Researchers at the UC San Francisco (UCSF) have engineered T cells that only produce a strong anti-cancer cytokine when they come into contact with tumour cells. The immunotherapy successfully treated mice with melanoma and pancreatic cancer without causing any significant side effects, and it presents a promising new approach to combating these and other difficult-to-treat tumours.
The immune system normally produces the potent inflammatory chemical IL-2, which is delivered by the cells. It has powerful anti-cancer efficacy, which oncologists have known for years, but its usage has been constrained by the adverse reaction it causes when administered systemically.
In the study, published in the journal Science, the researchers were able to keep the cytokine contained within cancer by programming the tumour-infiltrating T cells to make their own IL-2 when they recognized a cancer cell.
"We've taken advantage of the ability of these cells to be local delivery agents and to crank out their T-cell amplifiers only when they recognize they're in the right place," said Wendell Lim, Ph.D., the Byers Distinguished Professor in cellular and molecular biology, director of the UCSF Cell Design Institute and senior author on the study. "I think this is a model for how we can use cell therapies to deliver many types of potent but toxic therapeutic agents in a much more targeted manner.”
Since the 1980s, oncologists have known that high doses of IL-2 enable T cells to overcome these barriers, and the cytokine has been used as a cancer therapy in challenging cancer cases. But simply infusing patients systemically with IL-2 can cause high fever, leaky blood vessels, and organ failure.
Lim and lead author Greg Allen, MD, Ph.D., adjunct assistant professor of medicine and a fellow at the Cell Design Institute, aimed to tame IL-2's effects by engineering cells that enhance the cancer-killing immune response only where it's needed: in the tumour. They chose to go after notoriously difficult-to-treat tumours, like those of the pancreas, ovary and lung, that form nearly iron-clad barriers against T cells.
To engineer cells T cells that could sense when they were in the tumour, the researchers used a synthetic Notch (or synNotch) receptor, a flexible type of molecular sensor, which Lim's lab developed several years earlier. These receptors span the cell membrane, with ends that protrude both inside and outside the cell. The outside portion recognizes and binds to tumour cells, triggering the inside portion to set the production of IL-2 in motion. The team tested the synNotch cells on a number of deadly tumours, including melanoma and pancreatic cancer, and found that the cells worked exactly as planned.
"We were able to design these therapeutic cells to slip past the tumour's defensive barriers. Once in the tumour, they could establish a foothold and begin effectively killing cancerous cells," said Allen. "We got on top of these tumours and in some cases cured them.”