疫苗对SARS-CoV-2感染的有效性、安全性和免疫反应

M. Pal, K. Gutama
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引用次数: 3

摘要

自宣布全球COVID-19大流行以来,寻找疫苗一直是重中之重。目前,针对SARS-CoV-2的疫苗有基于mrna的疫苗、基于腺病毒的疫苗、灭活病毒疫苗等多种疫苗平台。BNT162b2和mRNA-1273是基于mrna的疫苗。疫苗接种似乎对自第一次研究以来出现的SARS-CoV-2菌株有效。它们主要有轻微的副作用,没有重大的安全问题。基于腺病毒的疫苗由基于非复制性腺病毒载体的遗传货物递送,无需佐剂即可增强免疫应答。这就是Ad26.CoV2的情况。S、ChAdOx1 nCoV-19/AZD1222、Gam-COVID-Vac/Sputnik V和基于ad5的COVID-19疫苗。与mRNA疫苗不同,腺病毒疫苗没有已知的过敏发生率。灭活病毒疫苗是一种常见的疫苗形式,已经使用了几十年。目标是使病毒不具有传染性,同时保留高质量抗原的免疫原性,以触发免疫反应。研究的甲醛灭活SARS-CoV2全病毒疫苗(CoronaVac)以及WIV04和HB02都使用了这种疫苗配方。一种名为NVX-CoV2373的重组蛋白纳米颗粒疫苗由三聚体刺突糖蛋白和强效Matrix-M1佐剂组成。针对B.1.1.7 (Alpha)变种,该疫苗似乎非常有效。另一方面,疫苗对B.1.351 (β)菌株的效力较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of the Vaccines, Their Safety, and Immune Responses against SARS-CoV-2 Infections
The search for vaccines has been a high priority since the worldwide COVID-19 pandemic was declared. Currently, mRNA-based vaccines, adenovirus-based vaccines, inactivated virus vaccines, and other vaccine platforms are all employed to combat the SARS-CoV-2 virus. BNT162b2 and mRNA-1273 are mRNA-based vaccines. The vaccination appears to be effective against SARS-CoV-2 strains that have emerged since the first study. They have primarily minor side effects, and there are no major safety concerns. Adenovirus-based vaccines are delivered by genetic cargo that is based on non-replicating adenovirus vectors that can increase immune response without the need of adjuvants. This is the case for Ad26.CoV2.S, ChAdOx1 nCoV-19/AZD1222, Gam-COVID-Vac/Sputnik V andAd5-based COVID-19 vaccine. There have been no known incidences of allergy to adenovirus vaccines, unlike mRNA vaccines. Inactivated virus vaccines are a common form of vaccine that has been used for decades. The goal is to render the virus non-infectious while preserving immunogenicity with high-quality antigens in order to trigger an immune response. The researched formaldehyde-inactivated whole-virus SARS-CoV2 vaccine (CoronaVac), as well as WIV04 and HB02, utilize this sort of vaccine formulation. A recombinant protein nanoparticle vaccine named NVX-CoV2373 is made up of trimeric spike glycoproteins with a potent Matrix-M1 adjuvant. Against the variant B.1.1.7 (Alpha), the vaccine appeared to be very effective. Vaccine efficacy against the B.1.351 (Beta) strain, on the other hand, proved to be lower.
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