Copyright
        ©The Author(s) 2022.
    
    
        World J Diabetes. Oct 15, 2022; 13(10): 835-850
Published online Oct 15, 2022. doi: 10.4239/wjd.v13.i10.835
Published online Oct 15, 2022. doi: 10.4239/wjd.v13.i10.835
            Table 1 Summary of clinical trials using mesenchymal stem cells in type 1 diabetes mellitus
        
    | Ref. | Patient characteristics | Treatment | Therapeutic outcomes | 
| Wu et al[105], 20221 | n = 14; aged 27-47 yr | Intrapancreatic: Allogeneic UC-MSC + autologous BM-MNC | Insulin independence: No | 
| China, 8 yr | Duration of T1DM: 10-24 yr | Insulin requirement: Improvement at 1 yr but no difference at 8 yr | |
| FCP and HbA1C: Significant improvement | |||
| Significantly lower occurrence of diabetic complications | |||
| Izadi et al[108], 2022 | n = 20; aged 8-40 yr | BM-MSC | Insulin independence: No | 
| Iran, 12 mo | Duration of T1DM: < 1 yr (n = 11) and > 1 yr (n = 9) | Insulin requirement, FCP, HbA1C: Significant improvement | |
| FCP (n = 11): 0.92 ± 0.57 ng/mL | Number of hypoglycemic events decreased | ||
| Patients with early onset of T1DM benefit more | |||
| Adverse effects: Possible mild injection site reactions | |||
| Lu et al[106], 2021 | n = 27; aged 8-55 yr | IV (2x): Allogeneic UC-MSC | Insulin independence: 3 subjects | 
| China, 12 mo | Median duration of T1DM: 2.3 mo | Insulin requirement, HbA1C: No improvement | |
| FCP: 100 pmol/L ( 0.3 ng/mL) | SCP: improved in adult-onset T1DM subgroup | ||
| Adverse effects: Mild fever | |||
| Dantas et al[103], 20212 | N = 7; Aged 16-35 yr | Allogenic AD-MSC + 2000 UI/d cholecalciferol | Insulin independence: 1 subject | 
| Brazil, 6 mo | Duration of T1DM: ≤ 4 mo | Insulin requirement: Stable at 6 mo | |
| FCP: 0.80 ± 0.38 ng/dL | FCP and HbA1C: Significant improvement | ||
| Adverse effects: Transient headache, mild local reactions, immediate tachycardia, thrombophlebitis + other mild effects | |||
| Araujo et al[102], 2020 | n = 8; aged 16-28 yr | Allogenic AD-MSC + 2000 UI/d cholecalciferol | Insulin independence: 2 subjects | 
| Brazil, 3 mo | Duration of T1DM: ≤ 4 mo | Insulin requirement, HbA1C: Decreased significantly at 3 mo | |
| FCP: Only initial improvements, with the same results at the 3-mo visit | |||
| Adverse effects: Transient headache, mild local reactions, immediate tachycardia, thrombophlebitis + other mild effects | |||
| Cai et al[104], 2016 | n = 21; aged 18-10 yr | Intra-pancreatic: Allogeneic UC-MSC + autologous BM-MNC | Insulin independence: No | 
| China, 12 mo | Duration of T1DM: 2-16 yr | Insulin requirement, HbA1C: Decreased significantly | |
| FCP: < 0.1 pmol/mL (< 0.3 ng/mL) | FCP: Markedly increased | ||
| Adverse effects: Transient abdominal pain, bleeding | |||
| Carlsson et al[107], 2015 | n = 9; aged 18-40 yr | IV: Autologous BM-MSC | Insulin independence: No | 
| Sweden, 12 mo | Duration of T1DM: < 3 wk | Insulin requirement, HbA1C, SCP: No significant improvement | |
| SCP: > 0.1 nmol/L (> 0.3 ng/mL) | Adverse effects: No | ||
| Thakkar et al[100], 2015 | n = 20; aged 8-45 yr | Into portal + thymic circulation and subcutaneous tissue: | Insulin independence: No | 
| India, 24 mo | Duration of T1DM: > 12 mo | Insulin requirement: Decreased | |
| 2 groups with a mean C-peptide: | Group 1: Autologous IS-AD-MSC+ HSC | HbA1C, C-peptide: Sustained improvement | |
| Group 1: 0.22 ng/mL | Group 2: Allogeneic IS-AD-MSC+ HSC | Adverse effects: No | |
| Group 2: 0.028 ng/mL | |||
| Dave et al[101], 20153 | n = 10; aged 9-29 yr | Into portal + thymic circulation and subcutaneous tissue: autologous IS-AD-MSC+ HSC | Insulin independence: No | 
| India, 27 mo | Duration of T1DM: 2-15 yr | Insulin requirement: Decreased | |
| Pre-IV C-peptide: 0.22 ng/mL | HbA1C, C-peptide: Sustained improvement + significantly lower GADA levels | ||
| Adverse effects: No | |||
| Hu et al[99], 2013 | n = 15; aged < 25 yr | IV (2x): Allogeneic WJ-MSC | Insulin independence: 3 subjects | 
| China, 24 mo | Duration of T1DM: < 6 mo | Control group: normal saline | Insulin requirement: 8 patients more than 50% reduction | 
| C-peptide: ≥ 0.3 ng/mL | HbA1C: Significantly decreased; FCP: Significantly increased | ||
| Adverse effects: No | 
- Citation: Nagy G, Szekely TE, Somogyi A, Herold M, Herold Z. New therapeutic approaches for type 1 diabetes: Disease-modifying therapies. World J Diabetes 2022; 13(10): 835-850
- URL: https://www.wjgnet.com/1948-9358/full/v13/i10/835.htm
- DOI: https://dx.doi.org/10.4239/wjd.v13.i10.835

 
         
                         
                 
                 
                 
                 
                 
                         
                         
                        