| Literature DB >> 24397898 |
Souvik Karmakar1, Weidong Zhang1, Gul Ahmad2, Workineh Torben3, Mayeen U Alam1, Loc Le1, Raymond T Damian4, Roman F Wolf5, Gary L White5, David W Carey5, Darrick Carter6, Steven G Reed7, Afzal A Siddiqui8.
Abstract
The ability of the Schistosoma mansoni antigen, Sm-p80, to provide cross-species protection against Schistosoma haematobium challenge was evaluated in hamster and baboon models. Pronounced reduction in worm burden (48%) and in tissue egg load (64%) was observed in hamsters vaccinated with recombinant Sm-p80 admixed with glucopyranosyl lipid adjuvant-stable emulsion (GLA-SE). Similarly, in baboons, the Sm-p80/GLA-SE vaccine produced a 25% reduction in S. haematobium adult worms and decreased the egg load in the urinary bladder by 64%. A 40% and 53% reduction in fecal and urine egg output, respectively, was observed in vaccinated baboons. A balanced pro-inflammatory (Th17 and Th1) and Th2 type of response was generated after vaccination and appears indicative of augmented prophylactic efficacy. These data on cross-species protection coupled with the prophylactic, therapeutic and antifecundity efficacy against the homologous parasite, S. mansoni, reinforces Sm-p80 as a promising vaccine candidate. It is currently being prepared for GMP-compliant manufacture and for further pre-clinical development leading to human clinical trials. These results solidify the expectation that the Sm-p80 vaccine will provide relief for both the intestinal and the urinary schistosomiasis and thus will be greatly beneficial in reducing the overall burden of schistosomiasis.Entities:
Keywords: Baboons; Calpain; Intestinal schistosomiasis; Nonhuman primate; Schistosoma haematobium; Schistosoma mansoni; Schistosome vaccine; Sm-p80; Urinary schistosomiasis
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Year: 2014 PMID: 24397898 PMCID: PMC3934627 DOI: 10.1016/j.vaccine.2013.12.057
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641