Experimental cerebral malaria (ECM) is a severe complication of Plasmodium berghei ANKA (PbA) infection in mice, characterized by CD8 T-cell accumulation within the brain. Whilst the dynamics of CD8 T-cell activation and migration during extant primary PbA infection have been extensively researched, the fate of the parasite-specific CD8 T cells upon resolution of ECM is not understood. In this study, we show that memory OT-I cells persist systemically within the spleen, lung and brain following recovery from ECM after primary PbA-OVA infection.
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