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肝移植后乙型肝炎/丁型肝炎再感染的模式与机制

Patterns and mechanisms of hepatitis B/hepatitis D reinfection after liver transplantation.

作者信息

Zignego A L, Samuel D, Gentilini P, Bismuth H

机构信息

Istituto di Clinica Medica II, University of Florence, Italy.

出版信息

Arch Virol Suppl. 1993;8:281-9. doi: 10.1007/978-3-7091-9312-9_29.

Abstract

Viral recurrence is the limiting factor in orthotopic liver transplantation (OLT) for hepatitis B virus (HBV) related liver disease. In fact, high rates of HBV infection of the transplanted liver are reported, followed by the recurrence of liver disease in a high percentage of cases. The importance of reinfection stimulates the study of its modalities and mechanisms in order to better identify preventive measures and better select patients for OLT. In HBV and HDV positive patients, the outcome of liver transplantation appears significantly better than in patients that are solely HBV positive, in spite of a high rate of HDV reinfection. Long-term analysis (5 years) of HBV and HDV infection, using the PCR technique, in 15 patients transplanted for an HBV/HDV positive liver disease and treated with anti-HBs immunoglobulin (HBIG), revealed that all patients experienced an HDV reinfection, but only about 7 were still harboring the virus after four years of follow-up. HDV reinfection was either associated to HBV reinfection or isolated whereas no cases of HBV isolated reinfection was observed. Isolated HDV reinfection was frequent and transient in all but one case that was superinfected by HBV. Infected peripheral blood mononuclear cells seem to be implicated in HBV superinfection of HDV infected liver. Liver damage was observed only in cases of HBV/HDV co-infection, suggesting that, in vivo, HBV is necessary to produce liver damage although it is not essential for HDV absorption to target cells, HDV penetration of these cells or HDV genomic replication. In addition, in isolated HDV infection, transient HDV viraemia and its low levels suggest that, perhaps in these patients HDV uses a very limited presence of HBV or alternative ways which are not efficient enough for envelope production. These data suggest that, particularly in HDV positive patients, antiHBs Ig administration, which has previously been proven to significantly reduce HBV reinfection in HBsAg-positive patients, may be useful in changing the natural history of repetition of the original viral infection and liver disease after OLT.

摘要

病毒复发是乙型肝炎病毒(HBV)相关肝病原位肝移植(OLT)的限制因素。事实上,据报道移植肝的HBV感染率很高,随后相当高比例的病例会出现肝病复发。再感染的重要性促使人们对其方式和机制进行研究,以便更好地确定预防措施并更好地选择OLT患者。在HBV和HDV阳性患者中,尽管HDV再感染率很高,但肝移植的结果似乎明显优于单纯HBV阳性患者。对15例因HBV/HDV阳性肝病接受移植并用抗-HBs免疫球蛋白(HBIG)治疗的患者进行的长期(5年)HBV和HDV感染分析(采用PCR技术)显示,所有患者均经历了HDV再感染,但随访四年后只有约7例仍携带该病毒。HDV再感染要么与HBV再感染相关,要么为孤立性,而未观察到孤立性HBV再感染病例。除1例被HBV重叠感染的病例外,孤立性HDV再感染在所有病例中都很常见且短暂。受感染的外周血单核细胞似乎与HDV感染肝的HBV重叠感染有关。仅在HBV/HDV合并感染的病例中观察到肝损伤,这表明在体内,HBV虽然对于HDV靶向细胞的吸收、这些细胞的HDV穿透或HDV基因组复制不是必需的,但对于产生肝损伤是必需的。此外,在孤立性HDV感染中,短暂的HDV病毒血症及其低水平表明,也许在这些患者中,HDV利用了非常有限的HBV存在或效率不足以产生包膜的替代途径。这些数据表明,特别是在HDV阳性患者中,之前已被证明能显著降低HBsAg阳性患者HBV再感染的抗-HBs Ig给药,可能有助于改变OLT后原病毒感染和肝病复发的自然病程。

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