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. 2020 Apr 15;13:36. doi: 10.1186/s13045-020-00863-9

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 8 — Hematoxylin and eosin staining in leukemia-infiltrated tissues after treatment with T22-GFP-H6-Auristatin. Hematoxylin and eosin staining of the liver, spleen, bone marrow, lung, pancreas, brain, heart, and kidneys of mice treated with vehicle (VEH) or T22-GFP-H6-Auristatin (T22-AUR) 14 days after the injection of CXCR4+ THP-1-Luci cells in NSG mice, compared with the stained tissues of a healthy mouse (Normal). T22-AUR, T22-GFP-H6-Auristatin group; VEH, vehicle group