Cited by 49Psoriasis: Treatment and PathogenesisT-cell and B-cell ImmunologyIL-33, ST2, and ILC Pathways

Induction of a colitogenic phenotype in Th1-like cells depends on interleukin-23 receptor signaling

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Pawlak, Mathias, DeTomaso, David, Schnell, Alexandra, Meyer zu Horste, Gerd, Lee, Youjin, Nyman, Jackson, Dionne, Danielle, Regan, Brianna M.L. +12 more·2022·Immunity

Abstract

Interleukin-23 receptor plays a critical role in inducing inflammation and autoimmunity. Here, we report that Th1-like cells differentiated in vitro with IL-12 + IL-21 showed similar IL-23R expression to that of pathogenic Th17 cells using eGFP reporter mice. Fate mapping established that these cells did not transition through a Th17 cell state prior to becoming Th1-like cells, and we observed their emergence in vivo in the T cell adoptive transfer colitis model. Using IL-23R-deficient Th1-like cells, we demonstrated that IL-23R was required for the development of a highly colitogenic phenotype. Single-cell RNA sequencing analysis of intestinal T cells identified IL-23R-dependent genes in Th1-like cells that differed from those expressed in Th17 cells. The perturbation of one of these regulators (CD160) in Th1-like cells inhibited the induction of colitis. We thus uncouple IL-23R as a purely Th17 cell-specific factor and implicate IL-23R signaling as a pathogenic driver in Th1-like cells inducing tissue inflammation.

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Crossref · 10.1016/j.immuni.2022.08.007

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Authors
Pawlak, M., DeTomaso, D., Schnell, A., Meyer zu Horste, G., Lee, Y., Nyman, J., Dionne, D., Regan, B. M. L., Singh, V., Delorey, T., Schramm, M. A., Wang, C., Wallrapp, A., Burkett, P. R., Riesenfeld, S. J., Anderson, A. C., Regev, A., Xavier, R. J., Yosef, N., & Kuchroo, V. K.
Affiliations
  • Broad Institute (US)
  • University of California, Berkeley (US)
  • Brigham and Women's Hospital (US)
  • Ragon Institute of MGH, MIT and Harvard (US)
Corresponding author
  • Xavier, Ramnik J.
  • Yosef, Nir
  • Kuchroo, Vijay K.
Venue
Immunity
Publisher
Elsevier BV
Published
2022-09
Volume
55
Issue
9
Pages
1663-1679.e6
ISSN
1074-7613 (ISSN-L)
OpenAlex
W4294770778
Cited by
49
References
93
Citations by year
2026: 10 · 2025: 12 · 2024: 16 · 2023: 8 · 2022: 3
FWCI
3.72
Type
journal article
Language
en
Open access
Locations
  • Immunity (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • NIH (1R01AI144166-01A1, 5P01AI039671-23, 5P01AI056299-17, 5P01AI073748-10)
  • National Multiple Sclerosis Society (TA-1605-08590)
  • Chan Zuckerberg Initiative
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
Keywords
IL23R, colitis, Th17 cells, CD160, intestinal T cells, adoptive T cell therapy, fate mapping, single-cell RNA sequencing, T cell differentiation
MeSH terms
Animals, Colitis, Inflammation, Mice, Inbred C57BL, Phenotype, Receptors, Interleukin, Th1 Cells, Mice, Interleukin-23, Th17 Cells

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