MSC Paracrine Signaling in Inflammatory Arthritis
Analysis of preclinical studies: MSC‑derived exosomes reduce synovial inflammation and joint damage.
ReadReviewing published research on mesenchymal stem cell paracrine signaling, T‑cell regulation, and anti‑inflammatory mechanisms applied to rheumatoid arthritis, lupus, multiple sclerosis, Crohn's disease, and other autoimmune disorders.
This article synthesizes findings from preclinical models and early‑phase clinical studies examining the use of MSCs as an immunomodulatory adjunct in autoimmune conditions. Emphasis is placed on paracrine mechanisms (IL‑10, TGF‑β, exosomes), Treg expansion, and reported safety profiles in rheumatoid arthritis, systemic lupus erythematosus, and inflammatory bowel disease.
Access reviewAnalysis of preclinical studies: MSC‑derived exosomes reduce synovial inflammation and joint damage.
ReadCase series and early trials report Treg restoration and reduced autoantibody titers; controlled studies ongoing.
ReviewCurrent evidence from phase I/II trials demonstrates that MSCs modulate microglial activation and promote neuroprotection; symptomatic benefit under investigation.
ExploreSystematic review highlights limited low‑bias evidence; local MSC administration shows safety and can achieve fistula closure in refractory cases.
SynopsisPreclinical models show reduced lymphocytic infiltration and improved glandular function; human trials warranted.
AbstractEarly clinical evidence: immunomodulation can slow C‑peptide decline; large RCTs needed.
ReadParacrine signaling reduces synovitis.
Treg restoration and safety data.
Neuroinflammation modulation.
Adjunctive MSC safety review.
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