Subunit and Virus-Like Particle Vaccine Approaches for Respiratory Syncytial Virus

被引:16
|
作者
Morrison, Trudy G. [1 ]
Walsh, Edward E. [2 ]
机构
[1] Univ Massachusetts, Dept Microbiol & Physiol Syst, Sch Med, Worcester, MA 01655 USA
[2] Univ Rochester, Sch Med & Dent, Rochester Gen Hosp, Div Infect Dis, Rochester, NY 14621 USA
来源
CHALLENGES AND OPPORTUNITIES FOR RESPIRATORY SYNCYTIAL VIRUS VACCINES | 2013年 / 372卷
关键词
PURIFIED-F-GLYCOPROTEIN; ENHANCED PULMONARY HISTOPATHOLOGY; TOLL-LIKE RECEPTORS; IMMUNE-RESPONSES; FUSION PROTEIN; COTTON RATS; SEROPOSITIVE CHILDREN; ANTIBODY-RESPONSES; INNATE IMMUNITY; RSV CHALLENGE;
D O I
10.1007/978-3-642-38919-1_14
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite its impact on global health, there is no vaccine available for the prevention of respiratory syncytial virus (RSV) infection. Failure to develop a licensed vaccine is not due to lack of effort, as numerous vaccine candidates have been characterized in preclinical and clinical studies spanning five decades. The vaccine candidates thus far explored can be generally divided into four categories: (1) whole inactivated virus, (2) replication competent, attenuated virus including recombinant viruses, (3) gene-based vectors, and (4) subunit and particulate forms of RSV antigens. The first clinically tested RSV vaccine candidate was a formalin-inactivated purified virus preparation administered to infants and children in the late 1960s. Due to the disastrous outcome of these trials and results of animal models investigating the mechanisms involved, there have been no further studies with inactivated RSV vaccines. Rather, efforts have focused on development of other approaches. In this chapter, we review the history and status of purified proteins, peptides, virus-like particles, virosomes, and nanoparticles and discuss their future potential.
引用
收藏
页码:285 / 306
页数:22
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