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dc.contributor.authorMuindi, Amy Mwende
dc.date.accessioned2014-07-04T08:47:23Z
dc.date.available2014-07-04T08:47:23Z
dc.date.issued1998
dc.identifier.citationBachelor of Science Zoologyen_US
dc.identifier.urihttp://hdl.handle.net/11295/71801
dc.description.abstractPeople living in schistosomiasis endemic areas, constantly get re-infected with the disease after treatment and it is unknown what the effects of treatment are on the development of immune responses in such situations of parasite exposure and re-exposure. Also, the immunodulatory cytokine, Interleukin-12 (IL-12), derived from natural killer cells and B cells has been reported in mouse studies to influence the outcome of schistosomiasis in animals primed with it prior to infection. It exerts it's role by modifying the balance of T cell sub-populations so that Th-I cells predominate as determined by the presence of cytokines such as interferon gamma (INF-y), interleukin-4 (IL-4) and interleukin-5 (IL-S). This study was divided into two parts. The first part, experiment 1, was designed to examine the effects of treatment and re-infection on antibody responses while the second part, experiment 2, was carried out to examine the influence of the immunodulatory molecule, IL-12 on cytokine (IL-4 and IL-S) production in baboon schistosomiasis. For the first experiment, baboons were given a primary infection of Schistosoma mansoni cercariae (either single -SI or multiple -MI), treated with praziquantel and then given a single or multiple secondary infection. That is, SVSI, SVMI, MIIMI and MIlS!. For the second experiment, baboons were primed with ova alone, IL-12 + ova, IL-12 alone or with saline (control) and later infected with S. mansoni cercariae. The serum samples obtained at various time points during the course of the study were exposed to Enzyme Linked Immunosorbent Assays (ELISAs) and the absorbance readings (40Snm) taken. Results showed that single primary exposure to S. mansoni parasites in baboons, causes severe pathology than multiple primary exposure, while antibody levels after re-infection following treatment, show a modulation of the disease with relatively mild pathology irrespective of single or multiple re-infection doses. It was also observed that, there is no clear-cut difference between the role of IL-4 and IL- S from that of IL-12 in baboon S. mansoni infections because they all play a role of healing, by modulating the pathology due to the disease.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.titleSchistosoma Mansoni Humoral Responses Associated With Re-infection After Treatment And After Priming With Interleukin-12 In Baboonsen_US
dc.typeThesisen_US
dc.type.materialenen_US


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