Department of Surgery, Campus Virchow-Klinikum and Campus Charité Mitte, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Viruses. 2021 May 13;13(5):904. doi: 10.3390/v13050904.
Patients after LT due to combined HBV/HDV infection are considered to be high-risk patients for recurrence of hepatitis B and D. To date, life-long prophylaxis with hepatitis B immunoglobulin (HBIG) and replication control with nucleos(t)ide analogs (NA) remains standard. We examined the course of 36 patients that underwent liver transplantation from 1989 to 2020 for combined HBV/HDV-associated end-stage liver disease in this retrospective study. Seventeen patients eventually discontinued HBIG therapy for various reasons. Their graft function, histopathological findings from routine liver biopsies and overall survival were compared with those that received an unaltered NA-based standard regimen combined with HBIG. The median follow-up was 204 and 227 months, respectively. The recurrence of HBV was 25% and did not differ between the groups of standard reinfection prophylaxis NA/HBIG (21.1%) and HBIG discontinuation (29.4%); ( = 0.56). No significant differences were found regarding the clinical course or histopathological aspects of liver tissue damage (inflammation, fibrosis, steatosis) between these two groups. Overall, and adjusted survival did not differ between the groups. Discontinuation of HBIG in stable patients after LT for combined HBV/HDV did not lead to impaired overall survival or higher recurrence rate of HBV/HDV infection in this long-term follow-up. Therefore, the recommendation of the duration of HBG administration must be questioned. The earliest time of discontinuation remains unclear.
患有乙型肝炎病毒/丁型肝炎病毒(HBV/HDV)合并感染的肝移植(LT)患者被认为是乙型肝炎和丁型肝炎复发的高危人群。迄今为止,终身使用乙型肝炎免疫球蛋白(HBIG)预防和核苷(酸)类似物(NA)复制控制仍然是标准治疗方法。在这项回顾性研究中,我们检查了 1989 年至 2020 年间因 HBV/HDV 相关终末期肝病而接受肝移植的 36 例患者的病程。17 例患者因各种原因最终停止了 HBIG 治疗。我们比较了他们的移植物功能、常规肝活检的组织病理学发现以及总体生存率,与接受未改变的基于 NA 的标准方案联合 HBIG 治疗的患者进行了比较。中位随访时间分别为 204 个月和 227 个月。HBV 的复发率为 25%,两组之间没有差异:标准再感染预防 NA/HBIG 组(21.1%)和 HBIG 停药组(29.4%)(=0.56)。这两组在临床病程或肝组织损伤的组织病理学方面(炎症、纤维化、脂肪变性)没有发现显著差异。总体而言,两组的调整生存率没有差异。在 LT 治疗 HBV/HDV 合并感染的稳定患者中停止 HBIG 治疗不会导致总体生存率降低或 HBV/HDV 感染的复发率升高,这在长期随访中得到了证实。因此,HBG 给药持续时间的建议必须受到质疑。HBIG 停药的最早时间仍不清楚。