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Low risk of hepatitis B virus recurrence after withdrawal of long-term hepatitis B immunoglobulin in patients receiving maintenance nucleos(t)ide analogue therapy

机译:接受维持核苷酸(t)类似物治疗的患者停用长期乙型肝炎免疫球蛋白后乙型肝炎病毒复发风险低

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摘要

Hepatitis B virus (HBV) recurrence rates of 0-16% had been reported in patients maintained on nucleoside analogues (NA) after hepatitis B immunoglobulin (HBIG) discontinuation after orthotopic liver transplantation (OLT). However, follow-up in most studies was short. We aimed to determine the long-term risk of HBV recurrence using this strategy. All HBV patients who received ≥7 doses of intravenous HBIG after OLT, with no HBV recurrence while receiving HBIG, and who eventually discontinued HBIG and were maintained on NA, were included. HBV recurrence was defined as HBsAg-positive or HBV DNA ≥5 log copies/mL on 2 consecutive occasions. Twenty-one patients met the inclusion criteria. Immediate post-OLT prophylaxis was combination HBIG and NA in 15 patients, whereas 6 patients received HBIG monotherapy for 62-109 months before NA was added. HBIG was discontinued a median of 26 (range, 0.2-121) months after OLT. Median follow-up post-HBIG discontinuation was 40 (range, 5-51) months. Only 1 patient, who had 12 months of HBIG and was noncompliant to NA therapy, had HBV recurrence, 34 months after HBIG discontinuation. One patient had HBV DNA of 3.3 log copies/mL 47 and 48 months after HBIG discontinuation but remained HBsAg-negative. Lamivudine-resistant mutations were detected in both patients. Probability of HBV recurrence was 0% and 9% at 2 and 4 years after HBIG discontinuation. Three patients had 1-2 episodes of transiently detectable HBV DNA. All were HBV DNA and HBsAg negative on repeated tests over a period of 2-36 months. Maintenance therapy with NA after discontinuation of long-term HBIG therapy is associated with a low risk of HBV recurrence after OLT in compliant HBV patients. Liver Transpl 13:374–381, 2007. © 2007 AASLD.
机译:据报道,在原位肝移植(OLT)后停用乙肝免疫球蛋白(HBIG)后,维持核苷类似物(NA)的患者中,乙肝病毒(HBV)的复发率为0-16%。但是,大多数研究的随访时间很短。我们旨在使用该策略确定HBV复发的长期风险。纳入所有在OLT后接受≥7剂静脉HBIG且在接受HBIG时无HBV复发,最终终止HBIG并维持NA的HBV患者。 HBV复发定义为连续2次HBsAg阳性或HBV DNA≥5 log拷贝/ mL。 21名患者符合纳入标准。 OLT后立即进行预防的是15例患者接受HBIG和NA的联合治疗,而6例患者在加入NA之前接受了HBIG单药治疗62-109个月。 OLT停用HBIG的中位数为26(0.2-121)个月。 HBIG停用后的中位随访时间为40(5-51)个月。 HBIG停用后34个月,只有1名患者接受了12个月的HBIG且不符合NA治疗,但HBV复发。 HBIG停用后47和48个月,一名患者的HBV DNA为3.3 log拷贝/ mL,但HBsAg阴性。两名患者均检测到拉米夫定耐药突变。 HBIG停用后2年和4年,HBV复发的可能性分别为0%和9%。 3例患者有1-2次可瞬时检测到的HBV DNA。经过2-36个月的重复测试,所有患者的HBV DNA和HBsAg均为阴性。长期HBIG治疗中断后,NA维持治疗与依从性HBV患者接受OLT后HBV复发的低风险有关。 Liver Transpl 13:374–381,2007。©2007 AASLD。

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