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Updated: Jun 24, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
[NETosis in lupus nephritis].
T M Reshetnyak1,2, K S Nurbaeva1,2, I V Ptashnik3
1Nasonova Research Institute of Rheumatology.
Elevated levels of myeloperoxidase-DNA (MPO-DNA) complex were found in 39% of patients with systemic lupus erythematosus (SLE). This MPO-DNA complex is associated with lupus nephritis (LN) activity and renal damage in SLE patients.
Area of Science:
- Immunology
- Rheumatology
- Nephrology
Background:
- Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with potential organ damage.
- Lupus nephritis (LN) is a severe manifestation of SLE, impacting kidney function.
- Myeloperoxidase (MPO) is an enzyme released during neutrophil activation, and MPO-DNA complexes are markers of NETosis.
Purpose of the Study:
- To evaluate MPO-DNA complex levels in SLE patients.
- To assess the association between MPO-DNA complex levels and the presence and activity of LN.
Main Methods:
- Serum MPO-DNA complex levels were measured using ELISA in 77 SLE patients and 20 healthy controls.
- SLE patients included those with and without anti-phospholipid syndrome (APS).
- Associations with LN history, active LN, urinalysis findings, and SLEDAI-R were analyzed.
Main Results:
- SLE patients exhibited significantly higher MPO-DNA complex levels than controls (p=0.001).
- Elevated MPO-DNA complex levels were associated with a history of LN (p=0.009) and active LN (p=0.034).
- MPO-DNA complex levels correlated with proteinuria, hematuria, casts, leukocyturia, and SLEDAI-R in active LN.
Conclusions:
- 39% of SLE patients had elevated MPO-DNA complex levels.
- Elevated MPO-DNA complex is linked to a higher prevalence and activity of LN.
- MPO-DNA complex may serve as a potential biomarker for renal damage activity in SLE.
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