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

Author

Listed:
  • Kieran English

    (Royal Prince Alfred Hospital
    VIB-UGent Center for Inflammation Research)

  • Rain Kwan

    (Royal Prince Alfred Hospital)

  • Lauren E. Holz

    (University of Melbourne)

  • Claire McGuffog

    (Royal Prince Alfred Hospital)

  • Jelte M. M. Krol

    (Royal Prince Alfred Hospital
    Leiden University Medical Centre)

  • Daryan Kempe

    (University of New South Wales)

  • Tsuneyasu Kaisho

    (Wakayama Medical University)

  • William R. Heath

    (University of Melbourne)

  • Leszek Lisowski

    (The University of Sydney
    Military Institute of Medicine)

  • Maté Biro

    (University of New South Wales)

  • Geoffrey W. McCaughan

    (Royal Prince Alfred Hospital)

  • David G. Bowen

    (Royal Prince Alfred Hospital)

  • Patrick Bertolino

    (Royal Prince Alfred Hospital)

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.

Suggested Citation

  • 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. B, 2024. "A hepatic network of dendritic cells mediates CD4 T cell help outside lymphoid organs," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-45612-5
    DOI: 10.1038/s41467-024-45612-5
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    1. Stephen T. Ferris & Vivek Durai & Renee Wu & Derek J. Theisen & Jeffrey P. Ward & Michael D. Bern & Jesse T. Davidson & Prachi Bagadia & Tiantian Liu & Carlos G. Briseño & Lijin Li & William E. Gillan, 2020. "cDC1 prime and are licensed by CD4+ T cells to induce anti-tumour immunity," Nature, Nature, vol. 584(7822), pages 624-629, August.
    2. Alexandre P. Bénéchet & Giorgia Simone & Pietro Lucia & Francesco Cilenti & Giulia Barbiera & Nina Bert & Valeria Fumagalli & Eleonora Lusito & Federica Moalli & Valentina Bianchessi & Francesco Andre, 2019. "Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming," Nature, Nature, vol. 574(7777), pages 200-205, October.
    3. John Paul Ridge & Francesca Di Rosa & Polly Matzinger, 1998. "A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell," Nature, Nature, vol. 393(6684), pages 474-478, June.
    4. Chi Ma & Aparna H. Kesarwala & Tobias Eggert & José Medina-Echeverz & David E. Kleiner & Ping Jin & David F. Stroncek & Masaki Terabe & Veena Kapoor & Mei ElGindi & Miaojun Han & Angela M. Thornton & , 2016. "NAFLD causes selective CD4+ T lymphocyte loss and promotes hepatocarcinogenesis," Nature, Nature, vol. 531(7593), pages 253-257, March.
    5. David G. Bowen & Christopher M. Walker, 2005. "Adaptive immune responses in acute and chronic hepatitis C virus infection," Nature, Nature, vol. 436(7053), pages 946-952, August.
    6. Anita Gola & Michael G. Dorrington & Emily Speranza & Claudia Sala & Rochelle M. Shih & Andrea J. Radtke & Harikesh S. Wong & Antonio P. Baptista & Jonathan M. Hernandez & Gastone Castellani & Iain D., 2021. "Author Correction: Commensal-driven immune zonation of the liver promotes host defence," Nature, Nature, vol. 597(7874), pages 1-1, September.
    7. Anita Gola & Michael G. Dorrington & Emily Speranza & Claudia Sala & Rochelle M. Shih & Andrea J. Radtke & Harikesh S. Wong & Antonio P. Baptista & Jonathan M. Hernandez & Gastone Castellani & Iain D., 2021. "Commensal-driven immune zonation of the liver promotes host defence," Nature, Nature, vol. 589(7840), pages 131-136, January.
    8. Yusuke Nakanishi & Bao Lu & Craig Gerard & Akiko Iwasaki, 2009. "CD8+ T lymphocyte mobilization to virus-infected tissue requires CD4+ T-cell help," Nature, Nature, vol. 462(7272), pages 510-513, November.
    9. Stephen P. Schoenberger & Rene E. M. Toes & Ellen I. H. van der Voort & Rienk Offringa & Cornelis J. M. Melief, 1998. "T-cell help for cytotoxic T lymphocytes is mediated by CD40–CD40L interactions," Nature, Nature, vol. 393(6684), pages 480-483, June.
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