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白细胞介素-6 受体阻断(托珠单抗)对猪-狒狒器官异种移植有益还是有害?

Is interleukin-6 receptor blockade (tocilizumab) beneficial or detrimental to pig-to-baboon organ xenotransplantation?

机构信息

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.

出版信息

Am J Transplant. 2020 Apr;20(4):999-1013. doi: 10.1111/ajt.15712. Epub 2020 Jan 3.

Abstract

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.

摘要

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。

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