Search

Circulating memory CD8 T cell trafficking and protective capacity during liver-stage malaria infection remains undefined. We find that effector memory CD8 T cells (Tem) infiltrate the liver within 6 hours after malarial or bacterial infections and mediate pathogen clearance. Tem recruitment coincides with rapid transcriptional upregulation of inflammatory genes in Plasmodium-infected livers. Recruitment requires CD8 T cell-intrinsic LFA-1 expression and the presence of liver phagocytes. Rapid Tem liver infiltration is distinct from recruitment to other non-lymphoid tissues in that it occurs both in the absence of liver tissue resident memory "sensing-and-alarm" function and ∼42 hours earlier than in lung infection by influenza virus. These data demonstrate relevance for Tem in protection against malaria and provide generalizable mechanistic insights germane to control of liver infections., Competing Interests: Declarations of interests The authors declare no competing interests., (Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.)

Lung-resident primary memory CD8 + T cell populations (T rm ) induced by a single influenza infection decline within months, rendering the host susceptible to new heterosubtypic influenza infections. Here, we demonstrate that, relative to single virus exposure, repeated antigen exposure dramatically alters the dynamics of influenza-specific lung T rm populations. Lung T rm derived from repeatedly stimulated circulating memory CD8 + T cells exhibit extended durability and protective heterosubtypic immunity relative to primary lung T rm . Parabiosis studies reveal that the enhanced durability of lung T rm after multiple antigen encounters resulted from the generation of long-lasting circulating effector memory (T em ) populations, which maintained the ability to be recruited to the lung parenchyma and converted to T rm , in combination with enhanced survival of these cells in the lung. Thus, generating a long-lasting T rm precursor pool through repeated intranasal immunizations might be a promising strategy to establish long-lasting lung T rm -mediated heterosubtypic immunity against influenza., (Copyright © 2018 The Author(s). Published by Elsevier Inc. All rights reserved.)