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肾移植中钙调神经磷酸酶和雷帕霉素哺乳动物靶蛋白抑制剂的病理学

Pathology of Calcineurin and Mammalian Target of Rapamycin Inhibitors in Kidney Transplantation.

作者信息

Leal Rita, Tsapepas Demetra, Crew Russell J, Dube Geoffrey K, Ratner Lloyd, Batal Ibrahim

机构信息

Department of Nephrology, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.

Department of Pathology and Cell Biology, Columbia University, College of Physicians and Surgeons, New York, New York, USA.

出版信息

Kidney Int Rep. 2017 Oct 27;3(2):281-290. doi: 10.1016/j.ekir.2017.10.010. eCollection 2018 Mar.

DOI:10.1016/j.ekir.2017.10.010
PMID:30276344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6161639/
Abstract

The recent evolution in immunosuppression therapy has led to significant improvement in short-term kidney allograft outcomes; however, this progress did not translate into similar improvement in long-term graft survival. The latter, at least in part, is likely to be attributed to immunosuppressant side effects. In this review, we focus on the histologic manifestations of calcineurin inhibitor and mammalian target of rapamycin inhibitor toxicity. We discuss the pathologic features attributed to such toxicity and allude to the lack of highly specific pathognomonic lesions. Finally, we highlight the importance of clinicopathologic correlation to achieve a meaningful pathologic interpretation.

摘要

免疫抑制疗法的最新进展已使短期肾移植结果有了显著改善;然而,这一进展并未转化为长期移植肾存活的类似改善。长期移植肾存活至少部分可能归因于免疫抑制剂的副作用。在本综述中,我们重点关注钙调神经磷酸酶抑制剂和雷帕霉素靶蛋白抑制剂毒性的组织学表现。我们讨论了归因于此类毒性的病理特征,并提及缺乏高度特异性的特征性病变。最后,我们强调临床病理相关性对于获得有意义的病理解释的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/299fca75aecc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/b4df9447afcb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/ce32c6630349/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/1cd7aa49936e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/856f6a755311/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/299fca75aecc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/b4df9447afcb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/ce32c6630349/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/1cd7aa49936e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/856f6a755311/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79a/6161639/299fca75aecc/gr5.jpg

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Transplant Rev (Orlando). 2017 Jan;31(1):10-17. doi: 10.1016/j.trre.2016.10.006. Epub 2016 Oct 11.
2
Influence of tacrolimus metabolism rate on renal function after solid organ transplantation.他克莫司代谢率对实体器官移植后肾功能的影响。
World J Transplant. 2017 Feb 24;7(1):26-33. doi: 10.5500/wjt.v7.i1.26.
3
Targeting mTOR Signaling Can Prevent the Progression of FSGS.靶向雷帕霉素靶蛋白信号传导可预防局灶节段性肾小球硬化的进展。
个体化营养干预对肾移植受者肾功能、身体成分和生活质量的影响:一项随机临床试验研究方案。
PLoS One. 2022 Aug 4;17(8):e0272484. doi: 10.1371/journal.pone.0272484. eCollection 2022.
4
Three-Year Outcomes in Kidney Transplant Recipients Switched From Calcineurin Inhibitor-Based Regimens to Belatacept as a Rescue Therapy.钙调磷酸酶抑制剂方案转换为贝利尤单抗作为挽救治疗的肾移植受者 3 年结局。
Transpl Int. 2022 Apr 13;35:10228. doi: 10.3389/ti.2022.10228. eCollection 2022.
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Case Report: Collapsing Focal Segmental Glomerulosclerosis After Initiation of Ado-Trastuzumab Emtansine Therapy.病例报告:阿多曲妥珠单抗(ado - 曲妥珠单抗)治疗开始后出现的塌陷型局灶节段性肾小球硬化症
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