cDC1-derived IL-27 regulates small intestinal CD4+ T cell homeostasis in mice

Author:

Ahmadi Fatemeh1ORCID,Junghus Fredrik2ORCID,Ashworth Christian1ORCID,Lappalainen Amanda1ORCID,Mörbe Urs2ORCID,Kotarsky Knut1ORCID,Agace William W.12ORCID

Affiliation:

1. Immunology Section, Department of Experimental Medicine, Lund University, Lund, Sweden 1

2. Mucosal Immunology Group, Department of Health Technology, Technical University of Denmark, Lyngby, Denmark 2

Abstract

The small intestinal lamina propria contains large numbers of IFNγ-producing T helper (Th1) cells that play important roles in intestinal homeostasis and host defense, but the mechanisms underlying their development remain poorly understood. Here, we demonstrate that Th1 cells accumulate in the SI-LP after weaning and are maintained there long term. While both Th17 and Th1 cell accumulation in the SI-LP was microbiota dependent, Th1 cell accumulation uniquely required IL-27 and MHCII expression by cDC1. This reflected a requirement for IL-27 signaling in the priming of Th1 cells rather than for their maintenance once in the mucosa. cDC1-derived IL-27 was essential for maintaining the Th1–Th17 balance within the SI-LP, and in its absence, remaining Th1 cells expressed enhanced levels of Th17 signature genes. In conclusion, we identify cDC1-derived IL-27 as a key regulator of SI-LP Th1–Th17 cell homeostasis.

Funder

Swedish Research Council

Knut and Alice Wallenberg Foundation

Swedish Cancerfonden

Danish Research Council

Lundbeck Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference55 articles.

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