A precise measure of protective immunity
New tool aims to make HCV vaccine search easier
Around 71 million people worldwide are infected with the hepatitis C virus (HCV). One reason why no vaccine against the virus has been found to date is that there are numerous virus variants, some of which differ by more than 30% from each other. Scientists from TWINCORE, the Hannover Medical School (MHH) and the Helmholtz Centre for Infection Research (HZI) in Braunschweig have now succeeded in developing a test system that precisely measures the protective effect of an immune response against the large spectrum of HCV pathogens. They recently published their results in the scientific journal Gut.
To develop such a benchmark, the researchers at TWINCORE first examined so-called neutralising antibodies from the blood of 104 HCV-positive patients. These endogenous defence molecules play a central role in the immune response. They are produced both during an infection with a pathogen and after a vaccination. They bind viruses and disable them. The researchers were initially interested in how well the antibodies can neutralise as many different HC viruses as possible.
„This is a central question for vaccine development. You don’t know beforehand which virus you will be dealing with,“ says Dr Dorothea Bankwitz, scientist at the Institute for Experimental Virology at TWINCORE and first author of the study. „A vaccine therefore has to build up immunity that protects against infection with very many different variants.“
Based on these findings, they used bioinformatics methods to divide the viruses into six different groups, known as clusters. „There is no obvious genetic connection between the viruses in the same neutralisation clusters as we know it from the virus strains. However, they behave very similarly in terms of their susceptibility to antibodies,“ says Prof. Alice McHardy, head of the „Bioinformatics of Infection Research“ group at the HZI.
In the further course of the study, the researchers show that painstakingly analysing the effect of antibodies against all test viruses is not necessary. „It is sufficient to use a test virus from each of the clusters as an example to measure how well the antibodies protect against different HCV variants,“ says Akash Bahai, bioinformatician in McHardy’s team. This is a major improvement and a very effective method for assessing the potency of vaccine candidates in the future.
However, this discovery also has another special relevance for vaccine development: „Until now, it was assumed that one had to vaccinate with genetically very different HCV variants in order to build up broad protection. Now we have learned that the variants react differently to antibodies, regardless of their genetic background,“ says Prof. Thomas Pietschmann, Director of the Institute for Experimental Virology at TWINCORE and head of the research project. „It is probably better to immunise against representatives of the virus clusters in order to build up a broadly protective immune response. The clusters we have found can now form a basis for this.“ The researchers therefore hope that the test system they have created will help in the further search for a vaccine against HCV.
A large part of this research project was not carried out in the laboratory, but on the computer. „That’s the norm these days,“ says Pietschmann. „Therefore, we are very happy that we are perfectly networked with bioinformaticians. The RESIST Cluster of Excellence, in which researchers from TWINCORE, the MHH and the HZI are involved, and the German Centre for Infection Research (DZIF) offer us the optimal conditions for this.“
Contact for scientific information:
Prof. Dr. Thomas Pietschmann, email@example.com
Tel: +49 (0)511 220027-130
Dorothea Bankwitz, Akash Bahai, Maurice Labuhn, Mandy Doepke, Corinne Ginkel, Tanvi Khera, Daniel Todt, Luisa J Ströh, Leona Dold, Florian Klein, Frank Klawonn, Thomas Krey, Patrick Behrendt, Markus Cornberg , Alice C McHardy, Thomas Pietschmann
Hepatitis C reference viruses highlight potent antibody responses and diverse viral functional interactions with neutralising antibodies