Immunoprophylaxis of Punta Toro virus (Phlebovirus, Bunyaviridae) infection in hamsters with recombinant Eimeria profilin-like antigen

被引:9
作者
Gowen, Brian B. [1 ,2 ]
Judge, John W. [3 ]
Wong, Min-Hui [1 ,2 ]
Jung, Kie-Hoon [1 ,2 ]
Aylsworth, Charles F. [3 ,4 ]
Melby, Peter C. [5 ,6 ]
Rosenberg, Barnett
Morrey, John D. [1 ,2 ]
机构
[1] Utah State Univ, Inst Antiviral Res, Logan, UT 84322 USA
[2] Utah State Univ, Dept Anim Dairy & Vet Sci, Logan, UT 84322 USA
[3] Barros Res Inst, Holt, MI USA
[4] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[5] Univ Texas Hlth Sci Ctr San Antonio, Res Serv, S Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA
[6] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA
关键词
Punta Toro virus; Phlebovirus; antiviral; immune modulator; profilin;
D O I
10.1016/j.intimp.2008.03.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recombinant Eimeria antigen (rEA) has been shown to have potent anticancer and antiviral activity in respective mouse disease models, presumably through robust immune stimulation that occurs via TLR11, a pattern recognition receptor that recognizes profilin-like proteins expressed on apicomplexan protozoans. Comparable immunostimulatory activity in other species has yet to be demonstrated. Since rEA is known to be highly effective in treating Punta Toro virus (PTV) infection in mice, its ability to elicit protective immunity in the hamster PTV infection model was investigated. rEA was given atone, or in combination with IL-18 or IL-2, and virally challenged hamsters were observed for mortality. Cytokine transcript profiles for IL-12p40, IL-21, IFN-gamma and TNF-alpha were assessed to evaluate the induction of these inflammatory mediators known to be induced in mice following exposure to rEA. A dose of 100 mu g of rEA, given once 4 h prior to viral challenge, and a second time on day 3 of the infection, was found to be the most effective prophylactic therapy protecting 60% of treated hamsters from mortality, compared to only 5-10% observed in animals receiving placebo. Increased expression of IFN-gamma and IL-12p40 was evident following treatment with rEA. The data suggest that rEA does induce host antiviral responses in hamsters that result in significant protection from death, although determining the most appropriate dose for intervention in other species, including humans, will likely be challenging. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1089 / 1094
页数:6
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