Targeted Cellular Micropharmacies: Cells Engineered for Localized Drug Delivery

Thomas J. Gardner(Kettering University), Christopher M. Bourne(Cornell University), Megan M. Dacek(Cornell University), Keifer G. Kurtz(Cornell University), Manish Malviya(Kettering University), Leila Peraro(Kettering University), Pedro C. Silberman(Cornell University), Kristen Vogt(Memorial Sloan Kettering Cancer Center), Mildred J. Unti(Cornell University), Renier J. Brentjens(Memorial Hospital), David A. Scheinberg(Cornell University)
Cancers
August 5, 2020
Cited by 29Open Access
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Abstract

The recent emergence of engineered cellular therapies, such as Chimeric antigen receptor (CAR) CAR T and T cell receptor (TCR) engineered T cells, has shown great promise in the treatment of various cancers. These agents aggregate and expand exponentially at the tumor site, resulting in potent immune activation and tumor clearance. Moreover, the ability to elaborate these cells with therapeutic agents, such as antibodies, enzymes, and immunostimulatory molecules, presents an unprecedented opportunity to specifically modulate the tumor microenvironment through cell-mediated drug delivery. This unique pharmacology, combined with significant advances in synthetic biology and cell engineering, has established a new paradigm for cells as vectors for drug delivery. Targeted cellular micropharmacies (TCMs) are a revolutionary new class of living drugs, which we envision will play an important role in cancer medicine and beyond. Here, we review important advances and considerations underway in developing this promising advancement in biological therapeutics.


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