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. 2020 Apr 23;34(12):3310–3322. doi: 10.1038/s41375-020-0828-7

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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. 2 — a Of the ten tumor-associated antigens, T-cell responses against MAGE-C1 and MAGE-A3 were significantly increased in patient peripheral blood mononuclear cell samples after measles virus-sodium iodide symporter (MV-NIS) virotherapy. (n = 10). Gray-shaded area denotes the limit of negative response. b Representative image showing increased IFN-γ responses against MAGE-C1, MAGE-A1, and MUC-1 at 6 weeks after MV-NIS virotherapy. CEF peptide pool was used as a positive control. Sole asterisk indicates P < 0.05, double asterisks, P < 0.01; triple asterisks, P < 0.001, compared with the corresponding groups. Error bars indicate mean with standard error of mean. CEF indicates CEF-positive control peptide pools; CT/DMSO control/dimethylsulfoxide, IFN interferon.