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Preliminary evidence of renal function improvement in chronic progressive kidney disease using autologous CD34+ cell
Takayasu Ohtake1,2,3, Tsutomu Sato4, Toshitaka Tsukiyama5
1Regenerative Medicine, The Center for Cell Therapy & Regenerative Medicine, Shonan Kamakura General Hospital, Kamakura 247-8533, Kanagawa, Japan.
Insights
Autologous CD34+ cell transplantation shows promise for progressive chronic kidney disease (CKD). This regenerative therapy improved kidney function markers and was safe in a small patient group, warranting further research.
Area of Science:
- Nephrology
- Regenerative Medicine
- Cell Therapy
Background:
- Progressive chronic kidney disease (CKD) lacks established treatments to reverse its course.
- Current therapeutic options for advanced CKD are limited, highlighting the need for novel approaches.
Purpose of the Study:
- To assess the safety and efficacy of autologous CD34+ cell transplantation in patients with progressive CKD.
- To evaluate the impact of CD34+ cell therapy on renal function decline.
Main Methods:
- Four patients with an estimated glomerular filtration rate (eGFR) of 15.0-28.0 mL/minute/1.73 m² received two infusions of autologous CD34+ cells into the renal arteries.
- Cell collection involved granulocyte colony-stimulating factor treatment followed by magnetic isolation of CD34+ cells.
- Safety and efficacy were monitored over a 6-month period.
Main Results:
- Three out of four patients demonstrated an improved eGFR slope (change from -1.36 to +0.22 mL/minute/1.73 m²/month).
- Significant improvements were observed in intrarenal resistive index (P=0.004) and shear wave velocity (P=0.04).
- One patient experienced transient fever and bone pain; no severe adverse events were reported.
Conclusions:
- Repetitive autologous CD34+ cell transplantation is a safe and feasible option for progressive CKD.
- The findings suggest potential efficacy of this regenerative cell therapy, meriting larger clinical trials.
- Further large-scale studies are necessary to confirm the therapeutic benefits of CD34+ cell transplantation in progressive CKD.
Background:
To date, no specific treatment has been established to reverse progressive chronic kidney disease (CKD).
Aim:
To evaluate the safety and efficacy of autologous CD34+ cell transplantation in CKD patients who exhibited a progressive decline in renal function.
Methods:
The estimated glomerular filtration rate (eGFR) at the beginning of the study was 15.0-28.0 mL/minute/1.73 m2. After five days of treatment with the granulocyte colony-stimulating factor, mononuclear cells were harvested and CD34+ cells were magnetically collected. CD34+ cells were directly injected into the bilateral renal arteries twice (at 0 and 3 months), and their safety and efficacy were evaluated for 6 months.
Results:
Four patients were enrolled and completed the study. Three of four patients showed improvement in eGFR slope (eGFR slope > 0 mL/minute/1.73 m2), with the monthly slope of eGFR (delta eGFR) changing from -1.36 ± 1.1 (pretreatment) to +0.22 ± 0.71 (at 6 months) mL/minute/1.73 m2/month (P = 0.135) after cell therapy. Additionally, intrarenal resistive index (P = 0.004) and shear wave velocity (P = 0.04) were significantly improved after cell therapy. One patient experienced transient fever after cell therapy, and experienced bone pain during granulocyte colony-stimulating factor administration. However, no severe adverse events were reported.
Conclusion:
In conclusion, our findings suggest that repetitive peripheral blood-derived autologous CD34+ cell transplantation into the renal arteries is safe, feasible, and may be effective for patients with progressive CKD. However, a large-scale clinical trial is warranted to validate the efficacy of repetitive regenerative cell therapy using autologous CD34+ cells in patients with progressive CKD.
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