Is a universal influenza vaccine feasible?

Q2 Medicine
Therapeutic Advances in Vaccines and Immunotherapy Pub Date : 2019-11-07 eCollection Date: 2019-01-01 DOI:10.1177/2515135519885547
Joshua E Phillipson, Ron Babecoff, Tamar Ben-Yedidia
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引用次数: 3

Abstract

The influenza virus causes significant human morbidity and mortality annually and poses a pandemic threat. In addition, the virus frequently mutates, contributing to thousands of identified strains. Current influenza vaccine solutions are strain specific, target existing strains, and achieve only approximately 40% vaccine effectiveness (VE). The need for broadly protective Universal Influenza Vaccines (UIVs) is clear. UIV research and development efforts focus on widely conserved (i.e. not strain specific) influenza epitopes. The most clinically advanced UIV candidate, the Multimeric-001 (M-001), is currently undergoing a pivotal, clinical efficacy, phase III trial. Completed clinical trials indicate M-001 is safe, well tolerated, and immunogenic to a broad range of influenza strains. Additional candidates are also under development, supported by public and private funding. Research results suggest that it is only a matter of time until a broadly protective influenza vaccine is approved for licensure.

Abstract Image

通用流感疫苗是否可行?
流感病毒每年造成大量人类发病率和死亡率,并构成大流行威胁。此外,该病毒经常变异,导致数千种已确定的毒株。目前的流感疫苗解决方案是针对毒株的,针对现有的毒株,仅能达到约40%的疫苗有效性(VE)。对具有广泛保护性的通用流感疫苗(UIVs)的需求是明确的。艾滋病毒研究和开发工作的重点是广泛保守的(即不是菌株特异性的)流感表位。临床最先进的UIV候选药物是Multimeric-001 (M-001),目前正在进行一项关键的临床疗效III期试验。已完成的临床试验表明,M-001是安全的,耐受性良好,对多种流感毒株具有免疫原性。在公共和私人资金的支持下,其他候选项目也正在开发中。研究结果表明,一种具有广泛保护作用的流感疫苗获得许可只是时间问题。
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
Therapeutic Advances in Vaccines and Immunotherapy
Therapeutic Advances in Vaccines and Immunotherapy Medicine-Pharmacology (medical)
CiteScore
5.10
自引率
0.00%
发文量
15
审稿时长
8 weeks
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