Significance of revised criteria for chronic active T cell-mediated rejection in the 2017 Banff classification: Surveillance by 1-year protocol biopsies for kidney transplantation

Significance of revised criteria for chronic active T cell-mediated rejection in the 2017 Banff classification: Surveillance by 1-year protocol biopsies for kidney transplantation
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DOI:
10.1111/ajt.16093
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发表时间:
2021-01-01
影响因子:
8.8
通讯作者:
Kitazono, Takanari
Kitazono, Takanari
中科院分区:
医学2区
文献类型:
--
作者:
Nakagawa, Kaneyasu;Tsuchimoto, Akihiro;Kitazono, Takanari

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慢性活动性T细胞介导的排斥反应(CA-TCMR)的诊断标准在Banff 2017共识中进行了修订,但尚不清楚新标准是否能预测肾移植的移植物预后。我们入组了406例接受1年方案活检(PB)的肾移植受者,并研究了Banff 2017的诊断意义。3位诊断医生的观察者间重复性显示Fleiss kappa系数的基本一致率为0.68。根据Banff 2017,33例患者(8%)被归类为CA-TCMR,根据Banff 2015标准,6例既往诊断为正常,12例为急性TCMR,10例为临界变化,5例为CA-TCMR。CA-TCMR的决定性因素是环孢霉素的使用(与他克莫司相比)、既往急性排斥反应和BK多瘤病毒相关肾病。在生存分析中,CA-TCMR的新诊断预测了复合移植终点,定义为血清肌酐加倍或死亡删失的移植物丢失(对数秩检验,P < .001)。在多变量分析中,CA-TCMR与复合终点的第二高风险相关(风险比:5.42; 95%置信区间,2.02-14.61; P < .001 vs正常),仅次于抗体介导的排斥反应。总之,Banff 2017中CA-TCMR的诊断可能有助于检测接受1年PB的肾移植受者的不良预后。
Diagnostic criteria for chronic active T cell-mediated rejection (CA-TCMR) were revised in the Banff 2017 consensus, but it is unknown whether the new criteria predict graft prognosis of kidney transplantation. We enrolled 406 kidney allograft recipients who underwent a 1-year protocol biopsy (PB) and investigated the diagnostic significance of Banff 2017. Interobserver reproducibility of the 3 diagnosticians showed a substantial agreement rate of 0.68 in Fleiss's kappa coefficient. Thirty-three patients (8%) were classified as CA-TCMR according to Banff 2017, and 6 were previously diagnosed as normal, 12 as acute TCMR, 10 with borderline changes, and 5 as CA-TCMR according to Banff 2015 criteria. Determinant factors of CA-TCMR were cyclosporine use (vs tacrolimus), previous acute rejection, and BK polyomavirus-associated nephropathy. In survival analysis, the new diagnosis of CA-TCMR predicted a composite graft endpoint defined as doubling serum creatinine or death-censored graft loss (log-rank test, P < .001). In multivariate analysis, CA-TCMR was associated with the second highest risk of the composite endpoint (hazard ratio: 5.42; 95% confidence interval, 2.02-14.61; P < .001 vs normal) behind antibody-mediated rejection. In conclusion, diagnosis of CA-TCMR in Banff 2017 may facilitate detecting an unfavorable prognosis of kidney allograft recipients who undergo a 1-year PB.