhang Zhe-Rui, Li Xiao-Dan, Hao Meng-Chan, Zhang Yang, Li Jia-Qi, Hu Yan-Yan, Chen Xiao-Ling, Wang Jing, Shi Yu-Jia, Deng Cheng-Lin, Chen Jian-Jun, Ye Han-Qing, Zhang Bo

机构信息

Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, China.

Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, China; University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Antiviral Res. 2023 Dec;220:105757. doi: 10.1016/j.antiviral.2023.105757. Epub 2023 Nov 19.

Abstract

Despite global vaccination efforts, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to evolve and spread globally. Currently, the development of affordable vaccine against Omicron variant of concern (VOC) is necessary. Here, we assessed the safety and immunogenicity of a SARS-CoV-2 vaccine consisting of a live Newcastle disease virus vector expressing the spike (S) protein of Omicron BA.1 administrated intranasally (IN) or intramuscularly (IM) in Golden Syrian hamster model. Immunogenicity studies showed that the prime-boost regimen elicited high antibody titers and the modified S antigen (Sm-F) could induce robust antibody response in low dosage immunization through IN route. Sera of the immunized hamsters provided effective cross-neutralizing activity against different Omicron variants, the prototype and delta strains of SARS-CoV-2. Moreover, the vaccine could provide complete immunoprotection in hamsters against the Omicron BA.1 challenge by either intranasal or intramuscular immunization. Overall, our study provides an alternative nasal vaccine against the SARS-CoV-2 Omicron variants.

摘要

尽管全球都在努力进行疫苗接种,但严重急性呼吸综合征冠状病毒2(SARS-CoV-2)仍在持续演变并在全球传播。目前,开发针对值得关注的奥密克戎变异株(VOC)的平价疫苗很有必要。在此,我们在金黄叙利亚仓鼠模型中评估了一种由表达奥密克戎BA.1刺突(S)蛋白的新城疫病毒活载体组成的SARS-CoV-2疫苗经鼻内(IN)或肌肉内(IM)接种后的安全性和免疫原性。免疫原性研究表明,初免-加强免疫方案可引发高抗体滴度,且修饰后的S抗原(Sm-F)可通过经鼻途径在低剂量免疫中诱导强烈的抗体反应。免疫仓鼠的血清对不同的奥密克戎变异株、SARS-CoV-2原型株和德尔塔株具有有效的交叉中和活性。此外,该疫苗通过鼻内或肌肉内免疫均可为仓鼠提供针对奥密克戎BA.1攻击的完全免疫保护。总体而言,我们的研究提供了一种针对SARS-CoV-2奥密克戎变异株的替代性鼻用疫苗。

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