SEK 8 M / 3 YEARS
A BETTER PICTURE OF THE IMMUNE RESPONSE TO COVID-19 In this project Gunilla Karlsson Hedestam will map our immune response to new variants of the coronavirus, SARS-CoV-2, to understand how immunity is built up in the population – thereby putting us in a better position to respond to new virus variants and plan for future vaccinations.
“The immune system responds with its whole a rsenal, but only a small proportion of all the antibodies that the body produces in response to an infection or vaccination can actually neutralise the virus. We are interested in qualitative differences between different neutralising antibodies, and also whether individuals differ in terms of the type of antibodies they make,” she says. To analyse how the antibodies bind the virus at a detailed level Gunilla Karlsson Hedestam’s group has developed methods of isolating individual antibodies – known as monoclonal antibodies – from memory B cells to investigate which types of antibodies can neutralise different virus variants. “Our results to date have shown that certain anti bodies only neutralise the original virus, while other antibodies also neutralise the so-called variants,” she says. The project now receiving support from the Erling-Persson Foundation is called ‘Future-proofing against COVID-19’ and has various parts. “First we need to understand what the different virus variants are like, by analysing their family tree,” she says. “With sufficient volumes of data it is possible to distinguish which types of mutations the virus allows or does not allow,” says Gunilla Karlsson Hedestam. Here advanced modelling is required – something that her colleague Ben Murrell is expert at, having published data on the Alpha, Beta and Gamma virus variants in the scientific journal Cell. This type of monitoring is important for being able to predict how the virus may impact.
When the corona pandemic was a fact in March 2020, Gunilla Karlsson Hedestam, professor of vaccine i mmunology at Karolinska Institutet, already had a good idea of how viruses and anti-viral immune responses generally behave. “I’ve been working with antibodies to viruses since the early 1990s – particularly antibodies that target the outer structures of viruses, known as spike proteins. I spent a long time researching how anti bodies bind HIV, a particularly tricky virus. You could say spike proteins have followed me throughout my career,” she says. Both coronavirus and HIV use their spike proteins to get into their respective host cells and they are important targets for antibodies that in the best case block the virus’s ability to infect new cells. “When Covid-19 arrived we had the tools to quickly begin making spike proteins in the laboratory and we were able to rapidly set up various tests to investigate the occurrence of both antibodies and memory B cells in samples from infected individuals,” says Gunilla Karlsson Hedestam. Memory B cells act as a long-term archive that stores information from previous infections and vaccinations. The memory cells do not produce antibodies themselves, but they can be activated to become antibody-producing cells very quickly if we are infected by a substance that the immune system has seen before. In collaboration with Ben Murrell, her research group is investigating how different antibodies bind and block (neutralise) viruses. Spike proteins are big, so there are hundreds of different ways an antibody can bind to them.
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