共 28 条
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.
引用
收藏
页数:7
相关论文