Abstract

Hepatitis Delta virus (HDV) is a satellite of the Hepatitis B virus (HBV) and causes severe liver disease. The estimated prevalence of 15–20 million infected people worldwide may be underestimated as international diagnostic guidelines are not routinely followed. Possible reasons for this include the limited awareness among healthcare providers, the requirement for costly equipment and specialized training, and a lack of access to reliable tests in regions with poor medical infrastructure. In this study, we developed an HDV rapid test for the detection of antibodies against the hepatitis delta antigen (anti-HDV) in serum and plasma. The test is based on a novel recombinant large hepatitis delta antigen that can detect anti-HDV in a concentration-dependent manner with pan-genotypic activity across all known HDV genotypes. We evaluated the performance of this test on a cohort of 474 patient samples and found that it has a sensitivity of 94.6% (314/332) and a specificity of 100% (142/142) when compared to a diagnostic gold-standard ELISA. It also works robustly for a broad range of anti-HDV titers. We anticipate this novel HDV rapid test to be an important tool for epidemiological studies and clinical diagnostics, especially in regions that currently lack access to reliable HDV testing.

Highlights

  • We show the development of an Hepatitis Delta virus (HDV) rapid test

  • Our results indicate that the HDV rapid test can successfully identify positive samples with a broad range of anti-HDV levels but does not react to samples with low ELISA signals in the negative control range

  • We provide a comprehensive performance evaluation of the HDV rapid test compared to a diagnostic ELISA using a cohort of 474 pre-characterized samples

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Summary

Introduction

Hepatitis delta virus (HDV) infections present the most severe health burden among viral liver diseases. As a satellite virus of the Hepatitis B virus (HBV), transmission takes place via co-infection with HBV or super-infection of patients with chronic hepatitis B (CHB). Persisting infection leads to the establishment of chronic hepatitis D (CHD), which significantly increases the risk of cirrhosis, hepatocellular carcinoma, and acute liver failure, leading to a reduced life expectancy [1,2,3,4]. For viral entry into hepatocytes, HDV requires the integration of the Hepatitis B virus S-antigen (HBsAg) into its envelope [10,11,12]. Vaccination against HBV protects against HDV co-infection, but not against HDV super-infection of HBV carriers. Vaccination coverage gaps remain worldwide [17]

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