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Intra-articular adipose-derived cell therapies reduce pain and improve function in knee osteoarthritis without serious adverse events.

Intra-articular adipose-derived cell therapies reduce pain and improve function in knee osteoarthrit…
Photo by National Cancer Institute / Unsplash
Key Takeaway
Consider intra-articular adipose-derived cell therapies for pain relief in knee osteoarthritis, noting limited structural regeneration evidence.

This systematic review and meta-analysis evaluated the efficacy and safety of intra-articular adipose-derived cell therapies, including adipose-derived stem cells, stromal vascular fraction, and mesenchymal fraction adipose tissue, for treating knee osteoarthritis in adults. The analysis included nineteen randomized controlled trials comparing these interventions against placebo, hyaluronic acid, platelet-rich plasma, corticosteroids, or conservative care.

The authors observed that these therapies resulted in clinically meaningful reductions in pain and improvements in functional outcomes compared to comparators. Favorable magnetic resonance imaging findings were noted, indicating improvements in cartilage quality, although the data did not demonstrate consistent cartilage regeneration. Symptomatic benefits of mesenchymal fraction adipose tissue were found to be comparable to established injective therapies.

Regarding safety, no serious treatment-related adverse events were reported across the included studies, suggesting a tolerable safety profile. However, the authors highlight limitations including the lack of consistent cartilage regeneration and heterogeneous results among mesenchymal fraction adipose tissue trials. Consequently, the practice relevance suggests these therapies are safe and provide meaningful relief for selected patients, with adipose-derived stem cells showing the most consistent clinical signals.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Knee osteoarthritis is a leading cause of chronic pain, functional limitation, and disability worldwide, imposing a substantial socioeconomic burden. Despite advances in conservative management and intra-articular therapies, many patients experience limited or transient symptomatic relief, underscoring the need for biologically based interventions. Intra-articular adipose-derived cell therapies, including adipose-derived mesenchymal stem or stromal cells (ADSCs), stromal vascular fraction (SVF), and microfragmented adipose tissue (MFAT), have emerged as regenerative strategies aimed at modulating inflammation and joint homeostasis. This systematic review evaluated the efficacy, structural effects, and safety of intra-articular adipose-derived cell–based therapies for knee osteoarthritis in adults. Randomized controlled trials published between 2015 and 2025 were identified through systematic searches of PubMed, Embase, Scopus, and Web of Science. Eligible studies compared ADSCs, SVF, or MFAT with placebo, hyaluronic acid, platelet-rich plasma, corticosteroids, or conservative care, and reported outcomes on pain, function, imaging-based structural changes, and safety. Nineteen randomized controlled trials met inclusion criteria. Across studies, adipose-derived interventions, particularly ADSC-based therapies, produced clinically meaningful reductions in pain and improvements in functional outcomes assessed by WOMAC, KOOS, and visual analog scales. Several ADSC and SVF trials reported favorable magnetic resonance imaging findings, including improvements in cartilage quality, although consistent cartilage regeneration was not demonstrated. MFAT trials yielded heterogeneous results, often showing symptomatic benefits comparable to established injective therapies but limited structural effects. No serious treatment-related adverse events were reported. Intra-articular adipose-derived cell therapies are safe and provide meaningful pain relief and functional improvement in selected patients, with ADSCs showing the most consistent clinical signals. https://www.crd.york.ac.uk/PROSPERO/view/CRD420251241498, Identifier: CRD420251241498.
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