Loss G E, Mason A L, Blazek J, Dick D, Lipscomb J, Guo L, Perrillo R P, Eason J D
Department of Surgery, Ochsner Multi-Organ Transplant Center, Ochsner Clinic and Foundation Hospital, New Orleans, LA 70121, USA.
Clin Transplant. 2001;15 Suppl 6:55-8. doi: 10.1034/j.1399-0012.2001.00010.x.
Here we describe a strategy for using livers from hepatitis B core antibody (anti-HBc) positive donors in anti-HBc negative recipients and report our preliminary results. Adult anti-HBc negative recipients were immunized against hepatitis B virus (HBV) prior to transplantation. Liver biopsies from anti-HBc positive, HBs Ag negative donors were performed at the time of procurement to rule out acute hepatitis or chronic liver disease. Donor serum and liver samples were collected for HBV DNA analysis by PCR. Recipients were given HBIG (10000 units, i.v.) during the anhepatic phase of transplantation. Patients were treated with lamivudine (150 mg) beginning on postoperative day (POD) 1. If HBV DNA was not detected in either donor liver or serum by PCR, recipient antiviral therapy was stopped. If donor liver and serum were positive for HBV DNA by PCR, the recipient was maintained on combination lamivudine and HBIG therapy. If HBV DNA was detected in donor liver but not in donor serum, the patient was managed on lamivudine therapy alone. Between February 1999 and June 2000, six anti-HBc negative recipients received liver transplants from anti-HBc positive donors. PCR analysis of serum from the six donors was negative for HBV DNA in each, while donor liver PCR analysis was positive in five of six for HBV DNA. Accordingly, all patients were given HBIG in the anhepatic phase of transplantation and five of six were maintained on daily lamivudine therapy. Follow-up periods have ranged from 2 to 18 months. There has been no emergence of de novo hepatitis B. Serial serum HBs Ag and HBV DNA assays have all proven negative. Moreover, while on lamivudine therapy, 2 patients now have undetectable HBV DNA in hepatic allograft biopsies by PCR analysis. Our strategy for using livers from anti-HBc donors has yielded promising initial results. De novo hepatitis B has not occurred and our data suggest residual hepatitis B virus may be eradicated in recipients maintained on lamivudine therapy.
在此,我们描述了一种在抗乙肝核心抗体(抗-HBc)阴性受者中使用抗-HBc阳性供者肝脏的策略,并报告我们的初步结果。成年抗-HBc阴性受者在移植前接受了乙肝病毒(HBV)免疫。在获取肝脏时,对来自抗-HBc阳性、乙肝表面抗原(HBs Ag)阴性供者进行肝脏活检,以排除急性肝炎或慢性肝病。收集供者血清和肝脏样本,通过聚合酶链反应(PCR)进行HBV DNA分析。受者在移植无肝期接受乙肝免疫球蛋白(HBIG,10000单位,静脉注射)。患者从术后第1天开始接受拉米夫定(150毫克)治疗。如果通过PCR在供者肝脏或血清中均未检测到HBV DNA,则停止受者的抗病毒治疗。如果供者肝脏和血清通过PCR检测HBV DNA呈阳性,则受者继续接受拉米夫定和HBIG联合治疗。如果在供者肝脏中检测到HBV DNA,但在供者血清中未检测到,则患者仅接受拉米夫定治疗。1999年2月至2000年6月期间,6名抗-HBc阴性受者接受了来自抗-HBc阳性供者的肝脏移植。对6名供者的血清进行PCR分析,结果显示每名供者的HBV DNA均为阴性,而6名供者中有5名的肝脏PCR分析显示HBV DNA呈阳性。因此,所有患者在移植无肝期均接受了HBIG治疗,6名患者中有5名继续每日接受拉米夫定治疗。随访期为2至18个月。未出现新发乙型肝炎。系列血清HBs Ag和HBV DNA检测均为阴性。此外,在接受拉米夫定治疗期间,通过PCR分析,2名患者的肝移植活检中现在检测不到HBV DNA。我们使用抗-HBc供者肝脏的策略已取得了有希望的初步结果。未发生新发乙型肝炎,我们的数据表明,接受拉米夫定治疗的受者体内残留的乙肝病毒可能被根除。