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Abstract
Each year over 200 million malaria infections occur with over 400 thousand associated
deaths. Certain vaccines based on attenuated whole parasites can induce protective
memory CD8 T cell responses against liver-stage malaria, however, widespread administration
of such vaccines is logistically challenging. Recent scientific advances are delineating
how protective memory CD8 T cell populations are primed and maintained, and how such
cells mediate immunity to liver-stage malaria. Memory CD8 T cell anatomical localization
and expression of transcription factors, homing receptors, and signaling molecules
appear to play integral roles in protective immunity to liver-stage malaria. Further
investigation of how such factors contribute to optimal protective memory CD8 T cell
generation and maintenance in humans will inform efforts for improved vaccines.