UCSF Team Engineers 'Safety Switches' for Immune Therapies
Bacterial Proteins Could Serve as Cellular Brakes in Immune-Based Cancer Therapies
By Kristen Bole | UCSF.edu | July 24, 2012
A UCSF team has harnessed a natural protein in bacteria to create a "pause switch" in immune cells, potentially leading to more effective and safer immune therapies for diseases such as cancer and multiple sclerosis.
These "effector proteins" are produced by some bacteria to protect themselves from their host's immune system and work by infiltrating immune cells and shutting down the immune response long enough to allow the bacteria to replicate.
In new findings published online July 22 in the journal Nature, the team of cellular engineers showed that they could remove those effector proteins from bacteria and engineer them into yeast or human immune T cells to create a "pause switch" in the engineered cell.
Ultimately, they hope to program that pause switch into immune therapies to make them easier to control and thus less prone to side effects.
Immune therapies are a growing interest in several fields, particularly cancer and autoimmune diseases, such as multiple sclerosis and diabetes. The goal of these therapies is to either bolster the immune system to kill diseased cells, such as cancer cells, or calm down an overactive immune response, as occurs in autoimmune diseases. Immune therapies are showing increasing promise in the clinic, but those therapies can be difficult to control in the body and can end up killing healthy host cells as well as their targets, researchers said.
"There's a lot of excitement now about harnessing the immune system to combat cancer and autoimmune diseases," said senior author Wendell Lim, PhD, a Howard Hughes Medical Investigator and professor of Cellular and Molecular Pharmacology at UCSF. "It's been well established that we can retrain the immune system to attack disease cells, but you have to do it in a controlled way. It's like learning to ski — the first thing you have to learn is how to stop."
Normally, when researchers engineer T cells for therapeutic use, the only way to stop those cells from being overactive is to insert DNA encoding a "self-destruct" switch, which destroys the cells. This new approach tells the cells to pause, rather than die.
Lim, who oversees the UCSF Cell Propulsion Lab, focuses his cellular engineering research on creating a cellular tool kit – the brakes, gas and steering wheel — for scientists to insert into biological therapies to control them better, just as we hone chemistry-based drugs to make them more precise and less toxic.