81172068 P- Reviewer: Bellanti F, Hann HW, Morioka

D S- E

81172068 P- Reviewer: Bellanti F, Hann HW, Morioka

D S- Editor: Song XX L- Editor: Wang TQ E- Editor: Lu YJ
Core tip: Autoimmune diseases affect approximately 5% of the human population, leading to serious disability and effective methods to treat these diseases are still not perfect. Mesenchymal stem Caspase pathway cells (MSCs) are assumed to be promising agents, both for regenerative medicine and cell therapy for autoimmune disorders. Under the influence of some factors, mesenchymal stem cells secrete cytokines which induce suppression of the immune response. Studies on the secreted cytokines and the precise mechanisms involved in these suppressive mechanisms would create possibilities for efficient application of MSCs as a therapeutic means for treatment of autoimmune diseases. INTRODUCTION Maintenance of immunological self-tolerance and immune homeostasis in the organism is under the control of a complex and sophisticated process of immunoregulation and its dysfunction could be a critical factor in the development of autoreactive and potentially life-threatening conditions. Profound understanding of the precise mechanisms underlying this immunoregulatory process could lay the ground to develop a more suitable and efficient therapy for autoimmune diseases. Regulation

of the immune response by mesenchymal stem cells (MSCs) is mediated by a number of cell subtypes and secreted factors and recently new cell-based therapeutic approaches have emerged as successful strategies for treatment of various inflammatory and autoimmune conditions. In the last decades, mesenchymal stem cells, one type of adult stem cells, have gained considerable interest as extremely promising cell therapeutic

agents[1,2] due to their unique combination of immunomodulatory properties and self-renewal and multilineage differentiation capacity[3,4]. MSCs have been shown to exert profound anti-inflammatory and immunomodulatory effects on almost all the cells of the innate and adaptive Carfilzomib immune systems via a variety of mechanisms, notably cytokine and chemokine secretion[5]. Mesenchymal stem cells are a population of undifferentiated multipotent adult stem cells that naturally reside within the human body and are generally defined as plastic-adherent, fibroblast-like cells possessing extensive self-renewal properties and potential to differentiate in vitro and in vivo into a variety of mesenchymal lineage cells[4,6]. MSCs were initially described in the bone marrow by Friedenstein et al[7,8] as a small subpopulation of colony-forming unit fibroblasts which could be distinguished from the rest of the bone marrow cells on the basis of their plastic adherence, spindle-shaped appearance and rapid expansion[7].

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