High-Throughput Gene-Editing via Microfluidic Cell Deformability to Enable Off-the-Shelf Allogeneic Cellular Immunotherapies
Oncologists are increasingly interested in harnessing the power of their patients' immune systems to aide in the ongoing battle against cancer. One example, adoptive cellular therapies, utilizes types of white blood cells known as T-cells that have been genetically engineered to recognize and recruit other cells of the immune system to attack malignant cells. These approaches have shown promise in pediatric patients with difficult to treat leukemias, but are limited to specialized academic centers in part by how efficiently (and quickly) they can be manufactured as well as by technical limitations in the strategies commonly used to deliver biomolecules for gene modification.
To address these challenges, this proposal focuses on developing and applying microfluidic technologies that enable delivery of gene-editing agents into cells rapidly via temporary pores that form at cellular membranes as cells are squeezed through narrow channels. This strategy is gentler and less toxic than competing approaches which require the use of external electric fields. To avoid clogging of the device we propose to line the microchannels with bio-inspired surface chemistries that prevent cells from becoming stuck via a "slip and slide" effect. The proposed platform will be used to demonstrate rapid and efficient gene-editing of T-cells at scales compatible with mass production to overcome obstacles in the clinical translation and deployment of cellular immunotherapies.
Project Update (May 2018):
Combining his engineering and pediatric oncology background, Dr. Steven Jonas created a potentially time-saving and cost-efficient way to deliver childhood cancer treatments using nanotechnology. Nanotechnology refers to working with materials that are on the scale of a nanometer, which is the thickness of a piece of human hair sliced down 100,000 times.
He and his interdisciplinary group of chemists, engineers, and physician-scientists are building nanorobotic, gene-delivery drones to deploy genes and gene-editing packages directly to cells quickly, safely and for a lower cost than current delivery methods.
For kids battling cancer, this “tiny” technology has the potential to significantly reduce the wait time for delivery of precision medicine, like CAR T-immunotherapy from a month to weeks.
“The opportunity to continue to explore ‘outside the box’ ideas like this and move toward defeating childhood cancer once and for all with emerging cellular therapies has added so much to my pediatric oncology fellowship training and informed the next stage of my academic career and research,” said Dr. Jonas.