Abstract
Background and ObjectiveExtracellular vesicles (EVs) have been described as microparticles produced by different cells in the body with the capacity of mediating cell‐cell communication. A clear mechanism of how various immune cells function during malaria infection is still undergoing investigations. With various states and roles of gamma delta T cells reported, its role in human cerebral malaria has not yet been defined as a study has suggested that it is essential in the development of murine cerebral malaria through its production of interferon gamma and tumor necrosis factor. However, there is currently no report on interactions between EVs derived from Plasmodium falciparum infected red blood cells (iRC‐EVs) and human gamma delta T cells. Our aim therefore, was to investigate the interactions between iRBC‐EVs and gamma delta T cells and the resulting immunological responses that could play a role in the pathogenesis of cerebral malaria.MethodBy using Ultracentrifugation, EVs derived from Plasmodium falciparum infected red blood cell (iRBC‐EVs) culture were isolated and purified. The iRBC‐EVs were characterized by western blot, Fast protein liquid chromatography and electron microscopy. Gamma delta T cells were generated from peripheral blood mononuclear cells(PBMCs) isolated from human blood and stimulated with Plasmodium falciparum culture supernatant and IL‐2 for 14 days. The generated gamma delta T cells were treated with the iRBC‐EVs and monitored for uptake, proliferation and activation using confocal microscopy and flow cytometry.Results and ConclusionWe found out that gamma delta T cells are capable of taking up iRBC‐EVs and were proliferating on co‐incubation with iRBC‐EVs and Plasmodium falciparum culture supernatant. In conclusion, our results show that there is an influence of iRBC‐EVs on gamma delta T cells which would form a basis for further investigations on the immunological responses mediated by these cells towards the development of cerebral malaria.This abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.
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