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Review
. 2015 Jan 27;7(1):121-6.
doi: 10.4254/wjh.v7.i1.121.

HBV and HIV co-infection: Impact on liver pathobiology and therapeutic approaches

Affiliations
Review

HBV and HIV co-infection: Impact on liver pathobiology and therapeutic approaches

Mohammad Khalid Parvez. World J Hepatol. .

Abstract

The consequences of hepatitis B virus (HBV) and human immunodeficiency virus (HIV) co-infection on progression of severe liver diseases is a serious public health issue, worldwide. In the co-infection cases, about 90% of HIV-infected population is seropositive for HBV where approximately 5%-40% individuals are chronically infected. In HIV co-infected individuals, liver-related mortality is estimated over 17 times higher than those with HBV mono-infection. The spectrum of HIV-induced liver diseases includes hepatitis, steatohepatitis, endothelialitis, necrosis, granulomatosis, cirrhosis and carcinoma. Moreover, HIV co-infection significantly alters the natural history of hepatitis B, and therefore complicates the disease management. Though several studies have demonstrated impact of HIV proteins on hepatocyte biology, only a few data is available on interactions between HBV and HIV proteins. Thus, the clinical spectrum as well as the complexity of the co-infection offers challenging fronts to study the underlying molecular mechanisms, and to design effective therapeutic strategies.

Keywords: Chronic hepatitis B; Hepatitis B virus; Hepatitis B virus and human immunodeficiency virus co-infection; Hepatopathogenesis; Human immunodeficiency virus; Human immunodeficiency virus-hepatotropism.

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Figures

Figure 1
Figure 1
A cartoon depiction of hepatitis B virus and human immunodeficiency virus co-infection of liver. Intracellular locations of the two viruses in hepatocytes, liver sinusoidal endothelial cells, Kupffer cells, portal mononuclear inflammatory cells, stellate cells, dendritic cells and Kupffer cells are shown (upper panel). The structural and genomic organizations of HIV and HBV indicating the probable trans-regulation of HBV-DNA and HBsAg by HIVgp120 (lower panel). PMIC: Portal mononuclear inflammatory cell; HIV: Human immunodeficiency virus; HBV: Hepatitis B virus; DNA: Deoxyribonucleic acid; HBsAg: Hepatitis B surface antigen; HBcAg: Hepatitis B core antigen; RT: HIV reverse-transcriptase.

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