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Scientists have developed a dual-function therapeutic strategy that converts live tumor cells into therapeutic drugs
.
Shah's team used the gene-editing tool CRISPR-Cas9 to engineer living tumor cells and repurpose them to release tumor cell killers
.
In addition, engineered tumor cells are engineered to express factors that make them easily discoverable, labeled, and remembered by the immune system, preparing them for a long-term anti-tumor response by the immune system
.
Scientists are using a new method to turn cancer cells into effective anti-cancer drugs
.
In the latest work in Khalid Shah's lab at Brigham and Women's Hospital, researchers have developed a new cellular therapy approach that eliminates established tumors and induces long-term immunity, training the immune system so that it can prevent cancer from returning
.
The team tested their dual-acting anti-cancer vaccine in an advanced mouse model of the deadly brain cancer glioblastoma, and the results were promising
.
The findings were published in the journal Science Translational Medicine
.
"Our team has been pursuing a simple idea: turning cancer cells into cancer killers and vaccines," said corresponding author Khalid Shah, Ph.
D.
, director of the Center for Stem Cell and Translational Immunotherapy (CSTI), associate director of Brigham's Division of Neurosurgery Research, and faculty
member at Harvard Medical School and the Harvard Stem Cell Institute (HSCI).
Through genetic engineering, we are repurposing cancer cells to develop a treatment that kills tumor cells and stimulates the immune system to destroy the primary tumor and prevent cancer
.
”
Cancer vaccines are an active area of research in many labs, but the approach taken by Shah and his colleagues is unique
.
Instead of using inactivated tumor cells, the team repurposed live tumor cells
with unusual characteristics.
Just as carrier pigeons return to their habitat, live tumor cells travel long distances in the brain back to their tumor cell companions
.
Using this unique property, Shah's team used the gene-editing tool CRISPR-Cas9 to engineer living tumor cells and repurpose them to release tumor cell killers
.
In addition, engineered tumor cells are engineered to express factors that make them easily discoverable, labeled, and remembered by the immune system, preparing them for a long-term anti-tumor response by the immune system
.
The team tested their repurposed CRISPR-enhanced and reverse-engineered therapeutic tumor cells (ThTCs) in different mouse strains, including bone marrow, liver, and thymus cells from humans, mimicking the human immune microenvironment
.
Shah's team also built a two-layer safety switch in cancer cells that, when activated, eradicated ThTC
if needed.
This double-acting cell therapy is safe, applicable and effective in these models, providing a roadmap
for treatment.
While further testing and development is needed, Shah's team specifically chose this model and used human cells to pave the way
for translating their findings into patient settings.
"In all the work we do at our center, even highly technical, we never neglect patients
," Shah said.
Our goal is to take an innovative but translatable approach so that we can develop a therapeutic anti-cancer vaccine that will ultimately have a lasting impact
on medicine.
Shah and colleagues note that this treatment strategy is applicable to a wider range of solid tumors and that further research
into its application is warranted.
Shah owns an equity stake in AMASA Therapeutics, a company
that develops stem cell-based cancer therapies.
Funding: This work was supported by the National Institutes of Health (grant R01-NS121096).
“Bifunctional cancer cell-based vaccine concomitantly drives direct tumor killing and antitumor immunity” Science Translational Medicine