Cancer therapies that use immune cells to trigger the body to attack tumours could be improved by a molecule that boosts their function.
Studies with mice have found the improved therapies produced a powerful anti-cancer immune response, which led to tumours shrinking.
Initial experiments show the molecule has similar effects on human cells and could boost the success of cancer therapies for people.
Natural defence
The molecule – called LL-37 – is produced naturally by the body in response to infections and helps to kill harmful bacteria and viruses.
Scientists at the University of Edinburgh found it also influences immune cells and boosts their function.
In particular, the molecule boosts the function of specific cells that are responsible for initiating targeted immune responses – called dendritic cells.
Cell therapies
Dendritic cells have been used as cancer therapies because they can trigger other immune cells to recognise and attack tumours.
This approach typically involves taking a sample of the patients’ own cells and growing them in the lab under special conditions before infusing them back into the patient.
Clinical challenges
The process is expensive and has been hampered by difficulties with preparing sufficient numbers of dendritic cells that have the right characteristics for use as therapies.
Researchers at the University’s Centre for Inflammation Research found that adding LL-37 to dendritic cells while they are growing in the lab boosts yields of cells suitable for clinical use.
Mouse study
Treating mice with cells grown in this way helped to shrink tumours and, in some cases, led to complete clearance of the cancer.
Early tests suggest LL-37 has similar effects on human cells but further studies are needed, the researchers say.
The study, published in the journal Oncoimmunology, was funded by the Medical Research Council and the Royal Society.
We hope that our discovery will create new opportunities by overcoming some of the current road-blocks to effective use of dendritic cell-based cancer therapies.
