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Creating “super soldiers” of specific white blood cells to boost an anti-tumor response has been shown in a series of elegant experiments by Princess Margaret researchers.

Research led by Ph.D. candidate Helen Loo Yau, Post-doctoral fellow Dr. Emma Bell and Senior Scientist Dr. Daniel D. De Carvalho describes a DNA modifying epigenetic therapy that can transform immune killer T-cells into “super soldiers” by boosting their ability to kill cancer cells.

Their findings could potentially enhance immunotherapy, a new paradigm in cancer treatment currently effective for a minority of cancer patients. Some patients respond well to immunotherapy, with their tumors drastically shrinking in size, diclofenac sod dr t but others respond only partially or not at all. Clinicians and scientists around the world are working to understand why immunotherapy only helps some patients.

The research is published in Molecular Cell, Feb 19, 2021.

“Our goal for the future is to use this strategy combined with other immunotherapies to enhance anti-tumor immunity,” says Dr. De Carvalho, Associate Professor, Department of Medical Biophysics, University of Toronto. “We imagine a future clinical trial where we collect T-cells from the patient for treatment with epigenetic therapy in the lab. This could expand the army of cancer killing cells effectively creating an ‘army of super soldiers’. These cells can then be re-infused into the patient, to potentially enhance their built-in immune response to the tumor.”

Dr. De Carvalho’s lab first observed an increase in T-cell infiltration in mouse tumors treated with epigenetic therapy. When they removed the T-cells, the therapy stopped working, suggesting that the T-cells were contributing to the treatment success.

Intrigued by this finding, the researchers set out to apply this epigenetic DNA modifying therapy directly to T-cells in the laboratory. They isolated T-cells from healthy human donors, as well as from patients with melanoma, breast, ovarian and colorectal cancer. Their results proved that the epigenetic therapy enhanced the T-cells cancer killing ability.

Epigenetics works through addition or removal of chemical ‘tags’ to DNA. Much like detachable post-it notes, these tags help to specify which genes can be turned on or off. Simply, you can change the function of a cell using drugs that change these epigenetic tags.

In essence, the researchers found that an available chemotherapy drug removed specific epigenetic tags that were keeping genes off in a subset of key genes in T-cells. Removing these tags turned these genes back on, and acted to “turbocharge” the T-cells to become more effective killing machines.

The researchers discovered two specific genes that were activated by the epigenetic therapy and which were responsible for the T-cells to become better at killing the cancer cells.

High-dimensional, single-cell mass cytometry analyses—a next generation technology, which profiles single cells and drug response—revealed an increase in the numbers of granzyme and perforin proteins, which T-cells use to carry out their killing function. When unleashed, like a lethal swat team, perforins are able to punch holes in a cell’s membrane to allow granzymes to enter into an infected or cancerous cell to finish the job of killing it.

“The T-cells became sort of ‘super soldiers’, with highly activated molecules—with bigger and better weapons—to destroy the cancer cells,” explains Dr. De Carvalho, adding the paper describes in detail the molecular mechanism of how the process occurs.

A key novelty in the paper is using epigenetic therapy to influence the behavior of genes in the T-cell. Most research on epigenetic therapies focuses on their effect on cancer cells. However, this paper looks at how our immune cells respond, giving insight into how we can boost the anti-tumor activity of our immune systems.

The emerging field of epigenetic therapy seeks to influence genetic activity without actually modifying the sequence of DNA—making this an exciting therapeutic avenue of cancer research.

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