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Hepatitis B Virus Infection in Human Immunodeficiency Virus Infected Southern African Adults: Occult or Overt – That Is the Question

机译:在人类免疫缺陷病毒感染乙肝病毒感染的南部非洲位:隐匿性或显性 - 这是个问题

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摘要

Hepatitis B virus (HBV) and human immunodeficiency virus (HIV) share transmission routes and are endemic in sub-Saharan Africa. The objective of the present study was to use the Taormina definition of occult HBV infection, together with stringent amplification conditions, to determine the prevalence and characteristics of HBV infection in antiretroviral treatment (ART)-naïve HIV+ve adults in a rural cohort in South Africa. The presence of HBV serological markers was determined by enzyme linked immunoassay (ELISA) tests. HBV DNA-positivity was determined by polymerase chain reaction (PCR) of at least two of three different regions of the HBV genome. HBV viral loads were determined by real-time PCR. Liver fibrosis was determined using the aspartate aminotransferase-to-platelet ratio index. Of the 298 participants, 231 (77.5%) showed at least one HBV marker, with 53.7% HBV DNA−ve (resolved) and 23.8% HBV DNA+ve (current) [8.7% HBsAg+ve: 15.1% HBsAg−ve]. Only the total number of sexual partners distinguished HBV DNA+ve and HBV DNA−ve participants, implicating sexual transmission of HBV and/or HIV. It is plausible that sexual transmission of HBV and/or HIV may result in a new HBV infection, superinfection and re-activation as a consequence of immunesuppression. Three HBsAg−ve HBV DNA+ve participants had HBV viral loads <200 IU/ml and were therefore true occult HBV infections. The majority of HBsAg−ve HBV DNA+ve participants did not differ from HBsAg+ve HBV DNA+ve (overt) participants in terms of HBV viral loads, ALT levels or frequency of liver fibrosis. Close to a quarter of HIV+ve participants were HBV DNA+ve, of which the majority were HBsAg−ve and were only detected using nucleic acid testing. Detection of HBsAg−ve HBV DNA+ve subjects is advisable considering they were clinically indistinguishable from HBsAg+ve HBV DNA+ve individuals and should not be overlooked, especially if lamivudine is included in the ART.
机译:乙型肝炎病毒(HBV)和人类免疫缺陷病毒(HIV)共享传播途径,在撒哈拉以南非洲流行。本研究的目的是利用隐匿性HBV感染的Taormina定义,以及严格的扩增条件,来确定抗病毒治疗(ART)-未使用过HIV + ve 的HBV感染的发生率和特征南非一个农村队列中的成年人。 HBV血清学标志物的存在通过酶联免疫法(ELISA)测试确定。 HBV DNA阳性是通过HBV基因组三个不同区域中的至少两个区域的聚合酶链反应(PCR)确定的。 HBV病毒载量通过实时PCR确定。使用天冬氨酸转氨酶与血小板的比率指数测定肝纤维化。在298名参与者中,有231名(77.5%)表现出至少一种HBV标记,其中53.7%的HBV DNA -ve (已解决)和23.8%的HBV DNA + ve (当前)[8.7%HBsAg + ve :15.1%HBsAg -ve ]。仅性伴侣总数区分了HBV DNA + ve 和HBV DNA -ve 参与者,暗示了HBV和/或HIV的性传播。 HBV和/或HIV的性传播可能是免疫抑制的结果,可能导致新的HBV感染,过度感染和重新激活。 3名HBsAg -ve HBV DNA + ve 参与者的HBV病毒载量<200 IU / ml,因此是真正的隐匿性HBV感染。大部分HBsAg -ve HBV DNA + ve 参与者与HBsAg + ve HBV DNA + ve 没有区别(公开)参与者的HBV病毒载量,ALT水平或肝纤维化频率。接近四分之一的HIV + ve 参与者是HBV DNA + ve ,其中大多数是HBsAg -ve ,只能通过核酸检测酸测试。考虑到他们与HBsAg + ve HBV DNA + ve <在临床上没有区别,建议对HBsAg -ve HBV DNA + ve 对象进行检测/ sup>个体,因此不应忽视,特别是如果ART中包含拉米夫定的话。

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