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针对猴痘的多组分 mRNA 疫苗候选物的合理开发。

Rational development of multicomponent mRNA vaccine candidates against mpox.

机构信息

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, People's Republic of China.

Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People's Republic of China.

出版信息

Emerg Microbes Infect. 2023 Dec;12(1):2192815. doi: 10.1080/22221751.2023.2192815.

Abstract

The re-emerging mpox (formerly monkeypox) virus (MPXV), a member of genus together with variola virus (VARV) and vaccinia virus (VACV), has led to public health emergency of international concern since July 2022. Inspired by the unprecedent success of coronavirus disease 2019 (COVID-19) mRNA vaccines, the development of a safe and effective mRNA vaccine against MPXV is of high priority. Based on our established lipid nanoparticle (LNP)-encapsulated mRNA vaccine platform, we rationally constructed and prepared a panel of multicomponent MPXV vaccine candidates encoding different combinations of viral antigens including M1R, E8L, A29L, A35R, and B6R. and characterization demonstrated that two immunizations of all mRNA vaccine candidates elicit a robust antibody response as well as antigen-specific Th1-biased cellular response in mice. Importantly, the penta- and tetra-component vaccine candidates AR-MPXV5 and AR-MPXV4a showed superior capability of inducing neutralizing antibodies as well as of protecting from VACV challenge in mice. Our study provides critical insights to understand the protection mechanism of MPXV infection and direct evidence supporting further clinical development of these multicomponent mRNA vaccine candidates.

摘要

重新出现的猴痘(以前称为猴痘)病毒(MPXV)是正痘病毒属的成员,与天花病毒(VARV)和牛痘病毒(VACV)一起,自 2022 年 7 月以来导致了国际关注的公共卫生紧急事件。受 2019 年冠状病毒病(COVID-19)mRNA 疫苗空前成功的启发,开发针对 MPXV 的安全有效的 mRNA 疫苗是当务之急。基于我们已建立的脂质纳米颗粒(LNP)包裹的 mRNA 疫苗平台,我们合理构建并制备了一组多成分 MPXV 疫苗候选物,这些候选物编码不同组合的病毒抗原,包括 M1R、E8L、A29L、A35R 和 B6R。和表征表明,所有 mRNA 疫苗候选物的两次免疫均可在小鼠中引起强烈的抗体反应以及抗原特异性 Th1 偏向的细胞反应。重要的是,五价和四价疫苗候选物 AR-MPXV5 和 AR-MPXV4a 显示出诱导中和抗体的优异能力,以及在小鼠中预防 VACV 挑战的能力。我们的研究提供了深入了解 MPXV 感染保护机制的重要见解,并为这些多成分 mRNA 疫苗候选物的进一步临床开发提供了直接证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b35/10071941/3e6d41a2f994/TEMI_A_2192815_F0001_OC.jpg

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