Johnson Aileen C, Karadkhele Geeta, Magua Wairimu, Vasanth Payas, Larsen Christian P
Department of Surgery, Emory University, Atlanta, GA.
Division of Nephrology, Department of Medicine, Emory University, Atlanta, GA.
Transplant Direct. 2022 May 26;8(6):e1339. doi: 10.1097/TXD.0000000000001339. eCollection 2022 Jun.
Cytopenias, a common complication for immunosuppressed patients, are known to be associated with adverse transplant outcomes. However, there is little information on cytopenias in recipients treated with the costimulation blockade agent, belatacept.
We compared cytopenia incidence and manifestations in patients undergoing kidney transplant at Emory University Hospital on tacrolimus and belatacept. To reduce selection bias, the tacrolimus group was narrowed to include only patients eligible for belatacept.
Of 1651 patients transplanted between 2009 and 2019, 187 (11%) experienced severe anemia, 309 (19%) experienced leukopenia, and 62 (4%) thrombocytopenia. On multivariable regressions, deceased-donor transplant, cytomegalovirus viremia, and thymoglobulin treatment were associated with risk of developing leukopenia, anemia, and thrombocytopenia. High-risk cytomegalovirus status was also associated with development of leukopenia and anemia. Additionally, azathioprine was associated with development of anemia, and both tacrolimus therapy and Caucasian race were associated with thrombocytopenia. Longitudinal quantifications of hematologic cell lines over the first-year posttransplant were extracted from generalized linear models fit using splines. Only hemoglobin range was significantly different between groups (greater in belatacept patients). Plots of mean cell count for each group suggest an earlier recovery from posttransplant anemia in belatacept patients.
Belatacept patients are not at increased risk of cytopenia but may have improved recovery from posttransplant anemia.
血细胞减少是免疫抑制患者的常见并发症,已知与移植不良结局相关。然而,关于接受共刺激阻断剂贝拉西普治疗的受者血细胞减少的信息很少。
我们比较了埃默里大学医院接受肾移植的患者使用他克莫司和贝拉西普时血细胞减少的发生率和表现。为了减少选择偏倚,将他克莫司组缩小到仅包括符合贝拉西普治疗条件的患者。
在2009年至2019年间接受移植的1651例患者中,187例(11%)出现严重贫血,309例(19%)出现白细胞减少,62例(4%)出现血小板减少。在多变量回归分析中,死亡供体移植、巨细胞病毒血症和抗胸腺细胞球蛋白治疗与白细胞减少、贫血和血小板减少的发生风险相关。高风险巨细胞病毒状态也与白细胞减少和贫血的发生相关。此外,硫唑嘌呤与贫血的发生相关,他克莫司治疗和白种人均与血小板减少相关。从使用样条拟合的广义线性模型中提取移植后第一年血液学细胞系的纵向定量数据。两组之间仅血红蛋白范围有显著差异(贝拉西普治疗的患者更高)。每组平均细胞计数图表明贝拉西普治疗的患者移植后贫血恢复较早。
接受贝拉西普治疗的患者血细胞减少风险并未增加,但移植后贫血的恢复可能有所改善。