Dehghani Seyed Mohsen, Taghavi Seyed Ali Reza, Geramizadeh Bita, Nikeghbalian Saman, Derakhshan Nima, Malekpour Abdorrasoul, Malek-Hosseini Seyed Ali
Shiraz Transplant Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, IR Iran ; Gastroenterohepatology Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, IR Iran.
Hepat Mon. 2013 Jan;13(1):e6609. doi: 10.5812/hepatmon.6609. Epub 2013 Jan 1.
Despite the advances in the treatment of chronic hepatitis B virus (HBV) infection, liver transplantation (LT) remains the only hope for many patients with end-stage liver diseases resulting from HBV.
The aim of this study was to investigate the rate of HBV recurrence in cases that had undergone LT due to the HBV related liver cirrhosis.
Forty-nine patients who underwent LT due to HBV related cirrhosis since 2001 to 2009 in Shiraz Organ Transplantation Center were enrolled in the present study. They were asked to complete the planned questionnaire and also to sign the informed consent in order to take part in this study. Post-transplant prophylaxis protocol against HBV recurrence was based on a hundred milligrams of lamivudine daily plus intramuscular injections of hepatitis B immune globulin (HBIG) with appropriate dosage to keep anti-HBs antibody titer above 300 IU/L and 100 IU/L in the first six months and afterwards, respectively. Blood samples were obtained and checked for HBsAg, HBeAg, and the titers of Anti -HBsAb as well as Anti- HBeAb with ELISA. A quantitative HBV DNA assay was also done on all samples (GENE-RAD® Real-time PCR).
There were 91.8% males and 8.2% females enrolled in the study. The duration of post-transplant prophylaxis ranged from 3 months to 8 years (mean 18.9 ± 19.3 months). HBsAg and HBeAg were positive in 24.5% and 2% of cases, respectively. Real-time PCR for HBV DNA were zero copies/mL in 91.8% of patients, none of which represented a positive value for HBV recurrence (Positive > 10,000 copies/mL). The mean Anti-HBs Ab titer was 231.7 ± 135.9 IU/L; it was above 100 IU/L in 71.4% of patients. Thirty-seven (75.5%) of the patients were taking tacrolimus plus mycophenolate mofetil, 6 (12.2%) were on cyclosporine plus mycophenolate mofetil, and 6 (12.2%) were taking sirolimus plus mycophenolate mofetil. HBsAg was detectable in seven patients taking tacrolimus plus mycophenolate mofetil (18.9%), in four patients taking cyclosporine plus mycophenolate mofetil (66.7%), and in one patient among the six who were taking sirolimus plus mycophenolate mofetil (16.7%). There was no significant statistical correlation between the presence of a positive value for HBsAg and the immunosuppression regimen or Anti HBsAb titer (P ˃ 0.05). Presence of a positive value for HBsAg was not predictive of a positive HBV DNA or its level in blood (P ˃ 0.05).
Post-transplant HBV prophylaxis with lamivudine and intramuscular HBIG with appropriate dosage to keep anti-HBs antibody titer above 300 IU/L in the first six months and above 100 IU/L afterwards is effective for prevention of HBV recurrence after LT.
尽管慢性乙型肝炎病毒(HBV)感染的治疗取得了进展,但肝移植(LT)仍然是许多因HBV导致终末期肝病患者的唯一希望。
本研究旨在调查因HBV相关肝硬化接受LT的患者中HBV复发率。
纳入2001年至2009年在设拉子器官移植中心因HBV相关肝硬化接受LT的49例患者。要求他们填写计划好的问卷并签署知情同意书以参与本研究。针对HBV复发的移植后预防方案为每日口服100毫克拉米夫定加肌肉注射乙肝免疫球蛋白(HBIG),剂量适当,以使抗-HBs抗体滴度在前六个月及之后分别保持在300 IU/L和100 IU/L以上。采集血样,采用酶联免疫吸附测定法检测HBsAg、HBeAg、抗-HBsAb以及抗-HBeAb滴度。所有样本均进行HBV DNA定量检测(GENE-RAD®实时荧光定量PCR)。
本研究纳入的患者中男性占91.8%,女性占8.2%。移植后预防时间为3个月至8年(平均18.9±19.3个月)。HBsAg和HBeAg阳性率分别为24.5%和2%。91.8%的患者HBV DNA实时荧光定量PCR检测结果为零拷贝/毫升,均未出现HBV复发阳性值(阳性>10,000拷贝/毫升)。抗-HBsAb平均滴度为231.7±135.9 IU/L;71.4%的患者抗-HBsAb滴度高于100 IU/L。37例(75.5%)患者服用他克莫司加霉酚酸酯,6例(12.2%)服用环孢素加霉酚酸酯,6例(12.2%)服用西罗莫司加霉酚酸酯。服用他克莫司加霉酚酸酯的7例患者(18.9%)可检测到HBsAg,服用环孢素加霉酚酸酯的4例患者(66.7%)可检测到HBsAg,服用西罗莫司加霉酚酸酯的6例患者中有1例(16.7%)可检测到HBsAg。HBsAg阳性值的出现与免疫抑制方案或抗-HBsAb滴度之间无显著统计学相关性(P>0.05)。HBsAg阳性值不能预测血液中HBV DNA阳性或其水平(P>0.05)。
移植后采用拉米夫定和肌肉注射HBIG进行HBV预防,剂量适当,使抗-HBs抗体滴度在前六个月保持在300 IU/L以上,之后保持在100 IU/L以上,对预防LT后HBV复发有效。