Department of General Surgery, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, China.
Xenotransplantation Program, Department of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Am J Transplant. 2020 Apr;20(4):999-1013. doi: 10.1111/ajt.15712. Epub 2020 Jan 3.
The interleukin (IL)-6/IL-6 receptor-α (IL-6Rα)/signal transduction and activation of the transcription 3 (STAT3) pathway plays an important role in inflammation. Anti-human IL-6Rα blockade by tocilizumab (TCZ) has been used in pig-to-baboon organ xenotransplant models, but whether it is beneficial remains uncertain. After xenotransplant, there were significant increases in both baboon and pig IL-6 in the baboon serum, especially in baboons that received TCZ before xenotransplant. In vitro observations demonstrated that human, baboon, and pig IL-6 can activate the IL-6/IL-6Rα/STAT3 pathway in human, baboon, and pig cells, respectively. Activation of the IL-6/IL-6Rα/STAT3 pathway was blocked by TCZ in human and baboon cells but not in pig cells (ie, pig IL-6R). Siltuximab (human IL-6 inhibitor) bound to both human and baboon, but not pig, IL-6 and suppressed activation of the IL-6/IL-6Rα/STAT3 pathway. These results indicate that TCZ and siltuximab do not cross-react with pig IL-6R and pig IL-6, respectively. Rapamycin partially inhibited human, baboon, and pig IL-6/IL-6Rα/STAT3 pathways and suppressed inflammatory gene expression. TCZ treatment increased serum IL-6 because it could no longer bind to baboon IL-6Rα. We suggest that increased serum IL-6 may be detrimental to the pig xenograft because it is likely to bind to pig IL-6R, resulting in activation of pig cells.
白细胞介素 (IL)-6/IL-6 受体-α (IL-6Rα)/信号转导和转录激活因子 3 (STAT3) 通路在炎症中发挥重要作用。托珠单抗 (TCZ) 抗人 IL-6Rα 阻断已用于猪到狒狒器官异种移植模型,但是否有益尚不确定。异种移植后,狒狒和猪血清中的 IL-6 均显著增加,尤其是在异种移植前接受 TCZ 的狒狒。体外观察表明,人、狒狒和猪 IL-6 可分别激活人、狒狒和猪细胞中的 IL-6/IL-6Rα/STAT3 通路。TCZ 可阻断人、狒狒细胞中的 IL-6/IL-6Rα/STAT3 通路,但不能阻断猪细胞中的通路(即猪 IL-6R)。西妥昔单抗(人 IL-6 抑制剂)与人、狒狒结合,但不与猪结合,抑制 IL-6/IL-6Rα/STAT3 通路的激活。这些结果表明 TCZ 和西妥昔单抗分别不与猪 IL-6R 和猪 IL-6 发生交叉反应。雷帕霉素部分抑制人、狒狒和猪的 IL-6/IL-6Rα/STAT3 通路并抑制炎症基因表达。TCZ 治疗增加了血清 IL-6,因为它不能再与狒狒 IL-6Rα 结合。我们认为,血清 IL-6 的增加可能对猪异种移植物有害,因为它可能与猪 IL-6R 结合,导致猪细胞激活。