In blood cancers such as chronic lymphocytic leukaemia, B cells of the immune system multiply uncontrollably. One form of therapy involves labelling the CD20 protein on the surface of the B cells with customised antibodies. This triggers a chain of immunological reactions and ultimately leads to the destruction of the cancer cells.

Such immunotherapeutic antibodies have been used against tumour diseases for 30 years. ‘Although it is crucial for the success of the therapy, we still know very few details about how the antibodies bind to CD20 and how the subsequent reactions take place,’ says Professor Markus Sauer from the Biocentre of Julius-Maximilians-Universität (JMU) Würzburg in Bavaria, Germany.

Tracking Down the Effectiveness of the Antibodies

This is now likely to change: A team led by the JMU biophysicist has developed a new super-resolution microscopic method. It makes it possible for the first time to investigate the interactions of therapeutic antibodies with target molecules on tumour cells in 3D with molecular resolution.

‘We can now observe how effectively the antibodies work and thus contribute to the development of improved therapies,’ says Markus Sauer.

The new microscopic method is termed LLS-TDI-DNA-PAINT. In the scientific journal Science, first author Dr Arindam Ghosh and a team from Markus Sauer's chair describe how the newly developed technology works and what findings have already been obtained with it. Dr Thomas Nerreter and Professor Martin Kortüm from the Medical Clinic II at Würzburg University Hospital were also involved in the study.

B Cells Take on the Shape of a Hedgehog

The Würzburg researchers carried out their studies on fixed and living Raji B cells using the new microscopy method. This cell line originates from a patient's Burkitt's lymphoma and is often used in cancer research. The researchers brought the cells into contact with one of the four therapeutic antibodies RTX, OFA, OBZ and 2H7.

All four antibodies crosslink the CD20 molecules in the cell membrane, resulting in strong localised accumulations of the antibodies. This activates the so-called complement system and initiates the killing of the cells by the immune system. In contrast to the current classification of therapeutic antibodies, the results show that the concatenation of the CD20 molecules occurs independently of whether the antibodies belong to type I or II.

The experiments also show that all four antibodies crosslink CD20 molecules that are located at specific sites on the membrane - on micrometre-long protrusions of the membrane called ‘microvilli’. At the same time, the binding of the therapeutic antibodies polarises the B cell and the outstretched microvilli are stabilised. As a result, the B cells take on a kind of hedgehog shape because the membrane protrusions are only located on one side of the cell.

The Next Steps in Research

What happens next? ‘The previous classification of therapeutic antibodies into types I and II can no longer be maintained,’ says Dr Arindam Ghosh. Until now, research has assumed that therapeutic antibodies of type I have a different mechanism of action than those of type II. However, the Würzburg studies disprove this.

‘The hedgehog shape makes the B cells appear as if they want to form an immunological synapse with another cell,’ says the JMU researcher. It is conceivable that the treated B cells activate macrophages and natural killer cells of the immune system in this way. The research team now will clarify whether this assumption is correct in further studies.

Funding

This work was funded by the European Research Council, the German Federal Ministry of Education and Research and the German Research Foundation.