Vaccination of calves using the BRSV nucleocapsid protein in a DNA prime-protein boost strategy stimulates cell-mediated immunity and protects the lungs against BRSV replication and pathology

被引:15
|
作者
Carine, Letellier [1 ]
Mathieu, Boxus [2 ]
Laurent, Rosar [1 ]
Jean-Francois, Toussaint [1 ]
Karl, Walravens [1 ]
Stefan, Roels [1 ]
Gilles, Meyer [3 ]
Jean-Jacques, Letesson [4 ]
Pierre, Kerkhofs [1 ]
机构
[1] Vet & Agrochem Res Ctr, Brussels, Belgium
[2] FUSACx, Gembloux, Belgium
[3] Ecole Natl Vet Toulouse, UMR 1225, INRA, ENVT Interact Hotes Agents Pathogenes, Toulouse, France
[4] Fac Univ Notre Dame Paix, Unite Rech Biol Mol, B-5000 Namur, Belgium
关键词
BRSV; prime-boost; nucleocapsid gene;
D O I
10.1016/j.vaccine.2008.06.100
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Respiratory syncytial virus (RSV) is a major cause of respiratory disease in both cattle and young children. Despite the development of vaccines against bovine (B)RSV, incomplete protection and exacerbation of Subsequent RSV disease have Occurred. In order to circumvent these problems, calves Were vaccinated with the nucleocapsid protein, known to be a major target of CD8(+) T cells in cattle. This was performed according to a DNA prime-protein boost strategy. The results showed that DNA vaccination primed a specific T-cell-mediated response, as indicated by both a lymphoproliferative response and IFN-gamma production. These responses were enhanced after protein boost. After challenge, mock-vaccinated calves displayed gross pneumonic lesions and viral replication in the lungs. In contrast, calves vaccinated by successive administrations of plasmid DNA and protein exhibited protection against the development of pneumonic lesions and the viral replication in the BAL fluids and the lungs. The protection correlated to the cell-mediated immunity and not to the antibody response. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4840 / 4848
页数:9
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