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SARS-CoV-2 刺突蛋白:疫苗的最佳免疫靶标。

SARS-CoV-2 SPIKE PROTEIN: an optimal immunological target for vaccines.

机构信息

Takis s.r.l, Via di Castel Romano 100, 00128, Rome, Italy.

Evvivax s.r.l, Via di Castel Romano, 100, 00128, Rome, Italy.

出版信息

J Transl Med. 2020 Jun 3;18(1):222. doi: 10.1186/s12967-020-02392-y.

DOI:10.1186/s12967-020-02392-y
PMID:32493510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7268185/
Abstract

COVID-19 has rapidly spread all over the world, progressing into a pandemic. This situation has urgently impelled many companies and public research institutes to concentrate their efforts on research for effective therapeutics. Here, we outline the strategies and targets currently adopted in developing a vaccine against SARS-CoV-2. Based on previous evidence and experience with SARS and MERS, the primary focus has been the Spike protein, considered as the ideal target for COVID-19 immunotherapies.

摘要

COVID-19 已迅速在全球蔓延,演变成大流行。这种情况紧急促使许多公司和公共研究机构集中精力研究有效的治疗方法。在这里,我们概述了目前开发针对 SARS-CoV-2 疫苗所采用的策略和靶标。基于以前对 SARS 和 MERS 的证据和经验,主要关注点是 Spike 蛋白,它被认为是 COVID-19 免疫疗法的理想靶标。

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本文引用的文献

1
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Cell Mol Immunol. 2020 Jun;17(6):613-620. doi: 10.1038/s41423-020-0400-4. Epub 2020 Mar 19.
2
Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein.严重急性呼吸系统综合征冠状病毒 2 刺突糖蛋白的结构、功能和抗原性。
Cell. 2020 Apr 16;181(2):281-292.e6. doi: 10.1016/j.cell.2020.02.058. Epub 2020 Mar 9.
3
Is COVID-19 receiving ADE from other coronaviruses?新冠病毒是否会从其他冠状病毒中获得增强效应?
Microbes Infect. 2020 Mar;22(2):72-73. doi: 10.1016/j.micinf.2020.02.006. Epub 2020 Feb 22.
4
Evaluation of Antibody-Dependent Enhancement of SARS-CoV Infection in Rhesus Macaques Immunized with an Inactivated SARS-CoV Vaccine.用灭活SARS-CoV疫苗免疫的恒河猴中SARS-CoV感染的抗体依赖性增强作用的评估
Virol Sin. 2018 Apr;33(2):201-204. doi: 10.1007/s12250-018-0009-2. Epub 2018 Mar 14.
5
Prophylactic and postexposure efficacy of a potent human monoclonal antibody against MERS coronavirus.一种强效人源单克隆抗体对中东呼吸综合征冠状病毒的预防及暴露后疗效
Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):10473-8. doi: 10.1073/pnas.1510199112. Epub 2015 Jul 27.
6
Antibody-dependent SARS coronavirus infection is mediated by antibodies against spike proteins.抗体依赖性 SARS 冠状病毒感染是由针对刺突蛋白的抗体介导的。
Biochem Biophys Res Commun. 2014 Aug 22;451(2):208-14. doi: 10.1016/j.bbrc.2014.07.090. Epub 2014 Jul 26.
7
Antibody-dependent infection of human macrophages by severe acute respiratory syndrome coronavirus.严重急性呼吸综合征冠状病毒通过抗体依赖性感染人巨噬细胞。
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8
Immunization with SARS coronavirus vaccines leads to pulmonary immunopathology on challenge with the SARS virus.接种 SARS 冠状病毒疫苗会导致在 SARS 病毒攻击时肺部免疫病理学发生。
PLoS One. 2012;7(4):e35421. doi: 10.1371/journal.pone.0035421. Epub 2012 Apr 20.
9
An efficient method to make human monoclonal antibodies from memory B cells: potent neutralization of SARS coronavirus.一种从记忆B细胞制备人单克隆抗体的有效方法:对严重急性呼吸综合征冠状病毒的有效中和作用
Nat Med. 2004 Aug;10(8):871-5. doi: 10.1038/nm1080. Epub 2004 Jul 11.
10
Contributions of the structural proteins of severe acute respiratory syndrome coronavirus to protective immunity.严重急性呼吸综合征冠状病毒结构蛋白对保护性免疫的贡献。
Proc Natl Acad Sci U S A. 2004 Jun 29;101(26):9804-9. doi: 10.1073/pnas.0403492101. Epub 2004 Jun 21.