Investigational human monoclonal antibody shows potential for treating chronic hepatitis B and hepatitis D
USA: A recent preclinical study published in the Journal of Hepatology has shown the potential of an engineered investigational human monoclonal antibody for the treatment of chronic hepatitis B and hepatitis D.
Based on the results of the study involving the Heidelberg University Hospital, German Center for Infection Research (DZIF), US company Vir Biotechnology, and University Medical Center Hamburg-Eppendorf, clinical trials with the monoclonal antibody VIR-3434 are ongoing.
Affecting hundreds of millions of people, chronic hepatitis B (HBV) is a widespread global health problem for which there is as yet no cure. Chronic hepatitis B virus infection poses a severe threat to approximately 300 million people worldwide, leading to liver disease and cancer. Approximately four percent of affected persons are chronically coinfected with the hepatitis delta virus (HDV), which exacerbates the gravity of the disease. Current treatments provide only limited cure rates and necessitate indefinite times of therapy.
A team around DZIF scientists from Heidelberg and Hamburg-Eppendorf supported the preclinical development of VIR-3434, a monoclonal antibody (mAb) discovered by Vir Biotechnology, Inc., that specifically targets the hepatitis B surface antigen (HBsAg) located in the viral envelope. This preclinical study shows how the engineered investigational human monoclonal antibody effectively prevents viral dissemination and reduces the amounts of viral particles and antigen in a mouse model for HBV/HDV coinfection.
A targeted approach
The researchers isolated and screened several monoclonal antibodies from memory B cells of HBV-vaccinated individuals that specifically target a conformational epitope (an epitope formed through the three-dimensional folding of the protein bringing distant amino acids together) within the antigenic loop of the small hepatitis B surface antigen. Among a series of more than 30 generated antibodies, which were tested using the most advanced in vitro infection system available and established at Heidelberg University Hospital, one mAb named HBC34 demonstrated potent neutralisation activity against HBV and HDV. The latter is a satellite virus that hijacks HBV surface proteins to infect human hepatocytes. The activity has been shown to be pan-genotypic, providing evidence that HBC34 neutralises all known genotypes of HBV and HDV. Modifications in the structure of the HBC34 mAb for improved potency generated VIR-3434 as a promising mAb candidate for clinical development.
“Aside from the potent neutralisation activity of VIR-3434, we engineered the Fc-portion of the mAb-the tail end of the antibody molecule that is crucial in the immune response-to increase binding to certain immune cells,” explains the co-first and corresponding author of the paper, Dr Florian Lempp, director of virology at Vir. “VIR-3434 has the potential to rapidly eliminate both viral and subviral particles from circulation.”
The researchers then tested VIR-3434’s neutralisation capability in a human liver-chimeric mouse model developed at the University Medical Center Hamburg-Eppendorf (UKE) by the team around Prof. Maura Dandri, a DZIF-scientist on viral hepatitis at UKE and co-author of the paper. The livers of these mice are populated with primary human hepatocytes-the only cell type infected by HBV and HDV in humans. The in vivo studies were essential to demonstrate that the in vitro selected mAb, VIR-3434, was able to block viral dissemination in the liver of both HBV-infected and HBV/HDV-coinfected mice.
“We found that VIR-3434 not only neutralises HBV and HDV infection with high potency in vivo,” explains the co-first author of the study Dr Tassilo Volz, “but it also effectively reduces viraemia-the number of viruses in the bloodstream-and the levels of circulating viral antigens in chronically infected animals.”
"VIR-3434 may provide a potential new option for treating patients with chronic hepatitis B and D, and aid in the prevention of these diseases. The antibody's strong neutralisation properties and promising results in our preclinical infection model may offer hope for patients worldwide," adds Prof. Dandri.
Testing VIR-3434 in the clinic
Based on the findings, clinical studies to ascertain the safety and efficacy of VIR-3434 in human subjects are already underway. The researchers hope that VIR-3434, which is also being studied in combination with other investigational agents, may provide a much-needed therapy to combat chronic hepatitis B and D and the devastating consequences of chronic infection with these viruses.
“The successful isolation and characterisation of VIR-3434 could mark a significant turning point in hepatitis B and D treatment. If further validated through clinical trials, this mAb may offer an important therapeutic option for patients with chronic hepatitis B and D,” emphasises co-author and DZIF-scientist Prof. Stephan Urban of Heidelberg University Hospital.
The described research on VIR-3434, which incorporates Xencor Xtend™ technology (an innovative platform that allows the prolongation of the half-life of antibodies), is the result of a successful collaboration of scientists within the German Center for Infection Research (DZIF) and with the industry partner Vir. The project fits into the DZIF bridging topic “Antibody-based therapies”, which aims to connect experts across DZIF’s different research areas to advance the development, production and clinical testing of therapeutic monoclonal antibodies.
Reference:
Florian A. Lempp, Tassilo Volz, Elisabetta Cameroni, Fabio Benigni, Jiayi Zhou, Laura E. Rosen, Julia Noack, Fabrizia Zatta, Hannah Kaiser, Siro Bianchi, Gloria Lombardo, Stefano Jaconi, Lucia Vincenzetti, Hasan Imam, Leah B. Soriaga, Nadia Passini, David M. Belnap, Andreas Schulze, Marc Lütgehetmann, Amalio Telenti, Potent broadly neutralizing antibody VIR-3434 controls hepatitis B and D virus infection and reduces HBsAg in humanized mice, Published:July 15, 2023DOI:https://doi.org/10.1016/j.jhep.2023.07.003.
