Kuczaj Agnieszka, Warwas Szymon, Zakliczyński Michał, Pawlak Szymon, Przybyłowski Piotr, Śliwka Joanna, Hrapkowicz Tomasz
Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland; Silesian Center for Heart Diseases, 41-800 Zabrze, Poland.
Students' Scientific Association affiliated with the Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.
Transpl Immunol. 2023 Dec;81:101937. doi: 10.1016/j.trim.2023.101937. Epub 2023 Sep 29.
The study aimed to determine the influence of induction therapy on the acute cellular rejection (ACR) index in adult heart transplant recipients during the one-year observation. The study population consisted of 256 consecutive adult patients (pts), aged 51.5 (±11.9) years, 199 (77%) men treated with orthotopic heart transplantation (OHT) in the period between 2015 and 2020 in a single high-volume heart transplant center. The endomyocardial biopsies (EMBs) were performed according to the protocol consisting of 7 protocolary EMBs for up to 3 months and 10 EMBs for up to one year after OHT. The rejection index (ACRI) was calculated as the number of scheduled EMBs with the ACR ≥ 2 divided by the total number of protocolary EMBs. The study population was divided into two groups according to the application of basiliximab. The total number of pts. who received basiliximab was 10 (3.9%). The main indications for the usage of the induction therapy were heart retransplantation, mechanical circulatory support (MCS), severe renal insufficiency (eGFR <30 mL/min/1.73 m2), and a panel of reactive antibody (PRA) > 10%. In the group with induction, the mean age was 49 (±14) years; 3 (30%) patients had the MCS prior to OHT, and 3 (30%) patients had heart retransplantation. Four (40%) patients had diabetes mellitus, and 4 (40%) patients had severe renal insufficiency. As maintenance therapy during the observation period, tacrolimus was given to 10 (100%) patients, everolimus to 2 (20%) patients, and MPA to 9 (90%) patients. In the group with no induction, the mean age was 51.8 (±12) years, MCS was used in 56 (23%) patients, 2 (0.8%) patients were retransplanted; 10 (4%) patients had eGFR <30 mL/min/1.73 m2 and 58 (24%) patients had diabetes. Tacrolimus was administered to 243 (99%) patients, cyclosporine to 3 (1%), everolimus to 40 (16%), and mycophenolate to 245 (99.6%) heart recipients. The median one-year ACRI was 0.0, IQR:0.0-0.08 in the group with induction vs. 0.077, IQR: 0.0-0.154 with no induction; p = 0.11. ACRI up to three months was significantly higher in the entire cohort in comparison to up to one year (P < 0.01). The multivariate analysis showed that only everolimus implementation and younger age at the time of transplant influenced patients' mortality rate (P < 0.01). Significant graft rejections (≥ 2R ISHLT) are most common in the first three months after OHT. Patients who are initially at high risk of significant cellular rejection may benefit from induction therapy.
该研究旨在确定诱导治疗对成年心脏移植受者在一年观察期内急性细胞排斥反应(ACR)指数的影响。研究人群包括256例连续的成年患者,年龄为51.5(±11.9)岁,其中199例(77%)为男性,于2015年至2020年期间在一家大型心脏移植中心接受原位心脏移植(OHT)。心肌内膜活检(EMB)按照方案进行,在OHT后3个月内进行7次方案规定的EMB,1年内进行10次EMB。排斥反应指数(ACRI)的计算方法为ACR≥2的计划EMB次数除以方案规定的EMB总数。根据巴利昔单抗的应用情况,将研究人群分为两组。接受巴利昔单抗治疗的患者总数为10例(3.9%)。诱导治疗的主要适应证为心脏再次移植、机械循环支持(MCS)、严重肾功能不全(估算肾小球滤过率<30 mL/min/1.73 m²)以及群体反应性抗体(PRA)>10%。在诱导治疗组中,平均年龄为49(±14)岁;3例(30%)患者在OHT前接受了MCS,3例(30%)患者进行了心脏再次移植。4例(40%)患者患有糖尿病,4例(40%)患者患有严重肾功能不全。在观察期内,作为维持治疗,10例(100%)患者使用了他克莫司,2例(20%)患者使用了依维莫司,9例(90%)患者使用了霉酚酸酯。在无诱导治疗组中,平均年龄为51.8(±12)岁,56例(23%)患者使用了MCS,2例(0.8%)患者进行了再次移植;10例(4%)患者的估算肾小球滤过率<30 mL/min/1.73 m²,58例(24%)患者患有糖尿病。243例(99%)心脏受者使用了他克莫司,3例(1%)使用了环孢素,40例(16%)使用了依维莫司,245例(99.6%)使用了霉酚酸。诱导治疗组的一年ACRI中位数为0.0,四分位数间距为0.0 - 0.08;无诱导治疗组为0.077,四分位数间距为0.0 - 0.154;p = 0.11。与一年时相比,整个队列在3个月时的ACRI显著更高(P < 0.01)。多变量分析显示,只有依维莫司的使用和移植时年龄较小会影响患者的死亡率(P < 0.01)。严重的移植排斥反应(≥2R ISHLT)在OHT后的前三个月最为常见。最初有显著细胞排斥反应高风险的患者可能从诱导治疗中获益。