Dan Shelly, PhD, on Advantages of Multi-Targeted OmniCAR Platform

Video

The vice president of business development and alliances at Prescient Therapeutics discussed the mechanism of the OmniCAR technology.

“We can show that when you add targeting ligand, you can get CAR activity that looks like the sigmoidal dose response curve of a small molecule, but for CAR activity, so that's really remarkable. We've also been able to show that we can arm, unarm, and rearm the cells. We've been able to show in human glioblastoma cells, we can co-culture cells that express either HER2 or EGFR, we can come in with a fully armed EGFR omniCAR T-cell, and we can kill just the EGFR-expressing cells and not the HER2 ones. Then, 20 hours later, which we hypothesize would be enough time for receptor turnover and proliferation, we just add a HER2 targeting ligand. At that point, we stop killing the EGFR cells, and we start killing the HER2 cells.”

Presicent Therapeutics’universal immune receptor chimeric antigen receptor (CAR) platform called OmniCAR is a controllable, multi-antigen targeting platform using a single cell product. The strategy, developed at University of Pennsylvania, consists of a decoupled antigen receptor and T-cell signaling domain. OmniCAR also uses a SpyTag/SpyCatcher binding system developed at Oxford University.

Dan Shelly, vice president, business development and alliances, Prescient Therapeutics, presented preclinical data on the OmniCAR platform at the World Oncology Cell Therapy Congress (WOCTC) held April 25-26 in Boston, Massachusetts. CGTLive spoke with Shelly to learn more about its advantages in manufacturing, durability of response, safety, and regulatory processes. He also explained the various parts of the OmniCAR construct, including the SpyTag and SpyCatcher binding domain.

Click here to read more coverage of WOCTC 2023.

REFERENCE
Shelly D. Post-infusion controllable CAR therapies with a novel universal immune receptor. Presented at: WOCTC; April 25-26; Boston, Massachusetts.
Recent Videos
Barry J Byrne, MD, PhD, the chief medical advisor of MDA and a physician-scientist at the University of Florida
Barry J Byrne, MD, PhD, the chief medical advisor of MDA and a physician-scientist at the University of Florida
Sarah Larson, MD, the medical director of the Immune Effector Cell Therapy Program in the Division of Hematology/Oncology at David Geffen School of Medicine at University of California, Los Angeles (UCLA)
Manali Kamdar, MD, the associate professor of medicine–hematology and clinical director of lymphoma services at the University of Colorado
Manali Kamdar, MD, the associate professor of medicine–hematology and clinical director of lymphoma services at the University of Colorado
Ben Samelson-Jones, MD, PhD, assistant professor pediatric hematology, Perelman School of Medicine, University of Pennsylvania and Associate Director, Clinical In Vivo Gene Therapy, Children’s Hospital of Philadelphia
Manali Kamdar, MD, the associate professor of medicine–hematology and clinical director of lymphoma services at the University of Colorado
Steven W. Pipe, MD, a professor of pediatric hematology/oncology at CS Mott Children’s Hospital
Haydar Frangoul, MD, the medical director of pediatric hematology/oncology at Sarah Cannon Research Institute and Pediatric Transplant and Cellular Therapy Program at TriStar Centennial
Related Content
© 2025 MJH Life Sciences

All rights reserved.