‘Tumour-trained’ immune cells – which have the potential to kill cancer cells – have been seen moving from one tumour to another for the first time. The new findings, which were uncovered by scientists at Australia’s Garvan Institute of Medical Research, shed light on how immune therapies for cancer might work, and suggest new approaches to developing anti-cancer immune therapies.
The study, which was carried out in mice, is published in the Proceedings of the National Academy of Sciences USA (PNAS).
Metastatic cancer, in which cancer has spread to other sites beyond the primary tumour, is responsible for almost all cancer deaths, and treatment options remain very limited. New immune therapies that help the body’s own immune T cells to attack cancer cells within tumours are showing promise in metastatic cancer—yet little is understood about how these therapies function.
“We know that T cells and other immune cells accumulate inside tumours—but until now we’ve known very little about what happens next. How does the environment within the tumour change the cells? Do they leave the tumour? Which types of immune cells leave? Where do they go, and why?” says Dr Tatyana Chtanova, head of the Innate and Tumour Immunology lab in Garvan’s Immunology Division, who led the research.
To watch ‘tumour-trained’ immune cells travelling through the body, Dr Chtanova and her team used an innovative ‘photoconversion’ strategy—in which all the cells in a mouse are labelled with a green fluorescent compound, and only those within a tumour (including immune cells) are turned to red by shining a bright light on the tumour.
“Before, we could only guess at which immune cells were leaving tumours,” says Dr Chtanova, “so to see these red cells moving in a sea of green, as they exited a tumour and travelled through the body, was remarkable.
“We saw immune cells leaving the tumour and moving into lymph nodes – and, importantly, we could see immune cells moving out of one tumour and into another, distant tumour.”
The researchers were surprised to see that the mix of immune cells leaving tumours was sharply different to the mix of immune cells going in.
“We found, unexpectedly, that T cells were the main immune cells to exit tumours and move to lymph nodes and other tumours – even though they represent only a fraction of the immune cells that enter tumours,” Dr Chtanova notes, “and some classes of T cell, such as CD8+ effector T cells which promote tumour destruction, were more likely to exit the tumour.
“This tells us that there’s strong control over the tumour-exiting process.”
Importantly, the T cells that had been exposed to the tumour’s ‘microenvironment’ and then exited the tumour were more activated, and had a stronger cytotoxic (cell-killing) activity, than those that did not enter the tumour.
“What we suspect is happening is that, within the tumour, these T cells are acquiring knowledge about the cancer that helps them to seek and destroy tumour cells.
“It’s possible that these T cells ‘on patrol’—which leave one tumour and move to another—are using their new-found knowledge to attack cancerous cells in the second tumour.”
The research team are now working on ways to prompt activated T cells to exit tumours in greater numbers.
“Ultimately, we’re working to understand more deeply the relationships between immune and cancer cells, so that we can design approaches to empower the immune system to destroy cancer,” Dr Chtanova adds.
Paper: Tommaso Torcellan el al., “In vivo photolabeling of tumor-infiltrating cells reveals highly regulated egress of T-cell subsets from tumors,” PNAS (2017). www.pnas.org/cgi/doi/10.1073/pnas.1618446114