COVID-19 vaccine: recent advancements and future prospects

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2024-07-05 DOI:10.1002/mco2.646
Li Xu, Min Li, Wu He
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引用次数: 0

Abstract

Nowadays, although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) epidemic has been handled with long-term management globally, the virus strains keep continuous evolution in an uncertain direction. The newly emerged JN.1 dominated the globally circulating variants in a short time and resulted in increasing hospitalizations. Up to 2024, variant vaccines with the composition of XBB sub-lineage were available due to the coordinated efforts of developers and regulatory agencies. The development of updated vaccines is still needed and the regular availability of coronavirus disease 2019 (COVID-19) vaccines should be timely guaranteed. The current landscape of COVID-19 vaccines and the strategies for accelerating vaccine development and approval are reviewed. Proposals to enhance variants monitoring and the establishment of the strain recommendation mechanism are made. This review provides suggestions about platform technology designation and application, real-world data leveraging and modification to regulatory pathways both for the post-pandemic era of SARS-CoV-2 and for the future unknown pathogen pandemic.

COVID-19 疫苗:最新进展与未来展望
目前,虽然全球对严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)疫情进行了长期管理,但病毒株仍在朝着不确定的方向不断演变。新出现的 JN.1 在短时间内占据了全球流行变异株的主导地位,导致住院人数不断增加。在研发人员和监管机构的共同努力下,截至 2024 年,XBB 亚系变异疫苗已经问世。目前仍需开发更新疫苗,并应及时保证冠状病毒病 2019(COVID-19)疫苗的正常供应。本文回顾了 COVID-19 疫苗的现状以及加快疫苗研发和审批的策略。提出了加强变异株监测和建立毒株推荐机制的建议。本综述就 SARS-CoV-2 后大流行时代和未来未知病原体大流行的平台技术指定和应用、真实世界数据利用和监管途径修改提出了建议。
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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来源期刊
CiteScore
6.70
自引率
0.00%
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0
审稿时长
10 weeks
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