Mas A
ICU for Digestive & Metabolic Diseases, Hospital Clínic, IDIBAPS, Barcelona, Catalonia, Spain.
Dig Liver Dis. 2009 May;41 Suppl 2:S191-4. doi: 10.1016/S1590-8658(09)60443-6.
In the past, reinfection of the graft by hepatitis B virus (HBV) after liver transplantation for HBV-related liver disease was often followed by severe liver damage and reduced survival. The long-term administration of hepatitis B immunoglobulin (HBIG) dramatically reduced this risk. However, this procedure was ineffective in most patients with active viral replication pre-transplant. The use of lamivudine in the pre-transplant setting partially solved this problem. The emergence of resistant mutants to lamivudine was also solved by the addition of adefovir. At present, combination therapy by oral antivirals pre-transplant and HBIG plus the same drugs post-transplant achieves nearly 100% of protection against graft reinfection. In a recent study, a new intravenous HBIG, Niuliva has shown high efficacy in achieving protective anti-HBs levels after liver transplantation for HBV-related liver diseases, as well as a good safety profile. Using combination therapies, the doses of HBIG can be reduced or even stopped after several weeks or months post-transplant, continuing with oral antivirals alone. The recently introduced antivirals achieve a very high antiviral potency and low risk of resistance. This may further increase the efficacy in preventing graft reinfection in the post-liver transplantation setting.
过去,乙型肝炎病毒(HBV)相关肝病患者肝移植后,移植肝被HBV再次感染常伴随严重肝损伤和生存率降低。长期使用乙型肝炎免疫球蛋白(HBIG)可显著降低这种风险。然而,该方法对大多数移植前有活跃病毒复制的患者无效。移植前使用拉米夫定部分解决了这一问题。加用阿德福韦也解决了拉米夫定耐药突变体的出现问题。目前,移植前口服抗病毒药物联合移植后HBIG及相同药物的联合治疗对移植肝再感染的预防率接近100%。在最近一项研究中,一种新型静脉用HBIG——牛丽佳,在HBV相关肝病肝移植后达到保护性抗-HBs水平方面显示出高效性,且安全性良好。采用联合治疗时,移植后数周或数月后可减少甚至停用HBIG剂量,仅继续使用口服抗病毒药物。最近引入的抗病毒药物具有非常高的抗病毒效力和低耐药风险。这可能会进一步提高肝移植后预防移植肝再感染的疗效。