Zheng Shusen, Wu Jian, Wang Weilin, Huang Dongsheng, Liang Tingbo, Lu Anwei
Department of Hepatobiliary Surgery, The First Affiliated Hospital of Medical College of Zhejiang University, Hangzhou 310003, China.
Zhonghua Yi Xue Za Zhi. 2002 Apr 10;82(7):445-8.
To discuss the effect of lamivudine as prophylaxis against hepatitis B virus (HBV) reinfection following orthotopic liver transplantation (OLT).
40 patients with HBV-related diseases received lamivudine, 100 mg/day, as prophylaxis against HBV reinfection after OLT. Hepatitis B serum markers, HBsAg, HBeAg, HBcAb-IgM, and HBcAg were detected every 2 weeks by immunohistochemistry. Serum HBV-DNA was examined by PCR every 2 weeks. Liver biopsy was conducted to the donor livers during operation and to the transplanted livers postoperatively in regular interval. HBsAg and HBcAg in the liver specimens were examined by immunohistochemistry. YMDD mutation sequencing was done to those patients with conversion of positive HBV DNA postoperatively.
The positive rates were 100%, 25%, and 30% for the serum HBsAg, HBeAg, and HBV DNA of the patients respectively before OLT. All 40 donor liver specimens showed negative HBsAg and HBcAg. HBV reinfection rates were 12.2% and 23.5% 6 months and 12 months after OLT respectively. HBeAg had been positive in 4 out of the 6 cases with postoperative reinfection and had been positive in 8 out of the 34 cases without reinfection (P = 0.4505). HBV DNA had been positive in 5 out of the 6 cases with postoperative reinfection, and had been positive in 7 out of the 34 cases without reinfection (P = 0.0461). After OLT HBV DNA converted to positive in 4 cases, mutation of YMDD locus (YMDD-YIDD) had been found in 3 of which.
Lamivudine monotherapy is effective against HBV reinfection after OLT. Given the lamivudine monotherapy, HBV reinfection causes mutation in YMDD locus on the HBV DNA polymerase gene. OLT does not apply in patients with positive HBV DNA. For those patients to be operated upon, lamivudine should be used to convert HBV DNA to negative beforehand.
探讨拉米夫定预防原位肝移植(OLT)术后乙肝病毒(HBV)再感染的效果。
40例HBV相关疾病患者接受拉米夫定预防OLT术后HBV再感染,剂量为100mg/天。每2周通过免疫组化检测乙肝血清标志物、HBsAg、HBeAg、HBcAb-IgM和HBcAg。每2周通过PCR检测血清HBV-DNA。术中对供肝进行肝活检,术后定期对移植肝进行肝活检。通过免疫组化检测肝组织标本中的HBsAg和HBcAg。对术后HBV DNA转为阳性的患者进行YMDD突变测序。
OLT术前患者血清HBsAg、HBeAg和HBV DNA的阳性率分别为100%、25%和30%。40例供肝标本的HBsAg和HBcAg均为阴性。OLT术后6个月和12个月的HBV再感染率分别为12.2%和23.5%。术后再感染的6例患者中有4例HBeAg阳性,未再感染的34例患者中有8例HBeAg阳性(P = 0.4505)。术后再感染的6例患者中有5例HBV DNA阳性,未再感染的34例患者中有7例HBV DNA阳性(P = 0.0461)。OLT术后4例患者HBV DNA转为阳性,其中3例发现YMDD位点突变(YMDD-YIDD)。
拉米夫定单药治疗对OLT术后HBV再感染有效。采用拉米夫定单药治疗时,HBV再感染会导致HBV DNA聚合酶基因YMDD位点突变。HBV DNA阳性患者不适合进行OLT。对于拟行手术的患者,应先使用拉米夫定将HBV DNA转为阴性。