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. 2022 Jun 15;22(10):2306–2322. doi: 10.1111/ajt.17116

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© 2022 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

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Ischemia reperfusion injury, MCMV infection, and allogeneic transplantation each contribute to intragraft Th17 cell infiltration. (A) Syngeneic transplantation was performed using D−R− and D+R+ grafts to evaluate role of ischemia–reperfusion injury (IRI) without alloimmune responses. (B) CCL20 and CXCL10 quantities in D−R− and D+R+ syngeneic transplants. (C) Frequencies of Th17 infiltrates in syngeneic D−R− and D+R+ grafts. (D) Intragraft Th17 cells co‐expressing IFN‐γ and/or TNF‐α in D−R− and D+R+ grafts. (E) Percentage and proportions of single or multiple cytokines expressing Th17 cells in syngeneic and allogeneic grafts. For (A–D), data are represented as mean ± standard deviation (SD) and are analyzed by two‐sided Student's t‐test. For (E), mean values are shown.