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展望 COVID-19 疫苗 III 期临床试验之外。

Looking beyond COVID-19 vaccine phase 3 trials.

机构信息

International Vaccine Institute, Seoul, Republic of Korea.

Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge School of Clinical Medicine, Cambridge, UK.

出版信息

Nat Med. 2021 Feb;27(2):205-211. doi: 10.1038/s41591-021-01230-y. Epub 2021 Jan 19.

Abstract

After the recent announcement of COVID-19 vaccine efficacy in clinical trials by several manufacturers for protection against severe disease, a comprehensive post-efficacy strategy for the next steps to ensure vaccination of the global population is now required. These considerations should include how to manufacture billions of doses of high-quality vaccines, support for vaccine purchase, coordination of supply, the equitable distribution of vaccines and the logistics of global vaccine delivery, all of which are a prelude to a massive vaccination campaign targeting people of all ages. Furthermore, additional scientific questions about the vaccines remain that should be answered to improve vaccine efficacy, including questions regarding the optimization of vaccination regimens, booster doses, the correlates of protection, vaccine effectiveness, safety and enhanced surveillance. The timely and coordinated execution of these post-efficacy tasks will bring the pandemic to an effective, and efficient, close.

摘要

在几家制造商公布了 COVID-19 疫苗在临床试验中的功效,可有效预防重症疾病后,现在需要制定一个全面的后续功效策略,以确保全球人口接种疫苗。这些考虑因素应包括如何生产数十亿剂高质量疫苗,为疫苗采购提供支持,协调供应,公平分配疫苗以及进行全球疫苗输送的后勤工作,所有这些都是针对所有年龄段人群开展大规模疫苗接种运动的前奏。此外,关于疫苗仍存在一些需要解答的科学问题,以提高疫苗的功效,包括有关优化疫苗接种方案、加强针、保护相关因素、疫苗有效性、安全性和加强监测的问题。及时协调地执行这些后续功效任务,将有效地、高效地结束疫情。

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