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

被引:14
|
作者
Leal, Rita [1 ,2 ,3 ]
Tsapepas, Demetra [4 ]
Crew, Russell J. [5 ]
Dube, Geoffrey K. [5 ]
Ratner, Lloyd [6 ]
Batal, Ibrahim [3 ]
机构
[1] Ctr Hosp Coimbra, Dept Nephrol, Coimbra, Portugal
[2] Univ Coimbra, Coimbra, Portugal
[3] Columbia Univ Coll Phys & Surg, Dept Pathol & Cell Biol, 630 W 168th St,VC 14-238, New York, NY 10032 USA
[4] NewYork Presbyterian Hosp, Dept Pharm, New York, NY USA
[5] Columbia Univ Coll Phys & Surg, Dept Med, Div Nephrol, New York, NY USA
[6] Columbia Univ Coll Phys & Surg, Dept Surg, Div Transplantat, New York, NY 10032 USA
来源
KIDNEY INTERNATIONAL REPORTS | 2018年 / 3卷 / 02期
关键词
calcineurin inhibitors; drug toxicity; kidney transplantation; mammalian target of rapamycin; transplant pathology; NOVO THROMBOTIC MICROANGIOPATHY; CYCLOSPORINE NEPHROTOXICITY; INTERSTITIAL FIBROSIS; ALLOGRAFT-REJECTION; OXIDATIVE STRESS; SIROLIMUS; EXPRESSION; RECIPIENTS; MTOR; IMMUNOSUPPRESSION;
D O I
10.1016/j.ekir.2017.10.010
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:281 / 290
页数:10
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