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. 2023 Feb 27;11:11. doi: 10.1038/s41413-023-00246-z

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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. 6 — The main process used to generate ex vivo DC vaccines. Progenitor cells are extracted from patients via dialysis, induced to transition into mature DCs, and then loaded with tumor antigens for administration to patients. Tumor antigen-specific T lymphocytes are activated by injected antigen-loaded DCs to exert an antitumor effect