| Literature DB >> 26680606 |
Pia Montanucci1, Alessia Alunno2, Giuseppe Basta3, Onelia Bistoni4, Teresa Pescara5, Sara Caterbi6, Ilaria Pennoni7, Vittorio Bini8, Roberto Gerli9, Riccardo Calafiore10.
Abstract
Human umbilical cord Wharton jelly-derived mesenchymal stem cells (hUCMS) might apply to treating chronic autoimmune disorders, as already shown for Sjögren's syndrome, including type 1 diabetes mellitus (T1D). Since naked hUCMS grafts encountered restraints, we enveloped hUCMS, within immunoisolatory microcapsules (CpS-hUCMS), made of our endotoxin-free, clinical grade alginate. We then examined the vitro effects of interferon (IFN)-γ-pretreated CpS-hUCMS on Th17 and Treg of T1D patients (n=15) and healthy controls (n=10). Peripheral blood mononuclear cells (PBMCs) were co-cultured with PBMC/CpS-hUCMS: lymphocyte proliferation was assessed by carboxyfluorescein succinimidyl esther (CFSE) dilution assay, and phenotypic analysis of regulatory and effector Tc was also performed. Cytokine expression was performed by bead array and qPCR on IFN-γ-pretreated hUCMS before PBMCs co-culture. CpS-hUCMS restored a correct Treg/Th17 ratio, relevant to the T1D disease process. In summary, we have preliminarily developed a new biohybrid system, associated with immunoregulatory properties, that is ready for in vivo application.Entities:
Keywords: Adult mesenchymal stem cell; HLAG-5; Immunomodulation; Microencapsulation; Proliferation inhibition; Type 1 diabetes mellitus
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Year: 2015 PMID: 26680606 DOI: 10.1016/j.clim.2015.12.002
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969