TherVacB – a new therapeutic vaccine
A team of researchers around Prof Ulrike Protzer from Helmholtz Munich and Technical University of Munich (TUM) are currently investigating a new therapeutic vaccine against HBV, called TherVacB. The consortium of leading virologists, immunologists and physicians specialized in treating viral hepatitis, will use the newly designed vaccine as an immunotherapy to cure HBV. TherVacB will be evaluated in a clinical trial, starting in 2023 and conducted in Europe and Africa.
However, there is a major challenge in vaccine development: vaccines need a cold chain for transportation and storage to ensure their efficacy. Maintaining the cold chains at a specific temperature range can be difficult especially for resource-constrained countries and may result in vaccine damage or wastage. This problem can be alleviated if vaccines are stable at higher temperatures.
Resistant to heat exposure
To facilitate the distribution of TherVacB worldwide without the necessity of a cold chain, first authors Dr Julia Sacherl and Dr Anna Kosinska as well as their colleagues developed thermostable components of the vaccine. The results were now published in the Journal of Hepatology Reports. The researchers could show that the heat-stable vaccine components are well tolerated and allow inducing immune responses and control the virus in preclinical mouse models even after long-term exposure to high surrounding temperatures.
The findings of the researchers are a crucial step in the development of TherVacB, that will be tested in a clinical trial in 2023. In addition, the discovery will facilitate vaccine application worldwide, not only reducing the costs of vaccination campaigns but also easing the application of the therapeutic vaccine. A great benefit for many hepatitis B patients worldwide.
Original publication
Sacherl; Kosinska: A thermostable therapeutic vaccine is able to break immune tolerance in a mouse model of chronic hepatitis B, JHEP Reports (2022), DOI: https://doi.org/10.1016/j.jhepr.2022.100603.
Funding information
The study was supported by the German Center for Infection Research via TTU 05.715 and 05.813, the German Research Foundation via TRR179, project TP18, and by the Federal Ministry of Education and Research (BMBF) via the program Research KMU Innovativ16 – StabVacHepB AZ 031B0094C. Julia Sacherl received a stipend from the “Stiftung der deutschen Wirtschaft“ (sdw, German industrial foundation), Jinpeng Su from the Chinese Scholarship Council, and Helene Kerth was supported by the TRR179 with an MD student scholarship.
