Abstract
It has been difficult to develop therapies that target those T cells initiating and mediating the pathogenesis of autoimmune disease. Indeed, most current treatments indiscriminately affect both the autoreactive T cells and the "good" T cells, putting the patient at risk of compromised immune function. A new approach (see the related article beginning on page 969) raises the possibility of targeted therapy for autoimmunity. Transplantation of hematopoietic stem cells modified to express a protective form of MHC class II corrects a defect in central tolerance. This method contrasts with other targeted therapies that attempt to modify peripheral tolerance, which is also defective in type 1 diabetes mellitus.
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CITATION STYLE
Creusot, R. J., & Fathman, C. G. (2004). Gene therapy for type 1 diabetes: A novel approach for targeted treatment of autoimmunity. Journal of Clinical Investigation. The American Society for Clinical Investigation. https://doi.org/10.1172/JCI23168
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