Clinical Trial of Autologous Dendritic Cell Administration Effect on Water Molecule Diffusion and Anti-Inflammatory

Paulus Stefanus Dimu1,2, Aziza Ghanie Icksan1, Farhat1

  • 1Faculty of Medicine, Dentistry, and Health Science, Universitas Prima Indonesia, Medan 20118, Indonesia.

PubMed

Insights

Autologous dendritic cell therapy for diabetic kidney disease showed potential gender-specific immune responses but limited overall biomarker improvements. Further research is needed to confirm its therapeutic value in managing kidney inflammation and function.

Area of Science:

  • Nephrology
  • Immunology
  • Biomedical Engineering

Background:

  • Diabetic kidney disease (DKD) is a major cause of mortality, linked to chronic inflammation.
  • Transforming growth factor-β (TGF-β) and intracellular adhesion molecule-1 (ICAM-1) are key inflammatory markers in kidney damage.
  • Understanding inflammation's role is crucial for developing effective DKD treatments.

Purpose of the Study:

  • To investigate the impact of autologous dendritic cell therapy on inflammation and kidney function in DKD patients.
  • To assess changes in apparent diffusion coefficient (ADC), TGF-β, and ICAM-1 levels post-intervention.
  • To explore potential gender-specific responses to the therapy.

Main Methods:

  • A quasi-experimental clinical trial involving 22 DKD patients.
  • Administration of autologous dendritic cell injections.
  • Assessment of ADC via MRI, and analysis of TGF-β and ICAM-1 serum levels before and after treatment.

Main Results:

  • Median ADC showed an insignificant decrease (1.75 to 1.64 mm²/s, p=0.223).
  • ICAM-1 levels significantly increased in females (p=0.04) but not males (p=0.35).
  • No significant changes in TGF-β levels (p=0.506); ADC changes did not correlate with CKD severity.

Conclusions:

  • Autologous dendritic cell therapy may elicit gender-specific immune responses in DKD patients.
  • The therapy demonstrated limited overall improvement in key biomarkers.
  • Further research is warranted to validate the therapeutic potential and understand gender-specific effects.