Leon H. Charney Division of Cardiology, New York University Grossman School of Medicine, New York, New York, USA.
Department of Pathology, New York University Grossman School of Medicine, New York, New York, USA.
Clin Transplant. 2022 Jul;36(7):e14745. doi: 10.1111/ctr.14745. Epub 2022 Jun 22.
ImmuKnow, an immune cell function assay that quantifies overall immune system activity can assist in post-transplant immunosuppression adjustment. However, the utility of pre-transplant ImmuKnow results representing a patient's baseline immune system activity is unknown. This study sought to assess if pre-transplant ImmuKnow results are predictive of rejection at the time of first biopsy in our cardiac transplant population.
This is a single center, retrospective observational study of consecutive patients from January 1, 2018 to October 1, 2020 who underwent orthotopic cardiac transplantation at NYU Langone Health. Patients were excluded if a pre-transplant ImmuKnow assay was not performed. ImmuKnow results were categorized according to clinical interpretation ranges (low, moderate, and high activity), and patients were divided into two groups: a low activity group versus a combined moderate-high activity group. Pre-transplant clinical characteristics, induction immunosuppression use, early postoperative tacrolimus levels, and first endomyocardial biopsy results were collected for all patients. Rates of clinically significant early rejection (defined as rejection ≥ 1R/1B) were compared between pre-transplant ImmuKnow groups.
Of 110 patients who underwent cardiac transplant, 81 had pre-transplant ImmuKnow results. The low ImmuKnow activity group was comprised of 15 patients, and 66 patients were in the combined moderate-high group. Baseline characteristics were similar between groups. Early rejection occurred in 0 (0%) patients with low pre-transplant ImmuKnow levels. Among the moderate- high pre-transplant ImmuKnow group, 16 (24.2%) patients experienced early rejection (P = .033). The mean ImmuKnow level in the non-rejection group was the 364.9 ng/ml of ATP compared to 499.3 ng/ml of ATP for those with rejection (P = .020).
Patients with low pre-transplant ImmuKnow levels had lower risk of early rejection when compared with patients with moderate or high levels. Our study suggests a possible utility in performing pre-transplant ImmuKnow to identify patients at-risk for early rejection who may benefit from intensified upfront immunosuppression as well as to recognize those where slower calcineurin inhibitor initiation may be appropriate.
ImmuKnow 是一种能够量化整体免疫系统活性的免疫细胞功能检测方法,可辅助移植后免疫抑制剂的调整。然而,移植前 ImmuKnow 结果是否能代表患者的基础免疫系统活性尚不清楚。本研究旨在评估我们心脏移植患者中,移植前 ImmuKnow 结果是否可预测首次活检时的排斥反应。
这是一项在 2018 年 1 月 1 日至 2020 年 10 月 1 日期间于纽约大学朗格尼健康中心接受原位心脏移植的连续患者的单中心回顾性观察性研究。如果未进行移植前 ImmuKnow 检测,则排除患者。根据临床解释范围(低、中、高活性)对 ImmuKnow 结果进行分类,并将患者分为低活性组和中-高活性混合组。收集所有患者的移植前临床特征、诱导免疫抑制使用、术后早期他克莫司水平和首次心内膜心肌活检结果。比较移植前 ImmuKnow 组之间临床显著早期排斥(定义为排斥反应≥1R/1B)的发生率。
在 110 例接受心脏移植的患者中,81 例有移植前 ImmuKnow 结果。低 ImmuKnow 活性组有 15 例患者,中-高活性组有 66 例患者。两组间基线特征相似。低移植前 ImmuKnow 水平组的患者无一例发生早期排斥反应(0%)。在中-高移植前 ImmuKnow 组中,有 16 例(24.2%)患者发生早期排斥反应(P=0.033)。无排斥反应组的平均 ImmuKnow 水平为 364.9ng/ml ATP,而发生排斥反应组为 499.3ng/ml ATP(P=0.020)。
与中-高水平组相比,移植前 ImmuKnow 水平较低的患者发生早期排斥反应的风险较低。本研究表明,移植前进行 ImmuKnow 检测可能具有一定的效用,可识别发生早期排斥反应风险较高的患者,这些患者可能需要强化初始免疫抑制治疗,也可识别那些可能需要更缓慢开始钙调神经磷酸酶抑制剂治疗的患者。