Yang Yang, Zhang Qi, Cai Chang-jie, Lu Ming-qiang, Li Xi, Jiang Nan, Jiang Hua, Xu Chi, Li Hua, Wang Gen-shu, Yi Shu-hong, Zhang Jian, Zhang Jun-feng, Yi Hui-min, Zhang Ying-cai, Chen Gui-hua
Liver Transplant Center, Third Affiliated Hospital of Sun Yat-sen University, Transplantation Research Institute of Sun Yat-sen University, Guangzhou 510630, China.
Chin Med J (Engl). 2007 Aug 20;120(16):1400-3.
The most frequently used therapy for post-transplantation recurrence of hepatitis B virus (HBV) infection is lamivudine, but this drug is associated with a high resistance rate due to YMDD mutant. In preliminary reports, adefovir dipivoxil (ADV) has been shown to have activity against lamivudine-resistant strains of HBV. However, clinical experience in treatment of HBV infection after liver transplantation (LT) is still not entirely clear. This study was aimed to evaluate the prophylactic efficacy of ADV plus hepatitis B immunoglobulin (HBIG) in patients with YMDD mutant before LT.
From March 2004 to March 2006, 16 patients with chronic hepatitis B had lamivudine-resistant YMDD mutants detected prior to liver transplantation and received treatment with ADV plus additional intramuscular HBIG after LT as prophylaxis against graft reinfection. Tests for liver function, serum HBsAg, anti-HBs (HBIG), HBeAg, anti-HBc, anti-HBe, HBV-DNA, and creatinine were assessed pre- or post-liver transplantation.
The median follow-up of these patients post-liver transplantation was 19.4 months. Fifteen patients survived and one patient died of recurrence of hepatocellular carcinoma (HCC). There was significant difference (10.98% vs. 2.26%, P < 0.05) in YMDD mutant rate between the patients with HBV-DNA over 10(6) copies/ml and those with HBV-DNA less than 10(6) copies/ml. Fifteen patients (93.8%) had undetectable HBV-DNA at 4 weeks and 1 (6.3%) at 6 months after LT. No hepatitis B recurrence was detected by persistent testing of HBsAg, HBeAg, and HBV-DNA and no increase of serum creatinine level associated with ADV was observed in any of the patients.
ADV combined with intramuscular HBIG can effectively prevent patients with pre-transplantation YMDD mutant from HBV recurrence after LT.
乙肝病毒(HBV)感染移植后复发最常用的治疗方法是拉米夫定,但由于YMDD突变,该药物耐药率较高。在初步报告中,阿德福韦酯(ADV)已显示出对拉米夫定耐药的HBV毒株有活性。然而,肝移植(LT)后治疗HBV感染的临床经验仍不完全清楚。本研究旨在评估ADV联合乙肝免疫球蛋白(HBIG)对LT前YMDD突变患者的预防效果。
2004年3月至2006年3月,16例慢性乙肝患者在肝移植前检测出拉米夫定耐药的YMDD突变,并在LT后接受ADV联合额外肌肉注射HBIG治疗,以预防移植物再感染。在肝移植前后评估肝功能、血清HBsAg、抗-HBs(HBIG)、HBeAg、抗-HBc、抗-HBe、HBV-DNA和肌酐检测。
这些患者肝移植后的中位随访时间为19.4个月。15例患者存活,1例患者死于肝细胞癌(HCC)复发。HBV-DNA超过10⁶拷贝/ml的患者与HBV-DNA低于10⁶拷贝/ml的患者之间的YMDD突变率存在显著差异(10.98%对2.26%,P<0.05)。15例患者(93.8%)在LT后4周时HBV-DNA检测不到,1例患者(6.3%)在6个月时检测不到。通过持续检测HBsAg、HBeAg和HBV-DNA未检测到乙肝复发,且在任何患者中均未观察到与ADV相关的血清肌酐水平升高。
ADV联合肌肉注射HBIG可有效预防移植前YMDD突变患者LT后HBV复发。