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Editorial
©Author(s) (or their employer(s)) 2026.
World J Stem Cells. Feb 26, 2026; 18(2): 114303
Published online Feb 26, 2026. doi: 10.4252/wjsc.v18.i2.114303
Table 1 Minimum reporting set for intra-articular extracellular vesicle studies (bench and early clinical)
Domain
Required elements (minimum)
How to report (units/assays)
Harmonized time-points
Quality/acceptance notes
EV identity & purityParticle size/number; protein; ≥ 1 positive and ≥ 1 negative protein markerNTA (particles/mL); BCA or Simoa (μg/mL); western/flow for tetraspanins; negative marker (e.g., calnexin)N/AFollow MISEV2023 identity/purity panels; disclose isolation workflow and co-isolates
Dose normalizationReport both particle number and protein massPer-joint dose: Total particles and μg; lot-to-lot CVsN/ADual metrics enable cross-study comparison and QC trending
Exposure/retention (biodistribution)Joint residence and/or tissue associationFluorescent or radiolabel tracking; cargo-based tracers (qPCR/protein)1 hour, 24 hours, 7 days (shared anchors)Predefine quench/correction; report synovial fluid/tissue ROIs and decay characteristics
Potency/MoA-linked readoutMechanism-aligned assay + viability/toxicityCell-based PD (e.g., PINK1/PRKN index), live/dead, cytokinesN/ASpecify acceptance ranges; link potency to dose and exposure
Transparency & rigorProtocol registration; method completenessEV-TRACK/EV-METRIC ID; checklist linkN/AImproves reproducibility and peer auditability
SafetyLocal/systemic AEs; labsJoint flare, effusions, vitals; CRP; imaging if indicatedVisit-aligned (e.g., baseline, week 2, week 12)IND oversight where applicable; note no FDA-approved EV products


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