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当前 COVID-19 疫苗平台的成就和差距概述及下一代疫苗的考虑因素。

An Overview of Current Accomplishments and Gaps of COVID-19 Vaccine Platforms and Considerations for Next Generation Vaccines.

机构信息

Vaccine Nanotechnology Laboratory, Center for Drug Delivery and Research, Mercer University, College of Pharmacy, Atlanta, GA, United States.

Innovative Assay Solutions, San Diego, CA, United States.

出版信息

J Pharm Sci. 2023 May;112(5):1345-1350. doi: 10.1016/j.xphs.2023.01.019. Epub 2023 Feb 2.

Abstract

Vaccines against SARS-CoV-2 have transformed the course of the COVID-19 pandemic with more than 30 authorizations. More than 2 billion people have been vaccinated with these vaccines developed on very different manufacturing platforms. We have reviewed the unprecedented work done in various aspects of the authorized vaccines and listed three potential improvements: 1) long-term stability at room-temperature conditions; 2) suitability for diverse populations such as infants, elderly, immune-compromised, and those with pre-existing or ongoing diseases; and 3) ability to act against different strains. In this article, we have discussed the current status of COVID-19 vaccines with respect to 1) diversity (strength and breadth) of initial immune responses and long-term immune memory; 2) prime-boost combinations that induce protection against variants; and 3) breakthrough infections. Further, we have listed host, product (critical quality attributes), and viral pathogenic factors that contribute to safety, efficacy, and effectiveness of vaccines. In addition, we have elaborated on the potential to (develop models and) determine the immune correlates that can predict long-term immune memory. The graphical representation of the abstract is provided as Fig. 1.

摘要

针对 SARS-CoV-2 的疫苗已通过 30 多项授权改变了 COVID-19 大流行的进程。这些疫苗是在完全不同的制造平台上开发的,已有超过 20 亿人接种了这些疫苗。我们回顾了授权疫苗各个方面所做的前所未有的工作,并列出了三个潜在的改进方向:1)在室温条件下的长期稳定性;2)适合不同人群,如婴儿、老年人、免疫功能低下者以及患有现有或正在进行的疾病者;3)能够对抗不同的菌株。在本文中,我们讨论了 COVID-19 疫苗的现状,包括 1)初始免疫反应和长期免疫记忆的多样性(强度和广度);2)诱导对变体保护的加强免疫组合;3)突破性感染。此外,我们还列出了有助于疫苗安全性、有效性和效力的宿主、产品(关键质量属性)和病毒致病因素。此外,我们详细阐述了(开发模型和)确定可预测长期免疫记忆的免疫相关性的潜力。摘要的图形表示如图 1 所示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba99/9891786/775222d23966/gr1_lrg.jpg

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