Abstract
Systemic lupus erythematosus (SLE) is a devastating autoimmune disease characterized by chronic inflammation and systemic destruction of host organs or tissue. A key feature of SLE is T cell dysfunction characterized by hyperresponsive antigen receptor signaling. In this issue of the JCI, McDonald and colleagues provide evidence that homeostasis of a subset of lipids, the glycosphingolipids (GSLs), is severely perturbed in the membranes of T cells from SLE patients. Furthermore, normalization of GSLs restored TCR signaling and ameliorated T cell dysfunction. These data suggest that targeting host metabolism may be an effective means of reinforcing selftolerance and attenuating autoimmunity. © Copyright 2014 American Society for Clinical Investigation.
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CITATION STYLE
Kidani, Y., & Bensinger, S. J. (2014, February 3). Lipids rule: Resetting lipid metabolism restores T cell function in systemic lupus erythematosus. Journal of Clinical Investigation. https://doi.org/10.1172/JCI74141
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