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Since the demonstration of sterile protection afforded by injection of irradiated sporozoites, CD8+ T cells have been shown to play a significant role in protection from liver-stage malaria. This is, however, dependent on the presence of an extremely high number of circulating effector cells, thought to be necessary to scan, locate and kill infected hepatocytes in the short time that parasites are present in the liver. We utilised an adoptive transfer model to elucidate the kinetics of the effector CD8+ T cell response in the liver following P.berghei sporozoite challenge. Although effector CD8+ T cells require less than 24 hours to find, locate and kill infected hepatocytes, active migration of antigen specific CD8+ T cells into the liver was not observed during the 2-day liver-stage of infection as divided cells were only detected from day 3 post-challenge. However, the percentage of donor cells recruited into division was shown to indicate the level of antigen presentation from infected hepatocytes. By titrating the number of transferred antigen specific effector CD8+ T cells and sporozoites we demonstrate that achieving protection towards liver-stage malaria is reliant on CD8+ T cells being able to locate infected hepatocytes, resulting in a protection threshold dependent on a fine balance between the number of infected hepatocytes and CD8+ T cells present in the liver. With such a fine balance determining protection, achieving high number of CD8+ T cells will be critical to the success of a cell-mediated vaccine against liver-stage malaria.


Journal article


Journal of Immunology


American Association of Immunologists

Publication Date