Chronic hepatitis B: an immunotherapy molecule can counteract it

There are over 300 million people in the world affected by it chronic form of hepatitis Bamong the first risk factors for liver cirrhosis etliver mood. In patients affected by this chronic infection, the immune system is unable to eradicate the virus responsible for the disease, which continues to survive and reproduce inside the liver cells. A group of researchers from the Vita-Salute San Raffaele Hospital and University, thanks to close collaboration with the American start-up Asher Biotherapeutics, has experimented for the first time in the world, in preclinical modelsa molecule capable of reactivating the immune system against chronic hepatitis B.

The results, published today in the prestigious scientific journal Science Translational Medicine, lay the foundations for the clinical development of an immunotherapy for this serious pathology. The study was coordinated by the professor Matteo IannaconeDirector of the Division of Immunology, Transplants and Infectious Diseases of the IRCCS San Raffaele Hospital and returned to Italy, after a long research experience in the United States, thanks to the Career Development Award from the Armenise-Harvard Foundation.

The hepatitis B virus

The hepatitis B virus (HBV) is transmitted by contact with infected blood, sexually or from mother to child during childbirth. Unlike what happens when an adult contracts the virus, over 90% of children infected at birth develop the chronic form of hepatitis B. In patients affected by this chronic infection, the immune system is unable to eradicate the virus responsible for the disease, which continues to survive and reproduce within liver cells. Currently there is a preventive vaccine for the disease, but patients who are already affected cannot benefit from it. Scientific research is progressing considerably in the field of antivirals, making San Raffaele an international point of reference. The research of Matteo Iannacone's group, in close collaboration with the unit directed by Professor Luca Guidotti, deputy scientific director of the Institute, has in fact contributed in recent years to developing some of the antivirals now commonly used to treat the disease in its chronic form .

How to awaken the immune system

What does the ineffectiveness of the immune system depend on and how can its action be reawakened? The researchers had already answered this question with some data published in Nature in 2019. The researchers had demonstrated, through a molecular analysis carried out thanks to intravital microscopy techniques, that T lymphocytes, cells of the immune system responsible for attacking the HBV virus , are unable to eradicate the infection and are dysfunctional from the moment they are activated. The work of characterizing dysfunctional T lymphocytes had also allowed the San Raffaele researchers to identify more suitable and effective molecules for reawakening these cells. Among these there is theinterleukin-2, a messenger molecule of the immune system, which acts as a sort of immunotherapy, already successfully tested both in cultured cells, obtained from patient samples, and in animal models. Interleukin-2, unfortunately, if administered systemically, produces serious side effects: it increases the permeability of blood vessels, causing severe edema. This happens because the molecule is not only able to reach its target, the T lymphocytes, but also acts on Natural Killer cells – which induce toxicity, and also on regulatory cells which inhibit the immune response.

The new study

The results just published in the journal Science Translational Medicine add a piece to those published in 2019. Thanks to the collaboration with the company Asher Biotherapeutics which produces interleukin-2, the researchers managed to experiment with this molecule, developing an approach called ” cis-targeting”: interleukin-2, conjugated with a specific antibody, can only target T lymphocytes, activating them correctly against the disease. We have seen – on mouse models of disease – that, by administering this type of immunotherapy, T lymphocytes expand in number and increase their function, i.e. they release cytokines capable of inhibit viral replication and eliminate infected cells, effectively killing the viruscomments Professor Matteo Iannacone

The results have therefore demonstrated, in preclinical models of hepatitis B and in the blood of healthy people, the safety, low toxicity and therapeutic efficacy of this innovative approach. In addition to antiviral approaches, it is possible to finally think about an immunotherapy strategy. The next step is to test this approach on humans, in combination with antivirals, concludes the researcher

Corriere della Sera also on Whatsapp. sufficient click here to subscribe to the channel and always be updated.