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SARS-CoV-2 抗原决定簇的保守性与进化:免疫逃逸和疫苗设计的新视角。

Conservation and Evolution of Antigenic Determinants of SARS-CoV-2: An Insight for Immune Escape and Vaccine Design.

机构信息

Department of Food and Nutrition, College of BioNano Technology, Gachon University, Seongnam-si, South Korea.

Institute for Aging and Clinical Nutrition Research, Gachon University, Seongnam-si, South Korea.

出版信息

Front Immunol. 2022 Apr 4;13:832106. doi: 10.3389/fimmu.2022.832106. eCollection 2022.

Abstract

Coronavirus disease 2019 (COVID-19) is the most devastating pandemic of the century, which is still far from over. The remarkable success of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines is the working hope, but the evolving variants are the huge concern that can turn the tide. Potential immune escape mutations (PIEMs) in the past and circulating variants were not studied at large scale (all available data). Hence, the conservation of antigenic determinants (epitopes) was analyzed in all available sequences of SARS-CoV-2 according to time (months), proteins, hosts, and variants. Numerous highly conserved B- and T-cell epitopes were identified in 24 proteins of SARS-CoV-2. A decrease in the conservation of epitopes with time was observed in almost all proteins, which was more rapid in neutralizing epitopes. Delta variant still has the highest PIEM in the circulating strains, which pose threat to the effectiveness of current vaccines. The inclusion of identified, highly conserved, and important epitopes in subunit vaccines can increase vaccine effectiveness against evolving variants. Trends in the conservation of epitopes in different proteins, hosts, and variants with time may also help to inspire the counter measure against the current pandemic.

摘要

新型冠状病毒病(COVID-19)是本世纪最具破坏性的大流行病,目前仍远未结束。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗的显著成功是工作的希望,但不断演变的变体是巨大的关注点,可能会改变局面。过去的潜在免疫逃逸突变(PIEM)和循环变体没有进行大规模研究(所有可用数据)。因此,根据时间(月)、蛋白质、宿主和变体,对 SARS-CoV-2 的所有可用序列中的抗原决定簇(表位)进行了保守性分析。在 SARS-CoV-2 的 24 种蛋白质中鉴定出了许多高度保守的 B 细胞和 T 细胞表位。几乎所有蛋白质中的表位保守性随时间的推移而降低,中和表位的降低速度更快。Delta 变体在流行株中仍然具有最高的 PIEM,这对当前疫苗的有效性构成威胁。在亚单位疫苗中加入已鉴定的、高度保守的和重要的表位可以提高疫苗对不断演变的变体的有效性。不同蛋白质、宿主和变体随时间的表位保守性趋势也可能有助于激发针对当前大流行的对策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a743/9014086/198c62c7c16e/fimmu-13-832106-g001.jpg

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