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基于细胞的巨细胞病毒 COVID-19 疫苗在小鼠中诱导针对 SARS-CoV-2 奥密克戎变异株(BA.2)的中和抗体。

Cytomegalovirus-vectored COVID-19 vaccines elicit neutralizing antibodies against the SARS-CoV-2 Omicron variant (BA.2) in mice.

机构信息

School of Biological Sciences and Biotechnology, Minnan Normal University , Zhangzhou, Fujian, China.

Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers-New Jersey Medical School , Newark, New Jersey, USA.

出版信息

Microbiol Spectr. 2023 Dec 12;11(6):e0246323. doi: 10.1128/spectrum.02463-23. Epub 2023 Nov 16.

Abstract

Cytomegalovirus (CMV) has been used as a novel viral vector for vaccine development and gene therapy. Coronavirus disease 2019 is an infectious disease caused by the SARS-CoV-2 virus, which is highly mutable and is still circulating globally. The study showed that the CMV viral vector caused transient systemic infection and induced robust transgene expression . CMV vectors expressing different SARS-CoV-2 proteins were immunogenic and could elicit neutralizing antibodies against a highly mutated Omicron variant (BA.2). The expression level of receptor-binding domain (RBD) protein was higher than that of full-length S protein using CMV as a vaccine vector, and CMV vector expression RBD protein elicited higher RBD-binding and neutralizing antibodies. Moreover, the study showed that CMV-vectored vaccines would not cause unexpected viral transmission, and pre-existing immunity might impair the immunogenicity of subsequent CMV-vectored vaccines. These works provide meaningful insights for the development of a CMV-based vector vaccine platform and the prevention and control strategies for SARS-CoV-2 infection.

摘要

巨细胞病毒(CMV)已被用作新型病毒载体用于疫苗开发和基因治疗。COVID-19 是一种由 SARS-CoV-2 病毒引起的传染病,该病毒高度易变且仍在全球范围内传播。研究表明,CMV 病毒载体引起短暂的全身感染,并诱导强烈的转基因表达。表达不同 SARS-CoV-2 蛋白的 CMV 载体具有免疫原性,并能针对高度突变的奥密克戎变异体(BA.2)产生中和抗体。使用 CMV 作为疫苗载体时,受体结合域(RBD)蛋白的表达水平高于全长 S 蛋白,CMV 载体表达的 RBD 蛋白引发更高的 RBD 结合和中和抗体。此外,该研究表明,CMV 载体疫苗不会引起意外的病毒传播,并且预先存在的免疫可能会损害后续 CMV 载体疫苗的免疫原性。这些工作为开发基于 CMV 的载体疫苗平台以及预防和控制 SARS-CoV-2 感染的策略提供了有意义的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc70/10883801/a56b47e36d03/spectrum.02463-23.f001.jpg

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