Gene Delivery Device to Make Engineered Cell Therapies Much Cheaper


Engineered cell treatments, such as CAR-T cell cancer immunotherapies and hematopoietic stem cell gene therapies, are extremely expensive. In large part that is because it’s not easy to grow myriads of precisely engineered cells that are originally sourced from the patient being treated.

Now, researchers at University of California, Riverside and City of Hope National Medical Center have come up with a technology that will make producing engineered cells easier, significantly reducing costs in the process.

The technology, called deterministic mechanoporation (DMP), consists of a microfluidic device that allows large numbers of living cells to be injected with genetic materials. Unlike the biochemical approaches that are typically used, the new approach is mechanical.

Using fluid flow, cells are dragged toward microscopic needles within the device. The cells are pierced and immediately pulled away by simply reversing the direction of the fluid they’re in. The resulting pore that is formed is large enough for genetic material present in the fluid to penetrate while leaving the cell healthy enough to continue its duties.

“This simple, but elegant nanomechanical poration approach provides significant advantages relative to existing gene delivery techniques,” said Masaru Rao, the lead researcher, in a press release. “For example, since viral vectors make up a large fraction of the overall manufacturing cost of current cell therapies, their elimination through the use of DMP holds potential for considerable cost reduction. In fact, in our paper we show that DMP can engineer primary human T cells, the same kind of cells used in CAR-T therapies, with efficiencies that exceed a state-of-the-art electroporation tool by more than four-fold,” Rao said.

The technology is being commercialized as SoloPore through a UC Riverside spinoff called Basilard BioTech.

Study in journal Nano Letters: Massively-Parallelized, Deterministic Mechanoporation for Intracellular Delivery

Via: University of California, Riverside

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