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. 2022 Sep 7;610(7933):752–760. doi: 10.1038/s41586-022-05309-5

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 10 — a, Gating strategy for identification of ILC3 and TC subsets in mLN of Itgb8^tdTomato mice at P14 (representative of n = 4 mice, three independent experiments). b, Itgb8 transcript levels in TC and ILC3 subsets profiled by Smart-seq 2. c, Chromatin accessibility at the Itgb8 locus and Itgb8 transcript levels in TC and ILC3 subsets (cells as in Fig 1c). d. Frequency of total Foxp3⁺ Treg cells and percentage of RORγt⁺ pTreg cells in mLN and LI of Itgb8^ΔCd4 (n = 8) or Itgb8^fl/fl mice (n = 7). Data pooled from two (d) or 3 (a) independent experiments. Error bars: means ± s.e.m. NS, not significant; unpaired two-sided t-test.

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