| Literature DB >> 35362861 |
Kevin Verhoeff1, Braulio A Marfil-Garza1,2,3, Nerea Cuesta-Gomez4, Ila Jasra4, Nidheesh Dadheech4, A M James Shapiro5,6,7.
Abstract
Islet cell transplant (ITx) continues to improve, with recently published long-term outcomes suggesting nearly 80% graft survival, leading to improvements in glycemic control, reductions in insulin doses, and near-complete abrogation of severe hypoglycemia. Unfortunately, access to ITx remains limited by immunosuppression requirements and donor supply. Discovery of stem cell-derived functional islet-like clusters with the capacity to reverse diabetes offers a renewable, potentially immunosuppression-free solution for future widespread ITx. Evaluation and optimization of these therapies is ongoing, but may one day provide a realistic cure for type 1 diabetes. However, stem cell-based ITx has unique immunologic questions that remain unanswered. Here, we briefly synthesize current approaches for stem cell-derived ITx, review humanized mice models, and elaborate on the potential of humanized mice models for bridging the gap between current small rodent models and human clinical trials for allogeneic and autologous inducible pluripotent stem cell (iPSC)-based ITx while highlighting limitations and future directions.Entities:
Keywords: Diabetes; Humanized mouse model; Immunosuppression; Inducible pluripotent stem cells; Islet cell transplant; Transplant
Mesh:
Year: 2022 PMID: 35362861 DOI: 10.1007/5584_2022_711
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 3.650