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. 2019 Oct 25;51(10):126. doi: 10.1038/s12276-019-0329-9

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© The Author(s) 2019

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. 6 — CD1d^WT OT-1 CD8⁺ T cells or CD1d^KO OT-1 CD8⁺ T cells were intravenously transferred to wild type (a) and Jα18^KO NKT cell-deficient (b) mice (n = 5). Tumor growth was monitored every 2–4 days. The data shown are representative of two independent experiments with similar results. Data are presented as the mean ± SEM. **p < 0.01, ***p < 0.001; two-way ANOVA with Bonferroni’s multiple comparison test