BPG is committed to discovery and dissemination of knowledge
Review
Copyright: ©Author(s) 2026.
World J Stem Cells. Oct 26, 2026; 18(10): 124937
Published online Oct 26, 2026. doi: 10.4252/wjsc.124937
Table 1 The clinical trials using stem cells in the treatment of type 1 diabetes
Ref.
Year
Type of SCs
No.
HbA1c
TIR
Fasting C-peptide
Postprandial C-peptide
Insulin dose
[15]2021hESCs15< 7% over all follow-upIncreasedbIncreasedaBoth glucose and meal-responsive C-peptide increasedaDecreasedb (1/15 patients decreased of 50%)
[16]2025hiPSCs14< 7% after 120 days, decreased by 1.81 percentage points at 1 year (7.8% at baseline)> 70% at day 150, increased by 44.4 percentage points at day 365 (49.5% to 93.9%)Detected at day 90 (undetectable at baseline)With an average value of 424 pmol/L at day 90 and
1274 pmol/L at day 365 (undetectable at baseline)
The average insulin dose decreased by 92%; 10/12 patients achieved insulin independence and did not resume through day 365; insulin dose was decreased for 2/12 patients
[17]2024hiPSCs1Decreased by 1.07 percentage points at day 75 (7.57% to 6.50%) and then remained within the non-diabetic range (< 5.7%)Increased by 55.41 percentage points (43.18% to 98.59%)Increased to 102.6 pmol/L after 1 week; increased to a plateau after achieving insulin independence, with a fluctuation range of 407.1 to 721.6 pmol/L (undetectable at baseline)Increased by 20% over fasting on day 56; further improved to 834.1 pmol/L at day 120 (undetectable at baseline)Began to decline after 2 weeks; achieved complete insulin independence on day 75 and remained so during the 1-year follow-up
[25]2015Autologous BM-MSCs9No significant difference between the MSC group and control groupNo significant difference between the MSC group and control groupMaintained in 6/9 patients of the MSC group, but decreased in 8/9 patients in the control groupNo significant difference between MCS and control groups
[26]2022Autologous BM-MSCs11Decreased by 1.46 percentage points compared with the control group at 1 yeara; the early treatment group had a significant reduction of 2.95b, 1.69a, and 1.40a percentage points relative to the late treatment group at 3, 6, and 9 months, respectivelyHigher than that in the control group, but with no significant difference; the early treatment group had a significant increase of 0.58 ng/mLa, 0.46 ng/mLa, and 0.56 ng/mLa than the late treatment group at 3, 6, and 9 months, respectivelyHigher than that in the control group, but with no significant differenceIncreased in both groups, with no significant difference between two groups
[19]2013Allogeneic WJ-MSCs15Decreased by 1.3 percentage points (the lowest level) at month 6 (6.8% ± 0.57% to 5.5% ± 0.67%) and maintained a small fluctuation over the following 18 monthsHigher than the control group, also higher than the baseline at the end of follow-up, whereas the control group showed a gradual downward trend3/15 patients discontinued insulin; daily insulin dose was reduced by more than 50% in 8 patients and by 15%-50% in 1 patient
[27]2016Allogeneic BM-MSCs5 (1 patient was lost to follow-up)3/4 patients maintained a similar or lower level for at least 3 yearsDeclined slowly in all patients1 patient rose above the baseline for as long as 1 yearInsulin dose was reduced by 50% in 2/4 patients; 1 patient achieved insulin independence for 3 months
[28]2022Allogeneic UC-MSCs and BM-MSCs14 (4 of BM-MSCs, 10 of UC-MSCs)Decreased both in BM-MSC and UC-MSC groups, while slightly increased in the control groupa; no significant difference in the reduction between BM-MSCs and UC-MSCs groupClinical remission (10% increase from baseline in the fasting C-peptide and/or postprandial C-peptide levels) was achieved in 4/14 patientsc, including 1 patient (1/4, 25.0%) in the BM-MSC group and 3 patients (3/10, 33.3%) in the UC-MSC groupcReduced relative to the control groupa; no significant difference in the reduction between BM-MSC and UC-MSC groups
[29]2020Allogeneic AD-MSCs8Lower than control group (6.47% ± 0.86% vs 7.48% ± 0.52%)aNo significant difference between the MSC and control groupsNo significant difference between the MSC and control groupsLower than control group (0.25 ± 0.19 IU/kg vs 0.56 ± 0.23 IU/kg)a; 2/8 patients achieved insulin independence for 4 and 8 weeks, respectively
[30]2015Autologous/allogeneic
AD-MSCs with hematopoietic stem cells
10 of autologous, 10 of allogeneicDecreased in both groups with no significant differenceIncreased in both groups; higher in the autologous group than in the allogeneic group (0.93 ± 0.24 ng/mL vs 0.46 ± 0.29 ng/mL)aThe mean insulin dose decreased by 37.93% in the autologous group and by 33.11% in the allogeneic group
Table 2 The clinical trials using stem cells in the treatment of type 2 diabetes
Ref.
Year
Type of SCs
No.
HbA1c
TIR
Fasting C-peptide
Postprandial C-peptide
Diabetic medication dose
Other indicators
[33]2017Autologous BM-MSCs106/10 patients reduced below 7%, but no significant improvement relative to baseline No significant improvement relative to baselineNo significant improvement relative to baseline6/10 patients achieved a > 50% reduction in insulin dose relative to baselineISI: Had a significant improvement (0.1 to 0.4 μmol/kg/minute/pmol/L)a
[34]2021Autologous BM-MSCs30Patients with duration of < 10 years and a BMI of < 23 kg/m2 showed a reduction of 0.7 percentage points (from 8.9% ± 1.6% to 8.2% ± 0.5%)a; no significant change (even increase) in patients with duration of > 10 yearsPatients with duration of < 10 years and a BMI of < 23 kg/m2 showed a slight decreasec, whereas those with duration of > 10 years showed a significant declinea2/4 patients using only insulin had an average reduction of 6 IU/day; 5/10 patients using multiple drugs had an average reduction of 868 mg/day; 1/3 patients using insulin and a single drug had a decrease in drug dose but an increase in insulin dose; 8/11 patients using insulin and multiple drugs: 5 of these 8 patients showed reduced use of oral drugs, and 2 patients had a decreased insulin dose
[35]2011Allogeneic PD-MSCs10Decreased by 3.1 percentage points (9.8% to 6.7%)aIncreased by 34.62% (2.6 ± 2.1 ng/mL to 3.5 ± 2.3 ng/mL)aIncreased by 31.71% (5.6 ± 4.0 ng/mL to 8.2 ± 3.9 ng/mL)aDecreased by 45.53% (63.7 ± 18.7 to 34.7 ± 13.4 IU)a; insulin dose was reduced for 4/10 patients by > 50%
[36]2014Allogeneic WJ-MSCs22Decreased by 1.2 percentage points (8.20% ± 1.69% to 7.0% ± 0.60%)aIncreased to the peak value at month 6 (1.95 ± 1.3 ng/mL, increased by 51.16%)a, followed by slight decrease at month 12 (1.86 ± 1.0 ng/mL, which still represents 44.19%a increase relative to baseline (1.29 ± 0.83 ng/mL)No significant difference compared to baseline(1) 16/17 patients using insulin had a dose reduction of 53.06% (0.49 ± 0.22 to 0.23 ± 0.19 IU/kg/day)a, 7 patients achieved insulin independence, which was maintained until the last follow-up; 5 patients had a dose reduction of ≥ 50%; and (2) 1/5 patients using drugs became completely drug-free, which was maintained until the last follow-up, 4/5 had a dose reduction of > 50HOMA-2B: Increased by 49.81%a at month 6 (98.86% ± 43.91%) and 30.32%a at month 12 (86.0% ± 37.1%) (65.99% ± 23.49% at baseline)
[37]2022Allogeneic UC-MSCs45Decreased 1.5 percentage points (9.02% ± 1.27% to 7.52% ± 1.07%)a in the UC-MSC group, and 0.7 percentage points in the control group (8.89% ± 1.11% to 8.19% ± 1.02%)c; with a significant difference noted between the two groupsaNo significant increase compared with the baseline (2.01 ± 0.70 to 2.07 ± 0.70 ng/mL)c; no significant difference between the two groups eitherNo significant change compared with the baseline (1.94 ± 0.61 to 1.92 ± 0.53 ng/mL)c; no significant difference between the two groups eitherThe percentage of insulin reduction was significantly higher in the UC-MSC group than in the control group (27.78% vs 15.62%)aGIR: Increased by 52.56% in the UC-MSC group (3.12 to 4.76 mg/minute/kg)a, but no significant change was noted in the control group (3.26 to 3.60 mg/minute/kg)c; a significant difference was noted between the two groupsa
[38]2024hiPSCs1Decreased by 2.0 percentage points (6.6% to 4.6%)(Target range: 3.9-10 mmol/L) increased by 12.3 percentage points (87.7% to 100%)Increased to a peak of 1.09 nmol/L at week 24 (increased by 374%, 0.23 nmol/L at baseline) and then decreased but remained within the normal rangeAUC·180 minutes of C-peptide: Increased by 49.64% (246.8 to 369.3 nmol/L)Insulin and oral medications were discontinued at week 11 and 56, respectively, and were maintained until the last follow-upTITR (target range: 3.9-7.8 mmol/L): Increased by 43.3 percentage points (56.7% to 100%)


Write to the Help Desk