Direct comparison of iPSC-CPCs and endogenous CPCs

  • Research type

    Research Study

  • Full title

    Therapeutic potential of human induced pluripotent stem cell-derived cardiac progenitor cells: Direct comparison with endogenous cardiac progenitor cells from the same patients

  • IRAS ID

    280250

  • Contact name

    Fiona Lewis-McDougall

  • Contact email

    f.lewis@qmul.ac.uk

  • Sponsor organisation

    Queen Mary University of London

  • Duration of Study in the UK

    3 years, 0 months, 0 days

  • Research summary

    Myocardial infarction and subsequent heart failure are the cause of more deaths, morbidity, and financial burden than any other group of diseases. Endogenous c-kit+ cardiac progenitor cells (eCPCs) have been shown to significantly alleviate cardiac damage in both acute and chronic settings however eCPCs are also susceptible to aging-related deterioration and their isolation requires an invasive cardiac biopsy. We hypothesise that a novel, expandable CPC population can be generated through generation of induced pluripotent stem cells (iPSCs) from patient skin cells followed by early selection of c-kit+ iPSC-CPCs. This offers unique advantages both as a research tool and a therapeutic cell source. To achieve this, we will directly compare human c-kit+ eCPCs and iPSC-CPCs from the same donors, which will define the optimal cell type to improve clinical outcome.

  • REC name

    London - Surrey Borders Research Ethics Committee

  • REC reference

    20/LO/0869

  • Date of REC Opinion

    31 Jul 2020

  • REC opinion

    Further Information Favourable Opinion