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. 2020 Feb 18;122(8):1185–1193. doi: 10.1038/s41416-020-0757-2

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© The Author(s) 2020

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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Fig. 3 — a C57B/6 J mice were immunised with the indicated concentrations of XCL1-OT-I with or without 20 µg of poly(I:C). b Wild-type or XCR1-deficient (Xcr1^venus/venus, open circles) mice were immunised with 2 µg of XCL1-OT-I plus 20 µg of poly(I:C). Seven days after immunisation, splenocytes were stimulated with OT-I peptide and analysed by a flow cytometer. Percentages of IFN-γ-producing CD62L⁻ cells in CD8⁺ T cells are shown. The results of three independent experiments were combined. *p < 0.05, with Mann–Whitney U test.