Strategic evaluation of vaccine candidate antigens for the prevention of Visceral Leishmaniasis. Issue 25 (27th May 2016)

• Record Type: Journal Article
• Authors: Duthie, Malcolm S.; Favila, Michelle; Hofmeyer, Kimberley A.; Tutterrow, Yeung L.; Reed, Steven J.; Laurance, John D.; Picone, Alessandro; Guderian, Jeffrey; Bailor, H. Remy; Vallur, Aarthy C.; Liang, Hong; Mohamath, Raodoh; Vergara, Julie; Howard, Randall F.; Coler, Rhea N.; Reed, Steven G.
• Is Part Of: Vaccine. Volume 34:Issue 25(2016)
• Page Start: 2779
• Page End: 2786
• Publication Date: 2016-05-27
• Subjects: Leishmania -- T cell -- Protein -- Protozoa -- Vaccine; CL cutaneous leishmaniasis -- GLA-SE glucopyranosyl lipid adjuvant in stable emulsion -- H2B histone H2B -- MDH malate dehydrogenase -- SDS-PAGE sodium dodecyl sulfate-polyacrylamide gel electrophoresis -- SMT sterol methyltransferase -- TLR Toll-like receptor -- VL visceral leishmaniasis; Vaccines -- Periodicals; 615.372
• DOI: 10.1016/j.vaccine.2016.04.067
• Languages: English
• ISSNs: 0264-410X

Abstract

Abstract: Infection with Leishmania parasites results in a range of clinical manifestations and outcomes, the most severe of which is visceral leishmaniasis (VL). Vaccination will likely provide the most effective long-term control strategy, as the large number of vectors and potential infectious reservoirs renders sustained interruption of Leishmania parasite transmission extremely difficult. Selection of the best vaccine is complicated because, although several vaccine antigen candidates have been proposed, they have emerged following production in different platforms. To consolidate the information that has been generated into a single vaccine platform, we expressed seven candidates as recombinant proteins in E. coli . After verifying that each recombinant protein could be recognized by VL patients, we evaluated their protective efficacy against experimental L. donovani infection of mice. Administration in formulation with the Th1-potentiating adjuvant GLA-SE indicated that each antigen could elicit antigen-specific Th1 responses that were protective. Considering the ability to reduce parasite burden along with additional factors such as sequence identity across Leishmania species, we then generated a chimeric fusion protein comprising a combination of the 8E, p21 and SMT proteins. This E. coli –expressed fusion protein was also demonstrated to protect against L. donovani infection. These data indicate a novel recombinant vaccine antigen with the potential for use in VL control programs.