cDC1 prime and are licensed by CD4+ T cells to induce anti-tumour immunity

• Published in: Nature (London) Vol. 584; no. 7822; pp. 624 - 629
• Main Authors: Ferris, Stephen T., Durai, Vivek, Wu, Renee, Theisen, Derek J., Ward, Jeffrey P., Bern, Michael D., Davidson, Jesse T., Bagadia, Prachi, Liu, Tiantian, Briseño, Carlos G., Li, Lijin, Gillanders, William E., Wu, Gregory F., Yokoyama, Wayne M., Murphy, Theresa L., Schreiber, Robert D., Murphy, Kenneth M.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 27.08.2020; Nature Publishing Group
• Subjects: 13/31; 38/39; 45/61; 631/250/262; 631/250/580; 64/60; Animals; Antigen presentation; Antigen Presentation - immunology; Antigen processing; Antigens; CD4 antigen; CD4-Positive T-Lymphocytes - cytology; CD4-Positive T-Lymphocytes - immunology; CD40 antigen; CD40 Antigens - immunology; CD40 Antigens - metabolism; CD8 antigen; CD8-Positive T-Lymphocytes - immunology; Cdc2 protein; Cell activation; Cell division; Cell growth; Cell interactions; Clonal deletion; Cross-Priming; Crosstalk; Deletion; Dendritic cells; Dendritic Cells - cytology; Dendritic Cells - immunology; Dendritic Cells - metabolism; Female; Fibrosarcoma; Histocompatibility; Histocompatibility Antigens Class II - immunology; Humanities and Social Sciences; Immunity; Lymph nodes; Lymphatic system; Lymphocytes; Lymphocytes T; Mice; multidisciplinary; Neoplasms - immunology; Priming; Rejection; Science; Science (multidisciplinary); Signal Transduction; Signaling; Tumors
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/s41586-020-2611-3

Conventional type 1 dendritic cells (cDC1) 1 are thought to perform antigen cross-presentation, which is required to prime CD8 + T cells 2 , 3 , whereas cDC2 are specialized for priming CD4 + T cells 4 , 5 . CD4 + T cells are also considered to help CD8 + T cell responses through a variety of mechanisms 6 – 11 , including a process whereby CD4 + T cells ‘license’ cDC1 for CD8 + T cell priming 12 . However, this model has not been directly tested in vivo or in the setting of help-dependent tumour rejection. Here we generated an Xcr1 Cre mouse strain to evaluate the cellular interactions that mediate tumour rejection in a model requiring CD4 + and CD8 + T cells. As expected, tumour rejection required cDC1 and CD8 + T cell priming required the expression of major histocompatibility class I molecules by cDC1. Unexpectedly, early priming of CD4 + T cells against tumour-derived antigens also required cDC1, and this was not simply because they transport antigens to lymph nodes for processing by cDC2, as selective deletion of major histocompatibility class II molecules in cDC1 also prevented early CD4 + T cell priming. Furthermore, deletion of either major histocompatibility class II or CD40 in cDC1 impaired tumour rejection, consistent with a role for cognate CD4 + T cell interactions and CD40 signalling in cDC1 licensing. Finally, CD40 signalling in cDC1 was critical not only for CD8 + T cell priming, but also for initial CD4 + T cell activation. Thus, in the setting of tumour-derived antigens, cDC1 function as an autonomous platform capable of antigen processing and priming for both CD4 + and CD8 + T cells and of the direct orchestration of their cross-talk that is required for optimal anti-tumour immunity. Conventional type 1 dendritic cells perform antigen processing and priming of CD4 + and CD8 + T cells against tumour antigens, orchestrating their cross-talk to effect anti-tumour immunity.