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Open Forum Infect Dis. 2022 Apr 18;9(6):ofac138. doi: 10.1093/ofid/ofac138. eCollection 2022 Jun.
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Plant-Based Vaccines in Combat against Coronavirus Diseases.对抗冠状病毒疾病的植物源疫苗
Vaccines (Basel). 2022 Jan 18;10(2):138. doi: 10.3390/vaccines10020138.
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SARS-CoV-2 DNA Vaccine INO-4800 Induces Durable Immune Responses Capable of Being Boosted in a Phase 1 Open-Label Trial.SARS-CoV-2 DNA 疫苗 INO-4800 可诱导持久的免疫应答,并在 1 期开放标签试验中进行了加强。
J Infect Dis. 2022 Jun 1;225(11):1923-1932. doi: 10.1093/infdis/jiac016.
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J Virol. 2022 Mar 9;96(5):e0167521. doi: 10.1128/JVI.01675-21. Epub 2022 Jan 5.
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Advances in the design and development of SARS-CoV-2 vaccines.SARS-CoV-2 疫苗的设计和开发进展。
Mil Med Res. 2021 Dec 16;8(1):67. doi: 10.1186/s40779-021-00360-1.
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Safety and immunogenicity of ChAdOx1 MERS vaccine candidate in healthy Middle Eastern adults (MERS002): an open-label, non-randomised, dose-escalation, phase 1b trial.ChAdOx1 MERS 候选疫苗在健康中东成年人中的安全性和免疫原性(MERS002):一项开放标签、非随机、剂量递增、1b 期临床试验。
Lancet Microbe. 2022 Jan;3(1):e11-e20. doi: 10.1016/S2666-5247(21)00193-2. Epub 2021 Nov 3.
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Neutralizing Antibodies against SARS-CoV-2, Anti-Ad5 Antibodies, and Reactogenicity in Response to Ad5-nCoV (CanSino Biologics) Vaccine in Individuals with and without Prior SARS-CoV-2.有或无SARS-CoV-2既往感染史个体中针对SARS-CoV-2的中和抗体、抗Ad5抗体以及对Ad5-nCoV(康希诺生物)疫苗的反应原性
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COVID-19 vaccines.新型冠状病毒疫苗。
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Safety, tolerability, and immunogenicity of an aerosolised adenovirus type-5 vector-based COVID-19 vaccine (Ad5-nCoV) in adults: preliminary report of an open-label and randomised phase 1 clinical trial.一种雾化型腺病毒 5 型载体新冠疫苗(Ad5-nCoV)在成年人中的安全性、耐受性和免疫原性:一项开放标签、随机 1 期临床试验的初步报告。
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The CEPI centralised laboratory network: supporting COVID-19 vaccine development.流行病防范创新联盟(CEPI)集中实验室网络:支持新冠疫苗研发
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全球调查 COVID-19 可能的疫苗接种策略的发展情况。

A global survey in the developmental landscape of possible vaccination strategies for COVID-19.

机构信息

Société Francophone de Nutrithérapie et de Nutrigénétique Appliquée, Villeurbanne, France.

Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.

出版信息

Clin Immunol. 2022 Apr;237:108958. doi: 10.1016/j.clim.2022.108958. Epub 2022 Feb 24.

DOI:10.1016/j.clim.2022.108958
PMID:35218966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8865932/
Abstract

The development of COVID-19 vaccines was promptly regulated to ensure the best possible approach. By January 2022, 75 candidates reached preclinical evaluation in various animal models, 114 vaccines were in clinical trials on humans, and 48 were in the final testing stages. Vaccine platforms range from whole virus vaccines to nucleic acid vaccines, which are the most promising in prompt availability and safety. The USA and Europe have approved vaccines developed by Pfizer-BioNTech (BNT162b2) and Moderna (mRNa1273). So far, Pfizer-BioNTech, Moderna, Johnson & Johnson, AstraZeneca-University of Oxford, Sinopharm, Sinovac Biotech Gamaleya, Bharat Biotech, and Novavax have documented effective vaccines. Even with technological advances and a fast-paced development approach, many limitations and problems need to be overcome before a large-scale production of new vaccines can start. The Key is to ensure equal and fair distribution globally through regulatory measures. Recent studies link Bacillus Calmette-Guérin (BCG) vaccination programs and lower disease severity.

摘要

COVID-19 疫苗的研发得到了迅速规范,以确保采用最佳方法。截至 2022 年 1 月,75 种候选疫苗在各种动物模型中完成了临床前评估,114 种疫苗已在人体临床试验中,48 种处于最终测试阶段。疫苗平台涵盖从全病毒疫苗到核酸疫苗,核酸疫苗在即时可用性和安全性方面最具前景。美国和欧洲已批准辉瑞-生物科技(BNT162b2)和莫德纳(mRNA1273)研发的疫苗。到目前为止,辉瑞-生物科技、莫德纳、强生、阿斯利康-牛津大学、国药集团、科兴中维 Gamaleya 研究所、巴拉特生物技术公司和诺瓦瓦克斯已证明有效疫苗。即使有技术进步和快速发展方法,在大规模生产新疫苗之前,仍需要克服许多限制和问题。关键是通过监管措施确保全球平等和公平分配。最近的研究表明,卡介苗(BCG)接种计划与降低疾病严重程度有关。