Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters








Database
Publication year range
2.
Diabetes Metab ; 35(2): 85-93, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19230736

ABSTRACT

Mesenchymal stem cells (MSCs) are multipotent non-haematopoietic progenitor cells that are being explored as a promising new treatment for tissue regeneration. Although their immunomodulatory properties are not yet completely understood, their low immunogenic potential together with their effects on immune response make them a promising therapeutic tool for severe refractory autoimmune diseases. Type 1 diabetes is characterized by T cell-mediated autoimmune destruction of pancreatic beta cells. While insulin replacement represents the current therapy for type 1 diabetes, its metabolic control remains difficult, as exogenous insulin cannot exactly mimic the physiology of insulin secretion. Pancreatic or islet transplantation can provide exogenous insulin independence, but is limited by its intrinsic complications and the scarcity of organ donors. In this context, stem cell therapy, based on the generation of insulin-producing cells (IPCs) derived from MSCs, represents an attractive possibility. In this review, we provide a brief characterization of MSC immunomodulatory effects, and present the current experimental evidence for the potential therapeutic efficacy of MSC transplantation in diabetes.


Subject(s)
Diabetes Mellitus, Type 1/therapy , Insulin-Secreting Cells/cytology , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells/physiology , Animals , Cell Differentiation , Disease Models, Animal , Humans , Immunosuppression Therapy , Insulin-Secreting Cells/physiology , Mesenchymal Stem Cells/immunology
3.
Rev Med Interne ; 30(3): 287-99, 2009 Mar.
Article in French | MEDLINE | ID: mdl-18930338

ABSTRACT

Mesenchymal stem cells (MSC) represent a population of the bone marrow microenvironment, which participates in the regulation of haematopoietic stem cells (HSC) self-renewal and differentiation. MSC are multipotent non-haematopoietic progenitors, which have been explored as a promising treatment in tissue regeneration. Both in vitro and in vivo, the MSC inhibit the T, B, NK and dendritic cell functions. Although MSC immunomodulating properties are not yet completely understood, their low immunogenic potential can be used as a therapeutic tool not only for regenerative medicine, but also for the treatment of graft-versus-host disease (GVHD) after bone marrow transplantation as well as for specific cases of severe refractory autoimmune diseases. Experimental and clinical data gave encouraging results, showing that MSC injection allowed controlling refractory GVHD, restoring bone development in children with osteogenesis imperfecta or improving heart function after myocardial infarction. Phase I-II studies are in progress in various countries to investigate the potential benefit from MSC due to their immunosuppressive properties, as an adjunctive therapy for severe refractory autoimmune disease.


Subject(s)
Autoimmune Diseases/therapy , Immunosuppression Therapy , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells , Adult , Animals , Arthritis, Rheumatoid/therapy , Bone Marrow Transplantation/immunology , Cell- and Tissue-Based Therapy , Cells, Cultured , Child , Clinical Trials as Topic , Clinical Trials, Phase I as Topic , Clinical Trials, Phase II as Topic , Disease Models, Animal , Graft vs Host Disease/therapy , Humans , Lupus Erythematosus, Systemic/therapy , Mesenchymal Stem Cells/immunology , Mesenchymal Stem Cells/physiology , Mice , Mice, Inbred NOD , Multiple Sclerosis/therapy , Myocardial Infarction/therapy , Osteogenesis Imperfecta/therapy , Papio , Prospective Studies , Scleroderma, Systemic/therapy
SELECTION OF CITATIONS
SEARCH DETAIL