COVID-19疫苗的演变及其后续。

IF 2.9 Q2 NEUROSCIENCES Neuroscience Insights Pub Date : 2023-01-01 DOI:10.1177/26331055231180543
Yardley Brice, Larry Morgan, Maaida Kirmani, Maha Kirmani, Mercy C Udeh
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引用次数: 1

摘要

2019年12月,中国首次报告了一种新的严重急性呼吸系统综合征冠状病毒-2 (SARS CoV-2)。它将迅速传播并成为COVID-19大流行。由SARS - CoV-2引起的疾病属于临床范围,从无症状、轻微到严重的呼吸道症状、急性呼吸窘迫综合征和死亡。这导致了显著的发病率和死亡率,进一步影响了有严重并发症的高危人群。因此,全世界齐心协力应对COVID-19的诊断、治疗和预防挑战,推动了医学的快速进步。一些缓解方法,如戴口罩、保持社交距离和勤洗手,有助于减缓SARS-CoV-2的传播。由抗病毒药物和单克隆抗体组成的有效治疗方法及其用于预防,有助于COVID-19的管理。来自不同平台(mRNA、病毒载体、蛋白基和灭活疫苗)的疫苗有助于降低发病率、严重程度,总体上降低住院率和死亡率。本文旨在综述新型mRNA疫苗(Moderna + Pfizer/BioNTech)、病毒载体(Janssen& Johnson)和蛋白基(Novavax)、它们的副作用以及它们作为增强剂的用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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COVID-19 Vaccine Evolution and Beyond.

In December 2019, a new severe acute respiratory syndrome coronavirus-2 (SARS CoV-2) was first reported in China. It would quickly spread and emerge as a COVID-19 pandemic. The illness caused by SARS CoV-2 would fall on a clinical spectrum ranging from asymptomatic, mild to severe respiratory symptoms, ARDS, and death. This led to significant morbidity and mortality further impacting at-risk populations with severe complications. Thus, a concerted worldwide effort to meet the challenges of diagnosing, treating, and preventing COVID-19 led to rapid advances in medicine. Some mitigating methods of masking, social distancing, and frequent handwashing, helped to slow the spread of SARS-CoV-2. Effective therapeutics consisting of antivirals and monoclonal antibodies, plus their use for prophylaxis, contributed to the management of COVID-19. The vaccines from various platforms (mRNA, viral vectors, protein base, and inactivated) contributed to decreased incidence, severity, and overall decreased hospitalizations and mortality. This article aims to review the novel mRNA vaccines (Moderna + Pfizer/BioNTech), viral vector (Janssen& Johnson), and protein base (Novavax), their side effects, and their use as boosters.

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来源期刊
Neuroscience Insights
Neuroscience Insights Neuroscience-Neuroscience (all)
CiteScore
6.10
自引率
0.00%
发文量
24
审稿时长
9 weeks
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