A large international team of researchers has conducted genetic engineering on T cells as a way to combat pancreatic cancer. In their paper published in the journal Nature Biomedical Engineering, the group describes engineering certain kinds of T cells and how well the approach worked when tested under laboratory conditions.
Pancreatic cancer is one of the deadliest forms of cancer—five years after diagnosis, only 5 percent of patients are still alive. The reasons for the high death rate are a lack of symptoms until the cancer is in a late stage and because it spreads so easily and quickly. It has also proven to be more difficult to treat than most other types of cancers. In recent years, medical researchers have begun looking at the possibility of using immunotherapy to battle the disease in which they attempt to induce the immune system to attack tumors.
For immunotherapy to be effective, T cells must be able to reach tumors and then to kill them. Tumor cells in the pancreas are typically covered by stroma tissue that makes it difficult to use drugs to kill them—immune cells have no such problems. Also, prior research has shown that tumors in the pancreas emit a substance called CXCL16 that attracts non-T cell immune cells that are not capable of attacking the tumors—their presence interferes with immune cells that are capable of mounting an attack.
In this new effort, the researchers focused on a type of T cell that has shown an ability to destroy pancreatic tumors—but does not do so because it lacks the proper receptor that would make it be attracted to CXCL16. To overcome this problem, the researchers gave the T cells the missing receptor using genetic engineering.
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