SCIENTISTS CREATE TUMOUR-KILLING CELLS WHICH CAN BE DIRECTLY INJECTED INTO PATIENTS
In a breakthrough, scientists have for the first time
created cancer-killing cells which can be directly injected into patients. Researchers in Japan have created cancer-specific killer
T-cell, the cells naturally occur in small numbers, but it is hoped injecting
huge quantities back into a patient could turbo-charge the immune system.
Researchers at the RIKEN Research Centre for Allergy and
Immunology revealed they have succeeded for the first time in creating
cancer-specific, immune system cells called killer T lymphocytes.
To create these, the team first had to reprogramme T
lymphocytes specialized in killing a certain type of cell called induced pluripotent
stem cell (iPS cells). These iPS cells then generated fully active,
cancer-specific T lymphocytes. These lymphocytes regenerated from iPS cells
could potentially serve as cancer therapy in the future, researchers believe.
Previous research has shown that killer T lymphocytes
produced in the lab using conventional methods are inefficient in killing
cancer cells mainly because they have a very short life-span, which limits
their use as treatment for cancer.
To overcome the problems, Japanese researchers, led by
Hiroshi Kawamoto reprogrammed mature human killer T lymphocytes into iPS cells
and investigated how these cells differentiate. The team induced killer T lymphocytes specific for a certain
type of skin cancer to reprogram into iPs cells by exposing the lymphocytes to
the “Yamanaka factors” – a group of compounds that induce cells to revert to a
non specialized, stage.
The iPS cells obtained were then grown in the lab and
induced to differentiate into killer T lymphocytes again. This new batch of T
lymphocytes was shown to be specific for the same type of skin cancer as the
original lymphocytes.
They maintained the genetic reorganization, enabling them to
express the cancer-specific receptor on their surface. The new T lymphocytes
were also shown to be active and to produce an anti-tumour compound.
“We have succeeded in the expansion of antigen-specific T
cells by making iPS cells and differentiating them back into functional T
cells.” Kawamoto said.
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