Department of Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.
Department of Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.
Hepatobiliary Pancreat Dis Int. 2017 Oct 15;16(5):487-492. doi: 10.1016/S1499-3872(17)60050-X.
The manipulation of immunosuppression therapy remains challenging in patients who develop infectious diseases or multiple organ dysfunction after liver transplantation. We evaluated the outcomes of delayed introduction of immunosuppression in the patients after liver transplantation under immune monitoring with ImmuKnow assay.
From March 2009 to February 2014, 225 consecutive liver recipients in our institute were included. The delayed administration of immunosuppressive regimens was attempted in 11 liver recipients with multiple severe comorbidities.
The median duration of non-immunosuppression was 12 days (range 5-58). Due to the infectious complications, the serial ImmuKnow assay showed a significantly low ATP level of 64±35 ng/mL in the early period after transplantation. With the development of comorbidities, the ImmuKnow value significantly increased. However, the acute allograft rejection developed when a continuous distinct elevation of both ATP and glutamyltranspeptidase levels was detected. The average ATP level measured just before the development of acute rejection was 271±115 ng/mL.
The delayed introduction of immunosuppressive regimens is safe and effective in management of critically ill patients after liver transplantation. The serial ImmuKnow assay could provide a reliable depiction of the dynamics of functional immunity throughout the clinical course of a given patient.
在肝移植后发生感染性疾病或多器官功能障碍的患者中,免疫抑制治疗的调控仍然具有挑战性。我们通过 ImmuKnow 检测评估了在免疫监测下肝移植患者延迟引入免疫抑制治疗的结局。
2009 年 3 月至 2014 年 2 月,我院共纳入 225 例连续肝移植受者。对 11 例合并多种严重合并症的肝移植患者尝试延迟应用免疫抑制方案。
非免疫抑制治疗的中位持续时间为 12 天(范围为 5-58 天)。由于感染性并发症,移植后早期连续 ImmuKnow 检测显示 ATP 水平显著降低(64±35ng/ml)。随着合并症的发展,ImmuKnow 值显著增加。然而,当同时检测到 ATP 和谷氨酰转肽酶水平持续明显升高时,会发生急性移植物排斥反应。在发生急性排斥反应之前测量的平均 ATP 水平为 271±115ng/ml。
在肝移植后危重症患者的管理中,延迟引入免疫抑制方案是安全有效的。连续 ImmuKnow 检测可提供患者特定临床病程中功能性免疫动态的可靠描述。