Umbilical cord mesenchymal stem cell-derived secretome as a potential treatment for systemic lupus erythematosus: A double-blind randomized controlled trial

Authors

  • Arief Nurudhin Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia; Division of Rheumatology, Department of Internal Medicine, Dr. Moewardi General Hospital, Surakarta, Indonesia
  • Yulyani Werdiningsih Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia; Division of Rheumatology, Department of Internal Medicine, Dr. Moewardi General Hospital, Surakarta, Indonesia https://orcid.org/0000-0002-4116-5851
  • Indrayana Sunarso Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia; Division of Rheumatology, Department of Internal Medicine, Dr. Moewardi General Hospital, Surakarta, Indonesia https://orcid.org/0009-0000-3369-1766
  • Sri Marwanta Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia
  • Aritantri Damayani Division of Gastroenterohepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia
  • Nurhasan A. Prabowo Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia; Department of Internal Medicine, Universitas Sebelas Maret Hospital, Surakarta, Indonesia https://orcid.org/0000-0003-2016-5649
  • Andri Affandi Department of Internal Medicine Program, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia
  • Itqan Gazali Department of Internal Medicine, Universitas Sebelas Maret Hospital, Surakarta, Indonesia https://orcid.org/0009-0005-2383-3886
  • Ayu SI. Safitri Department of Internal Medicine, Universitas Sebelas Maret Hospital, Surakarta, Indonesia
  • Brigitte RA. Sidarta Department of Clinical Pathology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia

DOI:

https://doi.org/10.52225/narra.v5i1.1799

Keywords:

Systemic lupus erythematosus, lupus, MEX-SLEDAI, secretome, mesenchymal stem cell

Abstract

Umbilical cord mesenchymal stem cell-derived (UCMSC-derived) secretome is anti-apoptotic, anti-inflammatory, antifibrotic, angiogenic, and tissue-regenerating. Thus, it may treat systemic lupus erythematosus (SLE). The aim of this study was to investigate the impact of the UCMSC-derived secretome on SLE patients' disease activity, using Mexican systemic lupus erythematosus disease activity index (MEX-SLEDAI) score, complement (C3 and C4) levels, tumor necrosis factor-alpha (TNF-α), anti-double-stranded DNA (anti-dsDNA), and interleukin-6 (IL-6) levels. This double-blind randomized controlled trial investigated the efficacy and safety of UCMSC-derived secretome in SLE patients with moderate disease activity. A total of 29 female patients were randomized into two groups to receive weekly 1.5 cc intramuscular injections of UCMSC-derived secretome or placebo (0.9% NaCl) for six weeks. Disease activity was assessed using the MEX-SLEDAI score, C3 and C4 levels, pro-inflammatory cytokines (IL-6 and TNF-α), and anti-dsDNA antibodies at baseline, Day 22, and Day 43. Results showed a significant reduction in MEX-SLEDAI scores in the secretome group compared to the placebo group (p<0.05). Complement C3 levels significantly increased in the secretome group on Day 43, indicating improved immune homeostasis, while C4 levels did not show significant differences between groups. IL-6 and TNF-α levels showed decreasing trends in the secretome group. Anti-dsDNA levels exhibited a decreasing trend in the secretome group, though not statistically significant. Importantly, no severe adverse events were observed, underscoring the safety of the intervention. UCMSC-derived secretome demonstrated immunomodulatory and anti-inflammatory effects, reducing disease activity in SLE patients. These findings suggest its potential as a safe and effective adjunct therapy for SLE, although further studies with larger sample sizes and extended follow-up periods are needed to validate these results.

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