Division of Transplantation, Department of Surgery, University of Miami School of Medicine, Miami, FL 33136, USA.
Transplantation. 2011 Nov 15;92(9):1051-7. doi: 10.1097/TP.0b013e31822eb1f9.
We investigated the outcomes of adult liver transplants, according to their donor-recipient cytomegalovirus (CMV) serology.
We included in the study all adult primary liver transplants, from January 1, 2002, to December 31, 2005. Follow-up was until December 31, 2007. According to the donor-recipient CMV serology, patients were divided into positive-negative (PN), positive-positive, negative-negative, and negative-positive groups, and all received CMV prophylaxis for 4 months posttransplantation. Hepatitis C patients received conventional immunosuppression, whereas all other patients received either conventional treatment or alemtuzumab (Campath-1H) induction.
We studied 438 adult liver transplants. Comparisons were made between high-risk group patients (PN) versus all others: 5-year patient survival was 74.31% vs. 78.8%, (P=NS) and graft survival 63.87% vs. 74.77%, (P=0.042). Five-year freedom from rejection was 42.84% vs. 51.95% (P=0.036). CMV infection (n=3) or disease (n=27) was observed in 30 patients (PN [n=23], positive-positive [n=6], and negative-positive [n=1]). Incidence of CMV infection was 9.8% overall and 34.84% and 2.5%, respectively, for the PN group versus all others (P=0.0000). Patients who received Campath-1H induction did not have an increased incidence of CMV infections compared with those who received conventional immunosuppression.
In our center, in adult liver transplantation, CMV donor-recipient PN serology is associated with rejection, graft survival, and CMV infection but is not correlated with patient survival, Epstein-Barr virus (EBV) occurrence, or viral hepatitis recurrence. The introduction of more potent induction immunosuppression did not accentuate these negative outcomes.
我们根据供体-受者巨细胞病毒(CMV)血清学研究了成人肝移植的结果。
我们将 2002 年 1 月 1 日至 2005 年 12 月 31 日期间所有成人原发性肝移植纳入研究。随访至 2007 年 12 月 31 日。根据供体-受者 CMV 血清学,患者被分为正-负(PN)、正-正、负-负和负-正组,所有患者在移植后 4 个月内接受 CMV 预防。丙型肝炎患者接受常规免疫抑制治疗,而所有其他患者接受常规治疗或阿仑单抗(Campath-1H)诱导。
我们研究了 438 例成人肝移植。高危组患者(PN)与其他患者进行了比较:5 年患者存活率为 74.31%比 78.8%(P=NS),移植物存活率为 63.87%比 74.77%(P=0.042)。5 年无排斥反应的发生率为 42.84%比 51.95%(P=0.036)。30 例患者(PN [n=23]、正-正 [n=6]和负-正 [n=1])观察到 CMV 感染(n=3)或疾病(n=27)。CMV 感染的总发生率为 9.8%,PN 组分别为 34.84%和 2.5%,而其他组为 9.8%(P=0.0000)。与接受常规免疫抑制治疗的患者相比,接受阿仑单抗诱导的患者 CMV 感染的发生率没有增加。
在我们中心,在成人肝移植中,CMV 供体-受者 PN 血清学与排斥反应、移植物存活率和 CMV 感染相关,但与患者存活率、爱泼斯坦-巴尔病毒(EBV)发生或病毒性肝炎复发无关。引入更有效的诱导免疫抑制并未加剧这些负面结果。