Gold nanorod vaccine for respiratory syncytial virus

被引:53
作者
Stone, Johnw [1 ]
Thornburg, Natalie J. [1 ]
Blum, David L. [1 ]
Kuhn, Sam J. [1 ]
Wright, David W. [2 ]
Crowe, James E., Jr. [1 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Chem, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Sch Med, Vanderbilt Vaccine Ctr, Nashville, TN 37232 USA
关键词
PLACE-EXCHANGE-REACTIONS; F-GLYCOPROTEIN; FUSION PROTEIN; NANOPARTICLES; MORTALITY; INFECTION; DYNAMICS; EPITOPES; METAL;
D O I
10.1088/0957-4484/24/29/295102
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Respiratory syncytial virus (RSV) is a major cause of pneumonia and wheezing in infants and the elderly, but to date there is no licensed vaccine. We developed a gold nanorod construct that displayed the major protective antigen of the virus, the fusion protein (F). Nanorods conjugated to RSV F were formulated as a candidate vaccine preparation by covalent attachment of viral protein using a layer-by-layer approach. In vitro studies using ELISA, electron microscopy and circular dichroism revealed that conformation-dependent epitopes were maintained during conjugation, and transmission electron microscopy studies showed that a dispersed population of particles could be achieved. Human dendritic cells treated with the vaccine induced immune responses in primary human T cells. These results suggest that this vaccine approach may be a potent method for immunizing against viruses such as RSV with surface glycoproteins that are targets for the human immune response.
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页数:7
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