2016
DOI: 10.1016/j.vaccine.2015.10.027
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Schistosomiasis vaccine candidate Sm14/GLA-SE: Phase 1 safety and immunogenicity clinical trial in healthy, male adults

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Cited by 95 publications
(97 citation statements)
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“…A phase III trial to assess if the combination of rSh28GST and praziquantel would help lower pathologic episodes of S. haematobium infection in infected children was carried out from 2009 to 2012; the findings of which have not yet been published [10]. Similarly, phase I clinical trial data on tolerability and specific immune responses after vaccination of adult, male volunteers in a non-endemic area for schistosomiasis with rSm14/GLA-SE has also shown that the vaccine formulation is safe and immunogenic against schistosomiasis (S. mansoni)[38]. Phase I trial for Sm-TSP-2 (S. mansoni) has been initiated in 2014 and is ongoing [10].…”
Section: Current Status Of Schistosomiasis Vaccinesmentioning
confidence: 99%
“…A phase III trial to assess if the combination of rSh28GST and praziquantel would help lower pathologic episodes of S. haematobium infection in infected children was carried out from 2009 to 2012; the findings of which have not yet been published [10]. Similarly, phase I clinical trial data on tolerability and specific immune responses after vaccination of adult, male volunteers in a non-endemic area for schistosomiasis with rSm14/GLA-SE has also shown that the vaccine formulation is safe and immunogenic against schistosomiasis (S. mansoni)[38]. Phase I trial for Sm-TSP-2 (S. mansoni) has been initiated in 2014 and is ongoing [10].…”
Section: Current Status Of Schistosomiasis Vaccinesmentioning
confidence: 99%
“…7), and for its intended use as a vaccine against schistosomiasis, and potentially bladder cancer, glycosylation can interfere with the antigen's immunogenicity. In addition, all of the immunogenicity and toxicity tests done to date with Sm14 were done using an E. coli-produced antigen, which also lacks glycosylation [33,34]. Therefore, the first step in characterizing the Sm14 produced by P. pastoris was to look for potential glycosylation of the final purified product.…”
Section: Characterization Of Sm14 Expressed By P Pastorismentioning
confidence: 99%
“…Clinical trials have been initiated for the use of this P. pastoris derived Sm14 in both animals and humans [33]. The Pichia produced SM14 antigen immunized with GLA adjuvant induced a broad IgG response with no adverse effects outside of self-limited reactions at the site of injection [34]. The Sm14 antigen in conjunction with the Sm29 antigen has been reported to provide significant protection against S. mansoni in mice [35].…”
Section: Characterization Of Sm14 Expressed By P Pastorismentioning
confidence: 99%
“…Recombinant Sm14, produced in Pichia pastoris , was formulated with glucopyranosyl lipid adjuvant stable emulsion (GLA-SE) and has completed a phase I clinical trial (ClinicalTrials.gov Identifier: NCT01154049), showing that the adjuvanted Sm14 product is well tolerated, safe and highly immunogenic [39]. Vaccination stimulated anti-Sm14-IgG antibodies as well as a strong Th1 biased response as evidenced by γ-interferon production on re-stimulation of cells from individuals in vaccinated subjects [38].…”
Section: Introductionmentioning
confidence: 99%