Immunoprophylaxis of Punta Toro virus ( Phlebovirus , Bunyaviridae ) infection in hamsters with recombinant Eimeria profilin-like antigen
International Immunopharmacology, ISSN: 1567-5769, Vol: 8, Issue: 8, Page: 1089-1094
2008
- 10Citations
- 9Usage
- 13Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations10
- Citation Indexes9
- CrossRef9
- Patent Family Citations1
- 1
- Usage9
- Abstract Views9
- Captures13
- Readers13
- 13
Article Description
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 alone, 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-γ and TNF-α were assessed to evaluate the induction of these inflammatory mediators known to be induced in mice following exposure to rEA. A dose of 100 μg 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-γ 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.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1567576908001100; http://dx.doi.org/10.1016/j.intimp.2008.03.019; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=50949096184&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/18550012; https://linkinghub.elsevier.com/retrieve/pii/S1567576908001100; https://digitalcommons.usu.edu/advs_facpub/659; https://digitalcommons.usu.edu/cgi/viewcontent.cgi?article=1658&context=advs_facpub
Elsevier BV
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