Canine adenoviruses elicit both humoral and cell-mediated immune responses against rabies following immunisation of sheep

被引:19
|
作者
Bouet-Cararo, Coraline [1 ]
Contreras, Vanessa [2 ]
Fournier, Annie [1 ]
Jallet, Corinne [3 ]
Guibert, Jean Michel [4 ]
Dubois, Eric [4 ]
Thiery, Richard [4 ]
Breard, Emmanuel [1 ]
Tordo, Noel [3 ]
Richardson, Jennifer [1 ]
Schwartz-Cornil, Isabelle [2 ]
Zientara, Stephan [1 ]
Klonjkowski, Bernard [1 ]
机构
[1] ANSES INRA ENVA, UMR Virol 1161, Maisons Alfort, France
[2] INRA, UR 892, Jouy En Josas, France
[3] Inst Pasteur, Dept Virol, Unite Strategies Antivirales, URA 3015, F-75015 Paris, France
[4] ANSES, Unite Pathol Petits Ruminants, Sophia Antipolis, France
关键词
Canine adenovirus; Vaccine; Ovine; VACCINIA VIRUS RECOMBINANT; ORAL VACCINATION; UNITED-STATES; GLYCOPROTEIN; INFECTION; VECTORS; DOGS; FOX; EPIDEMIOLOGY; PROTECTION;
D O I
10.1016/j.vaccine.2010.11.068
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Safe and efficient vaccination is important for rabies prevention in domestic animals. Replicative vectors expressing the rabies virus glycoprotein, derived from canine adenovirus have been reported to be promising vaccines in various animal models. In this paper we compare the potential of a replicative and a non-replicative vector, both based on canine adenovirus type 2 and expressing the rabies glycoprotein. Upon inoculation in sheep, immune responses against the rabies virus protein elicited by recombinant vectors were monitored. All immunised sheep produced a rapid and potent neutralizing antibody response against rabies virus after a single inoculation of either replicative or non-replicative recombinant canine adenovirus type 2. In addition, the non-replicative vector expressing the rabies glycoprotein stimulated antigen-specific CD4(+) and CD8(+) lymphocyte proliferation as well as IFN-gamma production. These results suggest that vectors derived from canine adenovirus 2 could be considered for the development of promising vaccines in the ruminant species. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1304 / 1310
页数:7
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