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    Two-year safety outcomes of iPS cell-derived mesenchymal stromal cells in acute steroid-resistant graft-versus-host disease

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    Authors
    Kelly, K.
    Bloor, Adrian J C
    Griffin, J. E.
    Radia, R.
    Yeung, D. T.
    Rasko, J. E. J.
    Affiliation
    Haematology & Transplant Unit, The Christie NHS Foundation Trust, Manchester, UK.
    Issue Date
    2024
    
    Metadata
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    Abstract
    The first completed clinical trial of induced pluripotent stem cell (iPS cell)-derived cells was conducted in 15 participants with steroid-resistant acute graft-versus-host disease. After intravenous infusion of mesenchymal stromal cells (CYP-001 derived from a clone of human iPS cells), we reported the safety, tolerability and efficacy within the primary evaluation period at day 100. We now report results at the 2-year follow-up: 9 of 15 (60%) participants survived, which compares favorably with previously reported outcomes in studies of steroid-resistant acute graft-versus-host disease. Causes of death were complications commonly observed in recipients of allogeneic hematopoietic stem cell transplantation, and not considered by the investigators to be related to CYP-001 treatment. There were no serious adverse events, tumors or other safety concerns related to CYP-001. In conclusion, systemic delivery of iPS cell-derived cells was safe and well tolerated over 2 years of follow-up, with sustained outcomes up to 2 years after the first infusion. ClinicalTrials.gov registration: NCT02923375 .
    Citation
    Kelly K, Bloor AJC, Griffin JE, Radia R, Yeung DT, Rasko JEJ. Two-year safety outcomes of iPS cell-derived mesenchymal stromal cells in acute steroid-resistant graft-versus-host disease. Nature medicine. 2024 Jun;30(6):1556-8. PubMed PMID: 38778211. Pubmed Central PMCID: PMC11186752 described in this manuscript. D.T.Y. reports honoraria and research funding from Novartis. J.E.J.R. holds shares in Rarecyte and Woke Pharmaceuticals; reports data safety and monitoring board membership for the Fanconi anemia trial; has received grant and research support from the National Health and Medical Research Council (Investigator Grant), Cancer Council New South Wales, the Cancer Institute of New South Wales, the Medical Research Future Fund, Therapeutic Innovation Australia and philanthropic foundations; reports supply of material (via a material transfer agreement) or consultancy or honoraria from Rarecyte, Novartis, bluebird bio, Spark Therapeutics, Cynata Therapeutics, Pfizer and CRISPR Therapeutics; he reports membership on an entity’s board of directors or advisory committees as co-founder of AAVec Bio and nonexecutive director of Kennerton Capital; and is employed by the Sydney Local Health District at Royal Prince Alfred Hospital as Head of the Department of Cell & Molecular Therapies. A.J.C.B., J.E.G. and R.R. declare no competing interests. Epub 2024/05/23. eng.
    Journal
    Nature Medicine
    URI
    http://hdl.handle.net/10541/627037
    DOI
    10.1038/s41591-024-02990-z
    PubMed ID
    38778211
    Additional Links
    https://dx.doi.org/10.1038/s41591-024-02990-z
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.1038/s41591-024-02990-z
    Scopus Count
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