Abstract
Prophylactic efficacy of Sm-p80 was tested in the mouse model using DNA priming and boosting with protein approach. However, the novelty of the approach utilized in this study is that both the DNA priming and protein boosting was performed on a single day and no further vaccine inoculations were given to mice; the animals were challenged 1 month after the initial vaccine administration. Using this approach, significant reduction in worm burden (33 to 57 %) and marked decrease in egg retention in tissues (34 to 66 %) was observed. Robust antibody titers and upregulation of cytokines (IL-1α/β, IL-12α, and IFN-γ) appears to correlate with the protection. This approach of administering vaccine on a single day could be greatly helpful in the field setting because it will eliminate the compliance issues that may arise with multiple boosters that may be required for optimal efficacy for some vaccines.
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Acknowledgments
This work was supported in part by a grant from National Institute of Allergy and Infectious Diseases (R01A171223) to Afzal A. Siddiqui. The snails were supplied through a NIH-NIAID contract (HHSN2722010000051) to Biomedical Research Institute.
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Loc Le and Weidong Zhang have contributed equally to the study and should be considered as first authors.
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Le, L., Zhang, W., Karmakar, S. et al. Simultaneous priming with DNA encoding Sm-p80 and boosting with Sm-p80 protein confers protection against challenge infection with Schistosoma mansoni in mice. Parasitol Res 113, 1195–1200 (2014). https://doi.org/10.1007/s00436-014-3757-4
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DOI: https://doi.org/10.1007/s00436-014-3757-4