Joya-Vazquez Pedro P, Dodson Forrest S, Dvorchik Igor, Gray Edward, Chesky Amy, Demetris Anthony J, Shakil Obaid, Fung John J, Vargas Hugo E
Thomas E. Starzl Transplant Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Transplantation. 2002 May 27;73(10):1598-602. doi: 10.1097/00007890-200205270-00013.
The present scarcity of organ donors requires consideration of grafts from sources not previously used. Several studies have addressed the use of grafts from donors who have antibodies to the hepatitis B core antigen (anti-HBc+). The aim of this study was to evaluate the impact of the use of anti-HBc+ grafts in patients transplanted for hepatitis B virus (HBV)-related cirrhosis.
Recipients of first hepatic transplants from donors with antibodies to HBV were identified retrospectively. All patients who had serology suggestive of active HBV and were negative for hepatitis C and D were included in the analysis. The Kaplan-Meier method was used to assess the actuarial recurrence-free survival on patients with graft survival longer than 1.5 months. The stepwise Cox regression model was used to identify independent predictors of HBV recurrence.
One thousand seven hundred seventeen first liver transplants were performed at the Thomas E. Starzl Transplantation Institute from September 1, 1990, to December 31, 1999. HBV was the cause of cirrhosis in 112 patients (6.5%). Thirty-three patients had coexistent viral infection (23 HCV and 10 HDV). Fourteen donors (17.2%) were positive for HBV markers, with nine anti-HBc+ and with five both anti-HBc+ and anti-HB surface-positive; of these, 13 anti-HBc+ organ recipients had long-term survival. Nine (69.2%) of these cases were reinfected versus 20 (35.7%) in the group that received grafts from HBV- donors (P<0.05, Fisher's exact test). The mean time to reinfection was shorter in the anti-HBc+ group (2.9 yr vs. 6.4 yr, P<0.005). There were no statistical differences in graft or patient survival between the two groups. HBV prophylaxis with combined lamivudine and hepatitis B immunoglobulin (HBIG) significantly reduced the reinfection rate (P<0.03). Hepatitis Be (Hbe) antigen-positive recipients trended to faster reinfection (not significant). Cox regression analysis revealed that both anti-HBc graft donor status (RR, 2.796; P=0.020) and combination of lamivudine/HBIG (RR, 0.249; P=0.021) are independently associated with reinfection.
The use of anti-HBc+ liver grafts does not affect graft or patient survival. However, patients who receive these organs are 2.5 times more likely to develop HBV recurrence. Lamivudine and HBIG combination decreases HBV recurrence 4-fold.
目前器官供体短缺,需要考虑使用以前未使用过的来源的移植物。多项研究探讨了使用来自乙型肝炎核心抗原抗体阳性(抗-HBc+)供体的移植物。本研究的目的是评估在因乙型肝炎病毒(HBV)相关肝硬化接受移植的患者中使用抗-HBc+移植物的影响。
回顾性确定接受来自HBV抗体阳性供体的首次肝移植受者。所有血清学提示有活动性HBV且丙型肝炎和丁型肝炎阴性的患者纳入分析。采用Kaplan-Meier法评估移植存活超过1.5个月患者的无复发生存率。采用逐步Cox回归模型确定HBV复发的独立预测因素。
1990年9月1日至1999年12月31日,托马斯·E·斯塔兹尔移植研究所共进行了1717例首次肝移植。HBV是112例患者(6.5%)肝硬化的病因。33例患者合并病毒感染(23例丙型肝炎病毒和10例丁型肝炎病毒)。14例供体(17.2%)HBV标志物阳性,9例抗-HBc+,5例抗-HBc+和抗-HBs表面抗原均阳性;其中,13例抗-HBc+器官受者长期存活。这些病例中有9例(69.2%)再次感染相比接受HBV阴性供体移植物组的20例(35.7%)(P<0.05,Fisher精确检验)。抗-HBc+组再次感染的平均时间较短(2.9年对6.4年,P<0.005)。两组间移植物或患者存活率无统计学差异。拉米夫定和乙型肝炎免疫球蛋白(HBIG)联合预防HBV显著降低了再次感染率(P<0.03)。Hbe抗原阳性受者再次感染倾向于更快(无统计学意义)。Cox回归分析显示,抗-HBc移植物供体状态(RR,2.796;P=0.020)和拉米夫定/HBIG联合使用(RR,0.249;P=0.021)均与再次感染独立相关。
使用抗-HBc+肝移植物不影响移植物或患者存活。然而,接受这些器官的患者发生HBV复发的可能性高2.5倍。拉米夫定和HBIG联合使用可使HBV复发降低4倍。