Immune orchestrators stuck in cancers become “exhausted”
In a closely related study also published in Nature Communications, the research team led by Professor David Withers and Professor Menna Clatworthy also found that some dendritic cells (DCs), immune cell that play a key role in orchestrating anti-tumour immune response, get stuck within cancers.
The normal function of DCs is to capture material from cancer cells and deliver this to lymph nodes where they stimulate anti-tumour immune responses.
The team discovered that rather than trafficking to lymph nodes, some DCs stay in the tumour, where they become “exhausted”, with reduced ability to stimulate anti-tumour immune responses, and upregulation of cues that could even reduce anti-tumour immune cell function.
Identifying why these cells become trapped and how to overcome this impairment to normal DC behaviour has the potential to boost anti-tumour responses.
Menna Clatworthy, NIHR Research Professor and Professor of Translational Immunology at the University of Cambridge and co lead-author of the two studies said:
“We found that exhausted dendritic cells stuck in the tumour were located next to a type of tumour killer immune cell, CD8 T cells, potentially preventing them from doing their job. Remarkably, these dysfunctional tumour DCs could be revived using a cancer immunotherapy that’s used in the clinic.
"Our work helps develop our understanding of how cancers can disrupt the immune system, and crucially, how we can rescue this to improve anti-cancer immune responses.”