A Pilot Study of Mesenchymal Stem Cell Therapy for Acute Liver Allograft Rejection
Autor: | Xi Yu, Ying Wang, Min Zhang, Lingzhan Meng, Zhenwen Liu, Haibin Su, Ming Shi, Lei Jin, Fu-Sheng Wang, Rounan Xu, Yan-ling Sun, Hongbo Wang |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Graft Rejection Male medicine.medical_specialty medicine.medical_treatment Cell Pilot Projects Liver transplantation Human Clinical Articles Mesenchymal Stem Cell Transplantation Gastroenterology Umbilical cord T-Lymphocytes Regulatory Dinoprostone 03 medical and health sciences 0302 clinical medicine Human Clinical Article Transforming Growth Factor beta Internal medicine medicine Humans Clinical Trials Prostaglandin E2 Aged biology business.industry Mesenchymal stem cell Histology Mesenchymal Stem Cells Cell Biology General Medicine Transforming growth factor beta Middle Aged Adult Stem Cells 030104 developmental biology medicine.anatomical_structure 030220 oncology & carcinogenesis biology.protein Acute rejection Th17 Cells Female Stem cell business Developmental Biology medicine.drug |
Zdroj: | Stem Cells Translational Medicine |
ISSN: | 2157-6580 2157-6564 |
Popis: | Acute allograft rejection remains common after liver transplantation despite modern immunosuppressive agents. In addition, the long-term side effects of these regimens, including opportunistic infections, are challenging. This study evaluated the safety and clinical feasibility of umbilical cord-derived mesenchymal stem cell (UC-MSC) therapy in liver transplant patients with acute graft rejection. Twenty-seven liver allograft recipients with acute rejection were randomly assigned into the UC-MSC infusion group or the control group. Thirteen patients received one infusion of UC-MSCs (1 × 106/kg body weight); one patient received multiple UC-MSC infusions; 13 patients were used as controls. All enrolled patients received conventional immunosuppressive agents with follow-up for 12 weeks after UC-MSC infusions. No side effects occurred in treated patients. Four weeks after UC-MSC infusions, alanine aminotransferase levels had decreased markedly and remained lower throughout the 12-week follow-up period. Importantly, allograft histology was improved after administration of UC-MSCs. The percentage of regulatory T cells (Tregs) and the Treg/T helper 17 (Th17) cell ratio were significantly increased 4 weeks after infusions; in contrast, the percentage of Th17 cells showed a decreasing trend. In controls, the percentages of Tregs and Th17 cells and the Treg/Th17 ratio were statistically unchanged from the baseline measurements. Transforming growth factor beta 1 and prostaglandin E2 were increased significantly after UC-MSC infusions; by contrast, there were no significant changes in controls. Our data suggest that UC-MSC infusion for acute graft rejection following liver transplantation is feasible and may mediate a therapeutic immunosuppressive effect. |
Databáze: | OpenAIRE |
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