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New immunotherapy 鈥榟ighly effective鈥 against hepatitis B virus

14 May 2021

Scientists at 果冻影院 have identified a new immunotherapy to combat the hepatitis B virus (HBV), the most common cause of liver cancer in the world.

Transmission electron microscopic image revealed the presence of HBV particles

Each year, globally, chronic听HBV causes an estimated 880,000 deaths from liver cirrhosis and hepatocellular carcinoma/liver cancer (HCC).

The pioneering study used immune cells isolated directly from patient liver and tumour tissue,听to show听that targeting acyl-CoA:cholesterol acyltransferase (ACAT), an enzyme that helps to manage cholesterol levels in cells*, was highly effective at boosting immune responses.

Published in听Nature Communications, the findings show that blocking the activity of ACAT with ACAT inhibitors boosts the specific immune cells that can fight both the virus and associated cancerous tumours, demonstrating its effectiveness as an immunotherapy. Inhibiting ACAT was also found to impede HBV鈥檚 own replication, thereby also acting as a direct antiviral. ACAT inhibitors such as听avasimibe, taken orally, have previously been shown to be well-tolerated as cholesterol-lowering drugs in humans.

Explaining the study, lead author Professor Mala Maini (果冻影院 Division of Infection & Immunity), said: 鈥淐hronic hepatitis B virus infection is a major global health problem and the most common cause of liver cancer in the world.

鈥淭he development of novel therapeutic options is crucial to improve patient care. Immune cells such as T cells are indispensable for fighting viruses and tumours but are often highly dysfunctional and fail to control these diseases. Current standard of care treatments are often incapable of eliminating the virus, do not prevent cancer development and do not rescue immune cells.

鈥淚n this study we aimed to identify a treatment target to directly inhibit the virus while also boosting the immune cells fighting it.鈥

Cholesterol is a lipid (fat) that we ingest every day in our diets and that can exert multiple functions within different cells of the body. HBV infects the liver, an organ highly enriched in cholesterol and well known for limiting local immune responses.

In this study, using human liver disease tissue samples听in vitro, Professor Maini鈥檚 lab at 果冻影院 showed that ACAT inhibitors boosted human antiviral T cells capable of eliminating the virus. This response is in contrast to currently available therapies. The immune-boosting effect was especially striking in T cells found in the HBV-infected liver and within liver cancer, overcoming the local restraints on immune cell function, allowing the T cells to target both the virus and cancerous cells.

The Maini group then collaborated with Professor Jane McKeating鈥檚 lab at the University of Oxford to show that ACAT inhibitors could also block the HBV life cycle in a way that other antivirals are unable to. These drugs therefore have a unique combination of antiviral and immunotherapeutic effects.

Commenting on the findings, first author Dr Nathalie Schmidt (果冻影院 Division of Infection & Immunity), said: 鈥淲e have found a highly effective novel target for the treatment of chronic hepatitis B virus infection and liver cancer.

鈥淢odulating cholesterol metabolism with ACAT inhibitors has the unique features of directly targeting the virus and tumours while at the same time boosting the T cells that fight them. This enables us to tackle the disease from multiple directions at the same time.鈥

Dr Schmidt added: 鈥淭he cholesterol-modifying drug is already known to be safe in humans and we hope that our study now informs the development of clinical trials combining cholesterol modulation with other immunotherapies. In summary, our findings offer exciting new possibilities for the treatment of patients with chronic viral infections and cancer.鈥

This research was carried out by researchers at 果冻影院, supported by the University of Oxford, the Royal Free London NHS Trust, and Leiden University Medical Centre, the Netherlands.

Grant funding came from the Wellcome Trust and Cancer Research UK.

*The enzyme is required for cholesterol esterification,听a mechanism which prevents excessive cellular levels of cholesterol, which can be toxic to cells.

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Image

  • This transmission electron microscopic (TEM) image revealed the presence of hepatitis B virus (HBV) particles. The round virions, which measure 42nm in diameter, are known as Dane particles. Credit: CDC/ Dr. Erskine Palmer on , CC BY 2.0

Media contact

Henry Killworth

Tel: +44 (0) 7881 833274

E: h.killworth@ucl.ac.uk