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. 2019 Feb 4;9:1225. doi: 10.1038/s41598-018-37883-y

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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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YOVAL1.1 tumors are responsive to immune checkpoint blockade in vivo. (a,b) Response of YUMM1.1 (a) and YOVAL1.1 (b) tumors to immunotherapy. Tumor growth and survival in response to combination anti-PD-1 and anti-CTLA-4 or isotype controls in C57BL/6 mice, n = 10–12. (c,d) YOVAL1.1 tumor growth in response to anti-PD-1 (c) or anti-CTLA-4 (d) or isotype controls. (a–d) Survival measured as time for tumors to reach >1200 mm³, arrows indicate treatment days. ns – not significant, Log-rank (Mantel-Cox) test, error bars show ±SEM. ****p < 0.0001.