A subset of immune cells that are stimulated to kill cancerous cells has now been discovered, which could now revolutionize cancer treatment.

Published in Immunity, scientists examined the molecular and cellular mechanisms underpinning this activity as part of an experimental study of immunotherapy in mice, funded by Cancer Research UK.
Researchers found that IL-2, a 'growth factor' for T cells and the 'transcription factor' Blimp-1, are responsible for initiating potent killer activity in CD4+ T cells within cancerous tumors.
Co-lead author, Professor Sergio Quezada (UCL Cancer Institute), said: "We knew these immune cells had the ability to kill cancer cells with incredible potency proactively, but to maximize their potential, we needed to know how this mechanism was activated.
"Our discovery provides the evidence and rationale for utilizing Blimp-1 to maximize the anti-tumor activity of CD4+ T cells. "Work is now underway in our lab to develop new personalized cell therapies where the activity of Blimp-1 can be maxed up to drive potent tumor control."
T cells are a subset of lymphocytes (white blood cells), which play a key role in the body's immune response. In immunotherapy, T cells are modified and used to attack cancer. These cells move around our bodies, looking for infected cells, and killing them. However, T cells do not recognize most cancers, since cancers develop from our own tissues and appear normal to most T cells.
"Much remains unknown regarding how best to optimize these therapies, particularly to enable better activity in solid organ cancers. "Our findings broaden our understanding of the regulators of T cell differentiation, illuminating new elements that might be targeted to enhance therapeutic efficacy."
"This work in the lab adds to growing evidence for the potential of immunotherapy and will hopefully lead to the development of more effective treatments for people affected by cancer."
Source-Eurekalert
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