“Lab on a chip” technology can be used to create individualized treatments for cancer
November 6, 2018
“This technology is particularly exciting because it dismantles major challenges in cancer treatments,” Weian Zhao says. Steve Zylius / UCI
Irvine, Calif., Nov. 6, 2018 — A new immunotherapy screening prototype developed by University of California, Irvine researchers can quickly create individualized cancer treatments that will allow physicians to effectively target tumors without the side effects of standard cancer drugs.
UCI’s Weian Zhao and Nobel laureate David Baltimore with Caltech led the research team that developed a tracking and screening system that identifies T cell receptors with 100-percent specificity for individual tumors within just a few days. Research findings appear in Lab on a Chip. (Link to study: https://pubs.rsc.org/en/content/articlepdf/2018/lc/c8lc00818c?page=search)
In the human immune system, T cells have molecules on their surfaces that bind to antigens on the surface of foreign or cancer cells. To treat a tumor with T cell therapy, researchers must identify exactly which receptor molecules work against a specific tumor’s antigens. UCI researchers have sped up that identification process.
“This technology is particularly exciting because it dismantles major challenges in cancer treatments,” said Zhao, an associate professor of pharmaceutical sciences who is affiliated with the Chao Family Comprehensive Center and the Sue & Bill Gross Stem Cell Research Center. “This use of droplet microfluidics screening significantly reduces the cost of making new cancer immunotherapies that are associated with less systemic side effects than standard chemotherapy drugs, and vastly speeds up the timeframe for treatment.”
Zhao added that traditional cancer treatments have offered a one-size-fits-all disease response, such as chemotherapy drugs which can involve systemic and serious side effects.
T cell receptor (TCR)-engineered T cell therapy, a newer technology, harnesses the patient’s own immune system to attack tumors. On the surface of cancer cells are antigens, protruding molecules that are recognized by the body’s immune system T cells. This new therapy places engineered molecules on the patient’s T cells which will bind to their cancer cell antigens, allowing the T cell to destroy the cancer cell. TCR therapy can be individualized, so each patient can have T cells designed specifically for their tumor cells.
This antigen-TCR recognition system is very specific – there can be hundreds of millions of different types of TCR molecules. A big challenge for TCR-T cell therapy development remains in identifying particular TCR molecules out of a pool of millions of possibilities. Finding a match can take up to a year (time many cancer patients don’t have) and can cost half a million dollars or more per treatment.
By using miniscule oil-water droplets, Zhao’s team designed a device that allows for individual T cells to join with cancer cells in microscopic fluid containers. The TCRs that bind with the cancer cells’ antigens can be sorted and identified within days, considerably faster than the months or year that previous technologies required. The technology also significantly reduces the cost of making individualized TCRs and accelerates the pipeline of TCR-T cell therapy to clinic.
Through a partnership with Amberstone Biosciences, a UCI start-up, this entire platform and screening process will be available to pharmaceutical companies for drug development within just a few months. Not only can this technology help revolutionize TCR-T cell therapies for cancer, but it will also be a powerful tool for discovering other immunological agents, including antibodies and CAR-T cells, and for elucidating new immunology and cancer biology at a depth not possible before.
Aude I. Segaliny, Lingshun Kong, Ci Ren, and Xiaoming Chen of UCI contributed to this work, in addition to Guideng Li, Jessica K. Wang and Guikai Wu. This work was supported by UCI Applied Innovation, the Chao Family Comprehensive Cancer Center, the Sue & Bill Gross Stem Cell Research Center and the Department of Pharmaceutical Sciences. The work was funded by National Institutes of Health (grants 1DP2CA195763 and R21CA219225) and Amberstone Biosciences LLC: No. AB-208317.
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