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dc.contributor.authorKimutai, Albert
dc.contributor.authorTonui, Willy K
dc.contributor.authorGicheru, Michael M
dc.contributor.authorNgure, Peter Kamau
dc.contributor.authorIngonga, Johnstone
dc.contributor.authorKepha, Stella
dc.contributor.authorNjeru, Laban Ireri
dc.contributor.authorWachira, Dorcas
dc.contributor.authorMuhia, Robert Karanja
dc.contributor.authorMwangi, Milkah
dc.contributor.authorNyamwamu, Lydia B
dc.date.accessioned2015-07-26T08:27:00Z
dc.date.available2015-07-26T08:27:00Z
dc.date.issued2009
dc.identifier.citationJournal of Nanjing Medical University Volume 23, Issue 6, November 2009, Pages 359–372en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S1007437609600848
dc.identifier.urihttp://hdl.handle.net/11295/88829
dc.description.abstractObjective To determine the adjuvant potential of artemisinin with a soluble leishmanial antigen in vaccinating BALB/c mice. Methods Seventy two female BALB/c mice were randomly assigned into six groups. The mice were vaccinated with soluble leishmania antigens (SLA) alone, artemisinin co-administered with SLA, SLA and Bacille Calmette Guérin (BCG) vaccine, and artemisinin and BCG alone. Unvaccinated mice formed the control group. The induction of cell-mediated immunity following vaccination was determined by measuring in vitro lymphocyte proliferation and the production of interleukin (IL)-4, IL-5 and gamma interferon (IFN-γ) determined by flow cytometry. Protection against L. major was determined by quantifying parasite burdens in L. major infected footpads using a limiting dilution assay and by measuring lesion sizes of the infected footpad compared to the contralateral uninfected footpad. Results Mice receiving SLA plus artemisinin produced significantly high levels of IL-4 and IL-5 (P < 0.05) and low levels of IFN-γ, resulting in exacerbated disease. In addition, subcutaneous administration of SLA + artemisinin, artemisinin alone or SLA alone resulted in the development of large footpad swellings and high parasite loads that were comparable to those of the control unvaccinated mice (P > 0.05), resulting in exacerbated disease. Conclusion These data suggest that artemisinin is not a suitable adjuvant for Leishmania vaccines. However, since artemisinin has been shown to be effective against Leishmania parasites in vitro and in vivo, further studies ought to be conducted to determine its immunochemotherapeutic potential when co-administered with Leishmania antigensen_US
dc.language.isoenen_US
dc.subjectArtemisininen_US
dc.subjectLeishmaniaen_US
dc.subjectSoluble Leishmania antigensen_US
dc.subjectCytokineen_US
dc.subjectAdjuvanten_US
dc.subjectInterleukin-4 (IL-4)en_US
dc.subjectIL-5;en_US
dc.subjectIFN-γen_US
dc.subjectBALB/c miceen_US
dc.subjectImmunityen_US
dc.subjectLesion sizeen_US
dc.subjectFootpad lesionen_US
dc.subjectVaccineen_US
dc.subjectParasite burdenen_US
dc.subjectProliferationen_US
dc.subjectStimulation indexen_US
dc.titleEvaluation of the adjuvanticity of artemisinin with soluble Leishmania major antigens in BALB/c miceen_US
dc.typeArticleen_US
dc.type.materialenen_US


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