布莱顿合作标准化模板,其中包含对基于非复制改良疫苗病毒安卡拉病毒载体的病毒载体疫苗进行效益/风险评估的主要考虑因素

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Ellen K. Link , Alina Tscherne , Gerd Sutter , Emily R. Smith , Marc Gurwith , Robert T. Chen , Asisa Volz , For the Benefit-Risk Assessment of VAccines by TechnolOgy Working Group (BRAVATO; ex-V3SWG)
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引用次数: 0

摘要

布莱顿技术疫苗效益-风险评估合作组织 (BRAVATO) 成立的目的是评估新平台技术疫苗的安全性和其他关键特征。本手稿概述了安卡拉改良型疫苗(MVA),并回顾了该平台的分子和生物学关键特征。该疫苗已在不同的临床前动物模型中进行了成功评估,并接受了临床测试,包括一项有 170 多人参与的 Ib 期研究。在这种情况下,新出现的人畜共患传染病对公共卫生系统构成了特别的挑战。在过去二十年中,出现了三种不同的呼吸道冠状病毒,包括中东呼吸综合征冠状病毒(MERS-CoV)。多年来,安全有效的疫苗一直是抗击传染病的主要工具。在此,我们报告了一种基于 MVA 的抗 MERS-CoV 候选疫苗(MVA-MERS-S)。应用后,MVA-MERS-S 具有良好的耐受性和免疫原性,可在不同的动物模型和人体中诱导细胞和体液免疫反应。我们以 MVA-MERS-S 为例证明,MVA 载体平台是生产安全、免疫原性和高效的新发传染病疫苗的可行而有效的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Brighton collaboration standardized template with key considerations for a benefit/risk assessment for a viral vector vaccine based on a non-replicating modified vaccinia virus Ankara viral vector
The Brighton Collaboration Benefit-Risk Assessment of VAccines by TechnolOgy (BRAVATO) was formed to evaluate the safety and other key features of new platform technology vaccines. This manuscript provides an overview of Modified Vaccinia virus Ankara (MVA)-vectored vaccines and reviews molecular and biological key features of this platform. In particular, this review aims to provide fundamental information about the promising candidate vaccine MVA-MERS-S which has been evaluated successfully in different preclinical animal models and has undergone clinical testing including a phase Ib study involving more than 170 participants.
Infectious diseases continue to be a major cause of human death worldwide. In this context, emerging zoonotic infectious diseases pose a particular challenge for public health systems. In the last two decades, three different respiratory coronaviruses, including the Middle East respiratory syndrome Coronavirus (MERS-CoV) have emerged. For many years, safe and efficacious vaccines have been a major tool to combat infectious diseases.
Here, we report on a promising candidate vaccine (MVA-MERS-S) against MERS-CoV based on MVA. Upon application, MVA-MERS-S has been well tolerated and immunogenic, inducing both, cellular and humoral immune responses in different animal models and humans. We demonstrate that the MVA vector platform, with the example of MVA-MERS-S, is a viable and effective tool for producing safe, immunogenic, and efficient vaccines against emerging infectious diseases.
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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