Kidney Allograft Survival After Acute Rejection, the Value of Follow-Up Biopsies

被引:134
作者
El Ters, M. [1 ]
Grande, J. P. [2 ]
Keddis, M. T. [1 ]
Rodrigo, E.
Chopra, B. [1 ,3 ]
Dean, P. G. [3 ,4 ]
Stegall, M. D. [3 ,4 ]
Cosio, F. G. [1 ,3 ]
机构
[1] Mayo Clin, Div Nephrol & Hypertens, Rochester, MN USA
[2] Mayo Clin, Dept Pathol, Rochester, MN USA
[3] Mayo Clin, William von Liebig Transplant Ctr, Rochester, MN USA
[4] Mayo Clin, Dept Surg & Transplant Ctr, Rochester, MN USA
关键词
Acute rejection; graft histology; graft survival; protocol biopsies; ANTIBODY-MEDIATED REJECTION; CHRONIC HUMORAL REJECTION; TRANSPLANT GLOMERULOPATHY; MYCOPHENOLATE-MOFETIL; SUBCLINICAL REJECTION; PROTOCOL BIOPSIES; HEPATITIS-C; RISK-FACTOR; INFLAMMATION; RECIPIENTS;
D O I
10.1111/ajt.12370
中图分类号
R61 [外科手术学];
学科分类号
摘要
Kidney allografts are frequently lost due to alloimmunity. Still, the impact of early acute rejection (AR) on long-term graft survival is debated. We examined this relationship focusing on graft histology post-AR and assessing specific causes of graft loss. Included are 797 recipients without anti-donor antibodies (DSA) at transplant who had 1 year protocol biopsies. 15.2% of recipients had AR diagnosed by protocol or clinical biopsies. Compared to no-AR, all histologic types of AR led to abnormal histology in 1 and 2 years protocol biopsies, including more fibrosis+inflammation (6.3% vs. 21.9%), moderate/severe fibrosis (7.7% vs. 13.5%) and transplant glomerulopathy (1.4% vs. 8.3%, all p<0.0001). AR were associated with reduced graft survival (HR=3.07 (1.92-4.94), p<0.0001). However, only those AR episodes followed by abnormal histology led to reduced graft survival. Early AR related to more late alloimmune-mediated graft losses, particularly transplant glomerulopathy (31% of losses). Related to this outcome, recipients with AR were more likely to have new DSA class II 1 year posttransplant (no-AR, 11.1%; AR, 21.2%, p=0.039). In DSA negative recipients, early AR often leads to persistent graft inflammation and increases the risk of new DSA II production. Both of these post-AR events are associated with increased risk of graft loss.
引用
收藏
页码:2334 / 2341
页数:8
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