Steering immune system with liposomes

Liposomes – nano-sized spheres composed of fatty molecules – are very promising for vaccination. Bio-pharmaceutical scientist Naomi Benne discovered that you can steer the immune response in animal models by varying the charge of the liposomes. She obtained her PhD degree on 8 September for this research, in which she studied possible treatments of cancer and atherosclerosis.

Treating cancer and atherosclerosis

Cancer and atherosclerosis are the two leading causes of death in the western world, with atherosclerosis being the predominant underlying pathology of cardiovascular disease. Their extremely high mortality rate is not the only thing these diseases have in common. Both conditions also influence the immune system, in particular our so-called T cells – the watchdog of our immune system. The difference, however, is that our T cells in cancer are underactive, while these cells are overactive in atherosclerosis. ‘Therefore, we believe that both diseases could be treated with vaccines that either activate or reduce the immune response,’ says the brand-new doctor Naomi Benne, who was supervised by professors Wim Jiskoot and Johan Kuiper and assistant professor Bram Slütter.

Cross-section of a liposome

Nano-sized spheres

In her thesis, Benne studied liposomes. These nano-sized particles are spherical and consist of roughly the same molecules as our cell membrane: lipids – molecules with a water-attracting head and a water-repelling tail. These lipids form a double layer, which surrounds a water core. ‘Liposomes are easy to make in the lab and they are very versatile,’ says the researcher. ‘They can carry both water-soluble compounds – such as proteins and peptides – in their water core, and compounds that are insoluble in water in their double layer.’ Another great feature of liposomes is that our body tolerates them very well. ‘Altogether, that makes them perfect for vaccine delivery.’

Charge matters

But can liposomes be effective in combatting cancer and atherosclerosis? To find this out, Benne took known antigens (see text frame below) and inserted them into positively and negatively charged liposomes. Next, she used these antigen-containing liposomes in animal models and studied the difference in effect between the charges.

A positively charged liposome appeared to wake up the watchdogs of our immune system. ‘We observed an inflammatory response, meaning that the antigen inside the liposomes activates the immune system, which in turn starts to attack cells in the body that correspond with this antigen. This could be useful for cancer treatment, as tumour cells suppress our immune cells so that they do not attack the tumour. A positively charged liposome with the right antigen could reverse this.’

Pathogen versus antigen

Traditionally, a pathogen is the virus or bacteria that makes you sick, while an antigen is a specific and unique part of the outside of a pathogen. Such an antigen can be used to train the immune system which cells, bacteria or viruses are safe, and which should be attacked, thereby curing diseases. In a more broad sense, an antigen is any molecular structure that can bind to our antibodies or immune cells and elicit an immune response. That is why a part of a patient’s tumour can also be used as an antigen. Antigens need a vehicle to reach the right part in our bodies, and that is where liposomes come into play.

A sleepy watchdog

When Benne used the same antigen inside a negatively charged liposome, she noticed something completely different. Now, the antigen helped to put the watchdogs down to sleep. ‘With a negatively charged liposome, the immune cells see the antigen as safe. This could be useful for treating auto-immune diseases such as atherosclerosis, in which the body starts to see normal and safe cells or proteins as a danger, eventually attacking them. With negatively charged liposome-based vaccines, we could train the immune system which cells are safe, thereby reversing the auto-immune response.’

Conveniently, it is easy to change the charge of a liposome, Benne explains. ‘You just start with different types of lipids that eventually form the liposome. It is a really simple technique.’

Personalised treatment

The outcomes are promising, but Benne stresses that results from animals models cannot be directly translated to humans. Benne: ‘In contrast to our models, people react differently to the same antigen. So you should determine for each patient which antigen works best, and then use liposomes to insert this personalised medicine. For cancer, you could for instance take a sample of the tumour and use this as an antigen. Either way, I think my PhD research shows the potential of liposomes in the treatment of immune-related diseases.’

Header image – Colorized scanning electron micrograph of a T cell. © NIAID

Text – Bryce Benda

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