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严重急性呼吸综合征冠状病毒2的基因组变异、溯源及疫苗研发:一项系统综述

Genomic variation, origin tracing, and vaccine development of SARS-CoV-2: A systematic review.

作者信息

Li Tianbao, Huang Tao, Guo Cheng, Wang Ailan, Shi Xiaoli, Mo Xiaofei, Lu Qingqing, Sun Jing, Hui Tingting, Tian Geng, Wang Leyi, Yang Jialiang

机构信息

Genetic Testing Center, Academician Workstation, Changsha Medical University, Changsha 410219, China.

Geneis (Beijing) Co., Ltd, Beijing 100102, China.

出版信息

Innovation (Camb). 2021 May 28;2(2):100116. doi: 10.1016/j.xinn.2021.100116. Epub 2021 May 11.

DOI:10.1016/j.xinn.2021.100116
PMID:33997827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8110321/
Abstract

COVID-19 has spread globally to over 200 countries with more than 40 million confirmed cases and one million deaths as of November 1, 2020. The SARS-CoV-2 virus, leading to COVID-19, shows extremely high rates of infectivity and replication, and can result in pneumonia, acute respiratory distress, or even mortality. SARS-CoV-2 has been found to continue to rapidly evolve, with several genomic variants emerging in different regions throughout the world. In addition, despite intensive study of the spike protein, its origin, and molecular mechanisms in mediating host invasion are still only partially resolved. Finally, the repertoire of drugs for COVID-19 treatment is still limited, with several candidates still under clinical trial and no effective therapeutic yet reported. Although vaccines based on either DNA/mRNA or protein have been deployed, their efficacy against emerging variants requires ongoing study, with multivalent vaccines supplanting the first-generation vaccines due to their low efficacy against new strains. Here, we provide a systematic review of studies on the epidemiology, immunological pathogenesis, molecular mechanisms, and structural biology, as well as approaches for drug or vaccine development for SARS-CoV-2.

摘要

截至2020年11月1日,新冠病毒病已在全球蔓延至200多个国家,确诊病例超过4000万例,死亡人数达100万。导致新冠病毒病的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)显示出极高的感染率和复制率,并可导致肺炎、急性呼吸窘迫甚至死亡。已发现SARS-CoV-2在持续快速进化,世界各地不同地区出现了几种基因组变体。此外,尽管对刺突蛋白进行了深入研究,但其起源以及介导宿主入侵的分子机制仍仅得到部分解决。最后,用于治疗新冠病毒病的药物种类仍然有限,几种候选药物仍在临床试验中,尚未报告有有效的治疗方法。尽管基于DNA/信使核糖核酸(mRNA)或蛋白质的疫苗已经投入使用,但其对新出现变体的有效性仍需持续研究,由于第一代疫苗对新毒株的效力较低,多价疫苗正在取代它们。在此,我们对有关SARS-CoV-2的流行病学、免疫发病机制、分子机制和结构生物学以及药物或疫苗开发方法的研究进行了系统综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cc/8454661/3f45805f6bf1/gr4.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cc/8454661/3f45805f6bf1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cc/8454661/3c5997c6aaab/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cc/8454661/a5a837984892/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76cc/8454661/76b735c01086/gr2.jpg
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