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. 2023 Mar 7;6:245. doi: 10.1038/s42003-023-04615-6

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© The Author(s) 2023

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. 7 — CHO_EV and CHO_CD47 cells were either untreated or irradiated and were allowed to rest for 6 h. Then, cells were co-cultured with PBMCs. After 72 h, conditioned media were collected and analyzed for IFNγ secretion. The level of IFNγ secreted by PBMC cultured in the absence or presence of the CHO cells, is presented. Graph shows an average (± STD) of triplicate samples in each group. Representative of three experiments using three independent blood donors is shown.