Novel biomarkers for the assessment of paediatric systemic lupus erythematosus nephritis

Author:

Koutsonikoli A1,Trachana M1,Farmaki E1,Tzimouli V1,Pratsidou-Gertsi P1,Printza N1,Garyphallos A2,Galanopoulou V3,Kanakoudi-Tsakalidou F1,Papachristou F1

Affiliation:

1. 1st Department of Pediatrics, Aristotle University, ‘Hippokration’ General Hospital, Thessaloniki, Greece

2. 4th Department of Internal Medicine, Aristotle University, ‘Hippokration’ General Hospital, Thessaloniki, Greece

3. Department of Rheumatology, ‘Papageorgiou’ General Hospital, Thessaloniki, Greece

Abstract

Summary The discovery of serum biomarkers specific for paediatric lupus nephritis (pLN) will facilitate the non-invasive diagnosis, follow-up and more appropriate use of treatment. The aim of this study was to explore the role of serum high-mobility group box 1 (HMGB1) protein, antibodies against nucleosomes (anti-NCS), complement factor C1q (anti-C1q) and glomerular basement membrane (anti-GBM) in pLN. Serum samples of 42 patients with paediatric systemic lupus erythematosus (pSLE) (22 with pLN and 20 without renal involvement), 15 patients with other autoimmune nephritis (AN) and 26 healthy controls (HCs) were examined using enzyme-linked immunosorbent assay (ELISA). The activity of both pSLE and pLN was assessed by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) tool. The levels of all four biomarkers were significantly higher in pLN compared to AN and to HCs. The anti-NCS, anti-GBM and HMGB1 serum levels were significantly higher in pLN than in pSLE without renal involvement. The anti-C1q and the HMGB1 serum levels were correlated positively with pSLE activity. The HMGB1 serum levels were also correlated positively with pLN activity. These findings suggest that serum anti-NCS, anti-GBM and HMGB1 may serve as biomarkers specific for the presence of nephritis in pSLE. HMGB1 emerged as a useful biomarker for the assessment of pLN and pSLE activity, whereas anti-C1q only of pSLE activity.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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