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. 2024 Feb 29;102(4):537–570. doi: 10.1007/s00109-024-02432-w

Table 4.

Intravenous administration of allogeneic MSCs in DKD patients

MSC source Age DM type Sample Sample distribution No. of injections Injection method Results Phase Adverse events (n) Follow up (m) Ref
BM-MPC

Placebo: 74:8 ± 7:9 y,

Lower dose

MSCs: 70:5 ± 7:4 y

Higher dose

MSCs: 64:8 ± 10:1 y

T2DM 30 150 × 106/kg (lower dose) or 300 × 106/kg (higher dose) Single dose IV ↔ eGFR, albuminuria ↔ lipid profile ↔ blood pressure ↔ serum C-reactive protein, TNF-α ↓ serum IL-6 I/II None 12 [152]
BM-MSC Placebo: 54–66 y, ORBCEL-M: 66–73 y T2DM 16 ORBCEL-M (80 × 106 cells) Single dose IV

↔ eGFR,

↓ annual mGFR decline in groups

 ↔ UACR, ↔ Safety,

= blood glucose; HbA1c; serum total cholesterol; serum triglycerides; and serum C-reactive protein,

↑ sTNFR1, 1NGAL, sVCAM-1, Tregs

1b/IIa None 18 [153]

mGFR measured glomerulus filtration rate, Tregs regulatory T cells, sTNFR1 tumor necrosis factor receptor 1,NGAL neutrophil gelatinase-associated lipocalin, sVCAM-1 soluble vascular cell adhesion molecule 1, IV intravenous

↔ represents a no significant change or impact in either direction

↓ indicates a downward or decreasing effect

= represents stability as values or parameters remain unchanged or steady over time

↑ indicates increasing levels