Share

Scientists make breakthrough in reversing treatment resistance in blood cancer patients

Researchers from the University of Southampton have identified why some people may become resistant to monoclonal antibodies, a common type of immunotherapy used in lymphoma treatment.

Encouragingly, in early studies they have demonstrated that adding an immune response stimulating drug called a ‘STING agonist’ could overcome drug-resistance in this type of blood cancer.

Results from the study, which was funded by the charities Bloodwise and Cancer Research UK, were published in the journal Cancer Research.

Lymphoma cells. Credit: University of Southampton

The monoclonal antibody rituximab has improved survival rates for many types of lymphoma, but not all patients respond and many will relapse. Researchers in Southampton have been studying how rituximab works and how to overcome resistance. They showed that rituximab works by stimulating specific white blood cells called macrophages, to engulf and ‘eat’ the lymphoma cells.

However, some lymphomas are able to suppress the macrophages by manipulating proteins called Fc-gamma receptors found on their surface to prevent engulfment. The findings help to explain why rituximab can be ineffective in some lymphoma patients.

The researchers then used a series of experimental immune stimulating drugs in combination with monoclonal antibodies to see if they could overcome resistance. In contrast to other immune system stimulators tested, one particular class of reagents called STING agonists were consistently able to stimulate macrophages, reverse the resistance and eliminate lymphoma cells in both mice and human cells in the laboratory when used in combination with monoclonal antibodies.

Dr Stephen Beers, who led the research with Professor Mark Cragg, said: “We’ve shown that STING agonists can help to ‘rev up’ immune cells and reverse attempts by the tumour cells to suppress them. There are promising early signs that this approach could be used to improve treatment for people with lymphoma. The next stage will be to modify STING agonists in the laboratory to make them as effective as possible at stimulating the immune system in lymphoma patients.”

Dr Alasdair Rankin, Director of Research at the blood cancer research charity Bloodwise, said: “Rituximab has helped to transform survival rates for many types of lymphoma and new ‘next generation’ monoclonal antibodies are improving treatment further, but not all patients will respond. While there is still a while to go before it reaches the clinic, the identification of drug combinations that can overcome treatment resistance could benefit a great many patients.”

Professor Peter Johnson, Cancer Research UK’s chief clinician, said: “Antibody treatments to harness the immune system have been one of the great success stories of modern cancer therapy, but we also know that cancers find many ways to escape from the immune system. This exciting research suggests that using drugs to re-programme the cells around a cancer may make antibody treatments much more effective in the future, and we should be able to start testing this in the clinic very soon.”