Table 2.
System | Indication | Sample size | Cell type | Study design | Delivery route | Outcome | Ref | |
---|---|---|---|---|---|---|---|---|
| ||||||||
Non-Skeletal | Cardiovascular | Acute myocardial infarction | 34\35 | Allogenic MSCs | Placebo controlled clinical trial | Intracoronary | Increased left ventricular ejection fraction and left ventricular end diastolic volume, improve contractility and enhanced infarct viability | 76 |
Acute myocardial infarction | 53 | Allogenic MSCs (Prochymal) | Double-blind, placebo-controlled | Intravenous | Significant improvement of ejection fraction in hMSC-treated group | 77 | ||
Nephrology | Acute kidney injury (post-operative) | 15 | Autologous MSCs | Phase 1 Trial | Intraarterial | Renal function was well preserved postoperatively, and none of the patients required hemodialysis. | 87 | |
Gastro-intestinal | Perianal fistulas (Crohn disease) | 24\25 | Allogenic adiposetissue MSCs | Phase II Randomized controlled trial | Intravenous | AD-MSC induced higher rates of healing when used together with fibrin glue compared to fibrin glue alone | 91 | |
Neurology | Multiple system atrophy | 11\18 | Autologous MSCs | case-control study | Intra-arterial × 1 Intravenous ×3 |
Delayed the progression of neurological deficits with achievement of functional improvement | 82 | |
Stroke | 16\36 | Autologous MSC | Randomised, Placebo controlled | Intravenous | Improve recovery after stroke, improvements in the Barthel index and modified Rankin score | 81 | ||
Multiple systems | Steroid-resistant, severe, acute GvHD | 55 | Autologous MSCs | phase II study | Intravenous | Better survival in patients with complete response (54.5%) | 68 | |
Acute GvHD | 32 | Allogenic MSCs | Randomized clinical trial | Intravenous | 77% of patients fully responded, 17% partially responded | 69 | ||
Lupus nephritis | 16 | Allogeneic umbilical cord MSCs | Phase I clinical trial | Intravenous | Improved Systemic activity Index and renal function | 95 |
Abbreviations: GvHD, Graft versus host disease. MSC’s, Mesenchymal Stem Cells. SLE, Systemic lupus erythromatosis