Nature Communications (Feb 2024)

A hepatic network of dendritic cells mediates CD4 T cell help outside lymphoid organs

  • Kieran English,
  • Rain Kwan,
  • Lauren E. Holz,
  • Claire McGuffog,
  • Jelte M. M. Krol,
  • Daryan Kempe,
  • Tsuneyasu Kaisho,
  • William R. Heath,
  • Leszek Lisowski,
  • Maté Biro,
  • Geoffrey W. McCaughan,
  • David G. Bowen,
  • Patrick Bertolino

DOI
https://doi.org/10.1038/s41467-024-45612-5
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 17

Abstract

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Abstract While CD4+ T cells are a prerequisite for CD8+ T cell-mediated protection against intracellular hepatotropic pathogens, the mechanisms facilitating the transfer of CD4-help to intrahepatic CD8+ T cells are unknown. Here, we developed an experimental system to investigate cognate CD4+ and CD8+ T cell responses to a model-antigen expressed de novo in hepatocytes and reveal that after initial priming, effector CD4+ and CD8+ T cells migrate into portal tracts and peri-central vein regions of the liver where they cluster with type-1 conventional dendritic cells. These dendritic cells are locally licensed by CD4+ T cells and expand the number of CD8+ T cells in situ, resulting in larger effector and memory CD8+ T cell pools. These findings reveal that CD4+ T cells promote intrahepatic immunity by amplifying the CD8+ T cell response via peripheral licensing of hepatic type-1 conventional dendritic cells and identify intrahepatic perivascular compartments specialized in facilitating effector T cell-dendritic cell interactions.