Kabelitz Dieter, Geissler Edward K, Soria Bernat, Schroeder Insa S, Fändrich Fred, Chatenoud Lucienne
Institute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany.
Trends Immunol. 2008 Feb;29(2):68-74. doi: 10.1016/j.it.2007.11.001. Epub 2008 Jan 7.
Type 1 diabetes (T1D) is an autoimmune disease that results from the destruction of insulin-producing pancreatic islet cells owing to the aggressive effector function of autoreactive T cells. In addition to lifetime supply of exogenous insulin, whole-pancreas or islet transplantation is presently the only alternative therapy for severely ill patients. Here, we discuss the current status of the development of cell-based therapies that are based on essentially two options, i.e. replacement of islet cells by islet-like cells derived from embryonic or adult stem cells, and re-establishment of immunological tolerance to islet self-antigens through regulatory T cells and/or tolerance-promoting monocyte-derived cells. A combination of both approaches will be required to turn cell-based therapy of T1D into clinical success.
1型糖尿病(T1D)是一种自身免疫性疾病,由于自身反应性T细胞的强烈效应功能,导致产生胰岛素的胰岛细胞被破坏。除了终身供应外源性胰岛素外,全胰腺或胰岛移植目前是重症患者的唯一替代疗法。在此,我们讨论基于细胞的疗法的发展现状,这些疗法主要基于两种选择,即通过源自胚胎或成体干细胞的类胰岛细胞替代胰岛细胞,以及通过调节性T细胞和/或促进耐受的单核细胞衍生细胞重建对胰岛自身抗原的免疫耐受。要使基于细胞的T1D治疗取得临床成功,需要将这两种方法结合起来。