The emerging family of RORγt+ antigen-presenting cells

Jakub Abramson*, Jan Dobeš, Mengze Lyu, Gregory F. Sonnenberg*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

15 Citations (Scopus)

Abstract

Antigen-presenting cells (APCs) are master regulators of the immune response by directly interacting with T cells to orchestrate distinct functional outcomes. Several types of professional APC exist, including conventional dendritic cells, B cells and macrophages, and numerous other cell types have non-classical roles in antigen presentation, such as thymic epithelial cells, endothelial cells and granulocytes. Accumulating evidence indicates the presence of a new family of APCs marked by the lineage-specifying transcription factor retinoic acid receptor-related orphan receptor-γt (RORγt) and demonstrates that these APCs have key roles in shaping immunity, inflammation and tolerance, particularly in the context of host–microorganism interactions. These RORγt+ APCs include subsets of group 3 innate lymphoid cells, extrathymic autoimmune regulator-expressing cells and, potentially, other emerging populations. Here, we summarize the major findings that led to the discovery of these RORγt+ APCs and their associated functions. We discuss discordance in recent reports and identify gaps in our knowledge in this burgeoning field, which has tremendous potential to advance our understanding of fundamental immune concepts.

Original languageEnglish
Pages (from-to)64-77
Number of pages14
JournalNature Reviews Immunology
Volume24
Early online dateJul 2023
DOIs
Publication statusPublished - Jan 2024

Bibliographical note

Funding Information:
The authors thank members of the Abramson, Dobeš and Sonnenberg laboratories for discussions and critical reading of the manuscript. G.F.S. is kindly supported by the National Institutes of Health (R01AI143842, R01AI123368, R01AI145989, U01AI095608, R01AI162936, R37AI174468 and R01CA274534), the NIAID Mucosal Immunology Studies Team (MIST), an Investigators in the Pathogenesis of Infectious Disease Award from the Burroughs Wellcome Fund, the Cancer Research Institute, Linda and Glenn Greenberg, the Dalton Family Foundation, and the Roberts Institute for Research in IBD. G.F.S. is a CRI Lloyd J. Old STAR. M.L. is supported by a Crohn’s and Colitis Foundation Research Fellowship Award (#935259). J.A. is kindly supported by the Eugene and Marcia Applebaum Professorial Chair, European Research Council (ERC-2016-CoG-724821), IOCB fellowship for sabbatical visit program (RVO 61388963) and Bill and Marika Glied and Family Fund. J.D. is kindly supported by the Czech Science Foundation JUNIOR STAR grant (21-22435M), Czech Science Foundation grant (22-30879S) and by the Charles University PRIMUS grant (Primus/21/MED/003).

Publisher Copyright:
© 2023, Springer Nature Limited.

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology

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