Safety and Mechanism of Action of Licensed Vaccine Adjuvants

D. S. Rambe, G. Giudice, S. Rossi, Melvin Sanicas
{"title":"Safety and Mechanism of Action of Licensed Vaccine Adjuvants","authors":"D. S. Rambe, G. Giudice, S. Rossi, Melvin Sanicas","doi":"10.3329/ICPJ.V4I8.24024","DOIUrl":null,"url":null,"abstract":"Vaccines are some of the most effective tools for the prevention of infectious diseases. Adjuvants are included in vaccines for a variety of reasons: to increase the breadth of response, to lower antigen dose, to overcome limited immune response in some populations, or to enable complex combination vaccines. This study aims to review the safety of licensed vaccine adjuvants and describe their mechanism of action. Potential publications for inclusion were identified through a direct search of PubMed/Medline database. Results of online literature searches were supplemented by relevant papers cited in published studies along with the authors' knowledge of published studies. To date, there are 5 licensed vaccine adjuvants in US and Europe: Aluminum salts (EU, US), MF59 (EU), AS03 (EU), AS04 (EU, US), and virosomes (EU). AS03 is not available as an adjuvant in other vaccines but included within the US government's National Stockpile. All vaccines that contain these adjuvants have been proven safe in clinical trials and post-marketing studies, with the exception of the AS03, for which the rare events of narcolepsy have been reported in some countries. Every adjuvant has a complex and often multifactorial immunological mechanism, usually poorly understood in vivo. The safety profile of an adjuvant, including the actual and hypothetical risks, is a critical component that can speed up or impede adjuvant development. The increasing understanding in adjuvant sciences is fundamental to the further development of new adjuvants.","PeriodicalId":13811,"journal":{"name":"International Current Pharmaceutical Journal","volume":"102 1","pages":"420-431"},"PeriodicalIF":0.0000,"publicationDate":"2015-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"22","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Current Pharmaceutical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/ICPJ.V4I8.24024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 22

Abstract

Vaccines are some of the most effective tools for the prevention of infectious diseases. Adjuvants are included in vaccines for a variety of reasons: to increase the breadth of response, to lower antigen dose, to overcome limited immune response in some populations, or to enable complex combination vaccines. This study aims to review the safety of licensed vaccine adjuvants and describe their mechanism of action. Potential publications for inclusion were identified through a direct search of PubMed/Medline database. Results of online literature searches were supplemented by relevant papers cited in published studies along with the authors' knowledge of published studies. To date, there are 5 licensed vaccine adjuvants in US and Europe: Aluminum salts (EU, US), MF59 (EU), AS03 (EU), AS04 (EU, US), and virosomes (EU). AS03 is not available as an adjuvant in other vaccines but included within the US government's National Stockpile. All vaccines that contain these adjuvants have been proven safe in clinical trials and post-marketing studies, with the exception of the AS03, for which the rare events of narcolepsy have been reported in some countries. Every adjuvant has a complex and often multifactorial immunological mechanism, usually poorly understood in vivo. The safety profile of an adjuvant, including the actual and hypothetical risks, is a critical component that can speed up or impede adjuvant development. The increasing understanding in adjuvant sciences is fundamental to the further development of new adjuvants.
许可疫苗佐剂的安全性和作用机制
疫苗是预防传染病最有效的工具之一。在疫苗中加入佐剂有多种原因:增加反应的广度,降低抗原剂量,克服某些人群中有限的免疫反应,或使复杂的联合疫苗成为可能。本研究旨在回顾已批准的疫苗佐剂的安全性,并描述其作用机制。通过直接检索PubMed/Medline数据库确定可能纳入的出版物。网络文献检索的结果由已发表研究中引用的相关论文以及作者对已发表研究的了解来补充。迄今为止,在美国和欧洲有5种获得许可的疫苗佐剂:铝盐(EU, US)、MF59 (EU)、AS03 (EU)、AS04 (EU, US)和病毒体(EU)。AS03不能作为其他疫苗的佐剂,但被列入美国政府的国家储备。所有含有这些佐剂的疫苗都已在临床试验和上市后研究中被证明是安全的,但AS03疫苗除外,在一些国家报告了罕见的发作性睡病事件。每一种佐剂都有一个复杂的、往往是多因素的免疫机制,通常在体内知之甚少。佐剂的安全性,包括实际和假设的风险,是加速或阻碍佐剂发展的关键因素。对佐剂科学的日益了解是新佐剂进一步开发的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信