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新冠疫苗接种时代的新型冠状病毒2019近期展望及影响

Recent SARS-CoV-2 Outlook and Implications in a COVID-19 Vaccination Era.

作者信息

Ehianeta Teddy, Mzee Said Abdulrahman Salim, Adebisi Muslimat Kehinde, Ehianeta Oluwayemisi

机构信息

Institute of Biological Chemistry, "Academia Sinica," Taipei, Taiwan, China.

Jiangbing Hospital, Affiliated to Jiangsu University, Zhenjiang, Jiangsu, China.

出版信息

Infect Microbes Dis. 2021 Aug 13;3(3):125-133. doi: 10.1097/IM9.0000000000000072. eCollection 2021 Sep.

Abstract

While repurposed drugs came in handy earlier in the wake of the coronavirus disease 2019 (COVID-19) pandemic, vaccination has been considered a more sustainable approach. The recent spikes have been linked to "double," "triple," and even multi-mutant variants, thus renewing calls for deeper structural and functional insights of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as a lead to rationale design of therapeutics, vaccines, and point-of-care diagnostics. There is a repertoire of findings from the earliest SARS-CoV-2 molecular mimicry to evade host immunity cum host immune responses to the role of the viral glycocalyx in modulating the susceptibility and severity of infection through attraction and repulsive interactions. Recently, molecular studies of some viral components that aid infection in the face of vaccination seem unending. In addition, the wave of infections and the attendant case fatality ratios have necessitated the need for emergency use authorizations for COVID-19 vaccines and in vitro diagnostics. This review provides key updates of SARS-CoV-2, current antigenic and formulation strategies, with emergency use authorizations considerations for future vaccine candidates and diagnostics. We also premise that despite the difficulty in modeling and analyzing glycans, understanding and exploiting their roles in the SARS-CoV-2 architecture is fundamental to glycan-based COVID-19 vaccines devoid of inconsistent clinical outcomes.

摘要

在2019冠状病毒病(COVID-19)大流行早期,重新利用的药物派上了用场,但疫苗接种被认为是一种更具可持续性的方法。最近的疫情高峰与“双突变”“三突变”甚至多突变变种有关,因此再次呼吁对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)进行更深入的结构和功能研究,以便为治疗药物、疫苗和即时诊断的合理设计提供依据。从最早的SARS-CoV-2分子模拟以逃避宿主免疫到宿主免疫反应,再到病毒糖萼通过吸引和排斥相互作用在调节感染易感性和严重性方面的作用,已有一系列研究结果。最近,针对一些在接种疫苗后仍有助于感染的病毒成分的分子研究似乎无穷无尽。此外,感染浪潮和随之而来的病死率使得有必要对COVID-19疫苗和体外诊断进行紧急使用授权。本综述提供了SARS-CoV-2的关键更新、当前的抗原和配方策略,以及对未来候选疫苗和诊断方法的紧急使用授权考量。我们还提出,尽管对聚糖进行建模和分析存在困难,但了解和利用它们在SARS-CoV-2结构中的作用对于避免临床结果不一致的基于聚糖的COVID-19疫苗至关重要。

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