Nanoparticle vaccines against respiratory syncytial virus

被引:3
|
作者
Stephens, Laura M. [1 ]
Varga, Steven M. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Microbiol & Immunol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
adjuvant; lung; nanoparticle; respiratory syncytial virus; RSV; vaccine; MONOPHOSPHORYL-LIPID-A; T-CELL RESPONSES; IMMUNE-RESPONSE; SILVER NANOPARTICLES; ULTRAFINE PARTICLES; INFLUENZA-VIRUS; DENDRITIC CELLS; FUSION PROTEIN; RISK-FACTORS; BIODEGRADABLE MICROPARTICLES;
D O I
10.2217/fvl-2020-0174
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Respiratory syncytial virus (RSV) is a leading cause of respiratory disease in infants, the elderly and immunocompromised individuals. Despite the global burden, there is no licensed vaccine for RSV. Recent advances in the use of nanoparticle technology have provided new opportunities to address some of the limitations of conventional vaccines. Precise control over particle size and surface properties enhance antigen stability and prolong antigen release. Particle size can also be modified to target specific antigen-presenting cells in order to induce specific types of effector T-cell responses. Numerous nanoparticle-based vaccines are currently being evaluated for RSV including inorganic, polymeric and virus-like particle-based formulations. Here, we review the potential advantages of using different nanoparticle formulations in a vaccine for RSV, and discuss many examples of safe, and effective vaccines currently in both preclinical and clinical stages of testing.
引用
收藏
页码:763 / 778
页数:16
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