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Interleukin-35: A Serological Biomarker for Patients with Polymyositis/Dermatomyositis
Qinglai Jiang1, Yuxuan Li1, Liping Xia1
1Department of Rheumatology and Immunology, the First Affiliated Hospital of China Medical University, Shenyang, P.R. China.
Abstract:
Interleukin (IL)-35 is confirmed as an important modulator in immune response. The aim of the study was to explore the role of IL-35 in the development of polymyositis/dermatomyositis (PM/DM). Ninety-five patients with PM/DM and 30 healthy controls (HCs) were recruited. Peripheral blood mononuclear cells (PBMCs) were isolated by Ficoll-Paque Plus density gradient centrifugation. Protein IL-35, IL-17, and tumor necrosis factor (TNF)-α levels were measured using enzyme-linked immunosorbent assay method. The IL-35 serum levels in PM/DM patients were significantly higher than those in HCs and were correlated with PM/DM-related features: disease activity, muscle damage, and interstitial lung disease (ILD). Exogenous IL-35 notably suppressed lipopolysaccharide-induced IL-17 and TNF-α production in PBMCs of patients with PM/DM. Elevated serum IL-35 levels could act as a disease activity biomarker and an indicator of ILD in PM/DM. IL-35 may play an anti-inflammatory role in PM/DM.
Insights
Interleukin (IL)-35, a key immune modulator, is elevated in polymyositis/dermatomyositis (PM/DM) patients. Higher IL-35 levels correlate with disease activity and interstitial lung disease, suggesting an anti-inflammatory role.
Area of Science:
- Immunology
- Rheumatology
- Molecular Biology
Background:
- Interleukin (IL)-35 is recognized as a crucial regulator of immune responses.
- Polymyositis/dermatomyositis (PM/DM) are inflammatory myopathies with complex immune system involvement.
Purpose of the Study:
- To investigate the role and significance of IL-35 in the pathogenesis of polymyositis/dermatomyositis (PM/DM).
- To assess IL-35 serum levels in PM/DM patients compared to healthy controls and correlate findings with clinical features.
Main Methods:
- Recruitment of 95 PM/DM patients and 30 healthy controls (HCs).
- Isolation of peripheral blood mononuclear cells (PBMCs).
- Quantification of serum IL-35, IL-17, and tumor necrosis factor-alpha (TNF-α) using enzyme-linked immunosorbent assay (ELISA).
Main Results:
- PM/DM patients exhibited significantly higher serum IL-35 levels than HCs.
- Elevated IL-35 levels correlated with disease activity, muscle damage, and interstitial lung disease (ILD) in PM/DM.
- In vitro, IL-35 suppressed lipopolysaccharide-induced IL-17 and TNF-α production in PM/DM patient PBMCs.
Conclusions:
- Serum IL-35 may serve as a valuable biomarker for disease activity and an indicator of ILD in PM/DM.
- IL-35 appears to exert an anti-inflammatory effect within the context of PM/DM.
- Further research into IL-35's therapeutic potential in PM/DM is warranted.
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