Abstract
Objective
To investigate the clinical efficacy and underlying mechanisms of mesenchymal stromal cell (MSC) therapy in systemic sclerosis (SSc).
Methods
We prospectively evaluated the efficacy of MSC therapy in SSc patients. To elucidate the therapeutic mechanisms, we integrated paired multi‐omics data: proteomics (n=7), metabolomics (n=7), and both bulk (n=6) and single‐cell (n=2) RNA‐seq. Baseline disease‐associated signatures were mainly defined by publicly available datasets of peripheral blood mononuclear cells (PBMCs, 21 SSc vs. 6 healthy donors).
Results
MSC therapy significantly ameliorated skin fibrosis (median mRSS decrease 7.0 [IQR, 3.8–9.3],
P
P
adj
P
adj
P
adj
Conclusions
Our study underscores the MSC‐mediated immunometabolic reprogramming to restore immune homeostasis by targeting upstream OXPHOS defects of cDC2s in SSc.
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