Reagents for Targeted Ablation of Residual Contaminating Pluripotent Stem Cells

DESCRIPTION (provided by applicant): Human pluripotent stem (hPS) cells have great potential as a renewable source of cells for drug discovery, disease modeling and for transplantation to replace cells lost to degenerative diseases or injury. A critical barrier to the successful application of hPS cell research is the lack of methods for producing pure populations of hPS cell derivatives. Contaminating cells are both an issue for drug discovery where pure populations are needed for assay reproducibility and for transplantation where they present a safety issue because of their potential for tumor formation or differentiation to inappropriate cell types. Specifically, we propose here to address the problem of residual contaminating undifferentiated hPS cellsthat have the potential to form teratomas. We propose to develop hPS cell targeted toxins (hPS-CTTs) that kill residual hPS cells with minimal damage or alteration of the differentiated cell population. To achieve selective cell targeted toxicity, w willcombine an internalizing hPS selective targeting agent with the plant toxin, saporin, which is only toxic upon cellular internalization. This approach is much simpler than previously proposed genetic modification and physical separation methods that require cell manipulations that could alter or stress the desired cell population. It is also much more flexible than the previously proposed cytotoxic antibody because any internalizing antibody or peptide can be adapted for targeted cell killing. Moreover, the hPS-CTT is designed to be removed with the dead cells thus reducing its potential impact on the surviving cells. To demonstrate feasibility in phase I, we wil screen antibodies and peptides for selective hPS cell targeting. The cell targeting agents (CTAs) will be indirectly conjugated to a toxin, and tested for their ability to remove undifferentiated hS cells in a model cell system containing admixtures of differentiated hPS cells spiked with undifferentiated hPS cells. We will measure hPS cell contentbefore and after treatment by flow cytometry, the PluriTest, and quantitative RT-PCR. The ability to the optimal hPS-CTT to remove hPS cells will be tested using an in vivo teratoma assay. The persistence of the hPS-CTT in the treated population will be measured by western blot analysis and a functional assay to detect residual toxicity. A 2 component system that combines various targeting agents with secondary toxin conjugates will be used in phase I to show feasibility. In phase II, we will develop cell targeting agents directly conjugated to the toxin and further optimize protocols for hPS cell removal. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: We propose here to develop reagents that will facilitate safe human stem cell derived therapies by removing residual contaminating cells from therapeutic cell formulations. Replacement cells derived from human pluripotent stem cells have the extraordinary potential to treat virtually any condition where cells are lost to injury or disease (i.e. diabetes, heart disease, Parkinson's, and Alzheimer's). Unlike traditional drugs, cell based therapies carry an added risk of rogue cells that may persist in the patient for weeks, months or even years. For this reason cell identity and purity are critical for safe replacement cell therapies. Our proposed product is designed to selectively kill rogue contaminating tumor forming cells while leaving the therapeutic cells unharmed, thus enabling the manufacturing of human cell populations for safer cell-based therapies.