Mice Engrafted with Human Fetal Thymic Tissue and Hematopoietic Stem Cells Develop Pathology Resembling Chronic Graft-Versus-Host Disease

    Jennifer L. Lockridge, Ying Zhou, Yusof A. Becker, Shidong Ma, Shannon C. Kenney, Peiman Hematti, Christian M. Capitini, William J. Burlingham, Annette Gendron‐Fitzpatrick, Jenny E. Gumperz
    TLDR Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.
    Researchers engrafted immunodeficient mice with human fetal thymic tissue and hematopoietic stem cells (HSCs), resulting in pathology resembling chronic graft-versus-host disease (cGVHD) observed in humans. The mice exhibited symptoms such as skin thickening, alopecia, lung inflammation, liver fibrosis, and eye irritation, typically developing more than 100 days post-transplantation. The study highlighted the critical role of the human thymic organoid in promoting T cell engraftment and cGVHD development, with regulatory T cells (FoxP3+ T cells) helping to limit disease severity. This humanized mouse model provided a valuable system for studying cGVHD and evaluating potential treatments.
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