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Characterization of intestinal immune responses in generalized human and murine lipodystrophy

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Item Type:Article
Title:Characterization of intestinal immune responses in generalized human and murine lipodystrophy
Creators Name:Letizia, Marilena, Omar, Toka, Weidner, Patrick, Jakob, Manuel O., Freise, Inka, Krug, Susanne M., Löscher, Britt-Sabina, Rosati, Elisa, Obermayer, Benedikt, Gamez-Belmonte, Reyes, Hecker, Julia, Ziegler, Jörn-Felix, Weixler, Benjamin, Asbach, Patrick, Kunkel, Desiree, Stumvoll, Michael, Miehle, Konstanze, Becker, Christoph, Klose, Christoph S.N., Glauben, Rainer, Beule, Dieter, Kühl, Anja A, Conrad, Thomas, Tacke, Frank, Wirtz, Stefan, Franke, Andre, Sanders, Ashley D., Siegmund, Britta and Weidinger, Carl
Abstract:Acquired generalized lipodystrophy (AGL) is a rare metabolic disorder frequently associated with autoimmunity. Its etiology is incompletely understood, and the effect of adipose tissue loss on intestinal inflammation in AGL remains unclear. Using mass cytometry and single-cell RNA-seq, we observed an oligoclonal expansion of T cells in the periphery and inflamed intestine in a patient with AGL and Crohn's disease (AGLCD). To explore if loss of adipose tissue triggers lymphoproliferation, we studied lipodystrophic mice as a model for AGL. Unexpectedly, lipodystrophic mice did not show T cell expansion, were protected from colitis, and displayed a defect in the development of proinflammatory T cells, which could be reversed by allogeneic fat transplantations, indicating that clonal T cell expansion in AGLCD is not primarily caused by lipodystrophy. Instead, gene sequencing revealed a T cell-intrinsic de novo neuroblastoma RAS viral oncogene homolog (NRAS) mutation, implicating somatic mosaicism as a facilitator of clonal T cell expansion and intestinal inflammation in AGLCD.
Keywords:Animal Disease Models, Crohn Disease, Intestines, Lipodystrophy, T-Lymphocytes, Animals, Mice
Source:Journal of Clinical Investigation
ISSN:0021-9738
Publisher:American Society for Clinical Investigation
Volume:136
Number:6
Page Range:e192322
Date:16 March 2026
Official Publication:https://doi.org/10.1172/jci192322
PubMed:View item in PubMed
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