# Clinical Trial: Effects of Autologous Dendritic Cell Administration on Renal Hemodynamics and Inflammatory Biomarkers in Diabetic Kidney Disease

**Authors:** Endang Drajat, Aziza Ghanie Icksan, Jonny Jonny, Aditya Pratama Lokeswara, Bhimo Aji Hernowo, Elvita Rahmi Daulay, Terawan Agus Putranto

PMC · DOI: 10.3390/diseases13040122 · Diseases · 2025-04-21

## TL;DR

This study shows that autologous dendritic cell therapy may improve kidney function in diabetic patients by reducing inflammation and fibrosis markers.

## Contribution

The study introduces autologous dendritic cell administration as a novel therapeutic approach for diabetic kidney disease.

## Key findings

- Autologous dendritic cell treatment significantly reduced PSV and increased EDV in DKD patients.
- TGF-β and MMP-9 levels showed a strong correlation, with reduced MMP-9 influence on TGF-β after treatment.
- Females and microalbuminuria patients showed significant improvements in renal hemodynamics.

## Abstract

Background: Diabetic kidney disease (DKD) is a significant risk factor for End-Stage Renal Disease, with a high global incidence and mortality rate. Hyperglycemia in DKD induces inflammation, contributing to glomerular hyperfiltration, fibrosis, and impaired renal function. Current therapies, including SGLT2 inhibitors, ACE inhibitors, and ARBs, show limited efficacy. Autologous dendritic cells (DCs) offer potential anti-inflammatory effects by reducing cytokine activity and fibrosis biomarkers. Methods: A quasi-experimental pretest–post-test design was conducted involving 29 DKD patients. Baseline blood and urine samples were collected for MMP-9, TGF-β, and Doppler ultrasound (PSV, EDV) measurements. The subjects received subcutaneous injections of autologous DCs, and follow-up measurements were conducted four weeks after treatment. The statistical analyses included paired t-tests, Wilcoxon signed-rank tests, and linear regression. Results: After treatment, there were a significant decrease in PSV (from 47.1 ± 23.87 cm/s to 27.85 ± 20.53 cm/s, p = 0.044) and a significant increase in EDV (from 13 ± 5.32 cm/s to 15.7 ± 12.55 cm/s, p = 0.039). A strong correlation was observed between the TGF-β and MMP-9 levels (p = 0.001). Linear regression analysis showed reduced MMP-9 influence on the TGF-β after treatment, suggesting potential fibrosis reduction. Gender and UACR subgroup analyses revealed significant PSV and EDV improvements in females and the microalbuminuria group. Conclusion: Autologous dendritic cell therapy significantly improved renal hemodynamics and showed potential to reduce fibrosis by modulating TGF-β and MMP-9 levels in DKD patients, warranting further investigation.

## Linked entities

- **Proteins:** MMP9 (matrix metallopeptidase 9), TGFB1 (transforming growth factor beta 1)
- **Diseases:** Diabetic kidney disease (MONDO:0005016), End-Stage Renal Disease (MONDO:0004375)

## Full-text entities

- **Genes:** MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}
- **Diseases:** Hyperglycemia (MESH:D006943), impaired renal function (MESH:D007674), DKD (MESH:D003928), fibrosis (MESH:D005355), End-Stage Renal Disease (MESH:D007676), Inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12025661/full.md

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Source: https://tomesphere.com/paper/PMC12025661