Cells from the immune system called CD4+ regulatory T cells, or simply Treg, are linked to tumour prognosis: the more Treg cells present in a tumour, the worst the prognosis.

We know from previous research studies that Treg cells can infiltrate into the tumour microenvironment. There, they inhibit anti-tumour immunity, which is the self-defence mechanism that the body puts in place to fight cancer cells, stimulating tumour growth.

However, how tumour-infiltrating Treg cells are activated and regulated was, until this study, unknown. A better understanding of how Treg cells contribute to tumour growth is the first step in designing novel therapies for melanoma and many other cancers.

In a study published in eLife, researchers from the University of Tsukuba have shown a mechanism through which small particles derived from cells modulate tumour-infiltrating Treg cells.

Extracellular vesicles (EVs) are particles released from cells that are delimited by a lipid bilayer containing functional biomolecules (proteins, lipids, and nucleic acids) that can be transferred to other cells.

EVs released from tumour cells (called tumour-derived EVs or TEVs) can act as messengers and are emerging as critical players in tumour progression and metastasis.

“We found that mice deficient in the inhibitory immunoreceptor CD300a on their dendritic cells have increased numbers of Treg cells in tumours and greater tumour growth compared with wild-type mice after transplantation of B16 melanoma”, explains Professor Akira Shibuya, senior author of the study.

If the absence of the CD300a receptor leads to increased Treg cells, one can conclude that these are related, and the next step of the study was to understand how.

By studying cells derived from melanoma, the researchers found that tumour-derived extracellular vesicles are the link they were seeking.

They bind to this inhibitory immunoreceptor called CD300a on dendritic cells, stopping them from producing IFN-β, a molecule that activates Treg cells. Therefore, by binding to CD300a, extracellular vesicles suppress the activation of tumour-infiltrating Treg cells and tumour development.

The study also looked at human samples.

“To examine the role of CD300A in tumour development in humans, we analysed the data on the single-cell RNA sequence of human melanoma tissues, showing that higher expression of CD300A was associated with decreased tumour-infiltrating Treg cells and longer survival time in patients with melanoma”, says Professor Shibuya.

These findings are of particular interest for oncology researchers and clinicians because they may pave the way for boosting the expression of CD300A to avoid the accumulation of Treg cells and consequent tumour development.

For patients, their families, and the wider community, these findings point towards potential new therapeutic targets for melanoma and other types of cancer.

Source: University of Tsukuba