# Serum IL-2 levels are associated with disease activity and related to dyslipidaemia and the immunological profile in systemic lupus erythematosus

**Authors:** Miguel Ángel Gonzalez-Gay, Fuensanta Gómez-Bernal, Beatriz Tejera-Segura, Juan Carlos Quevedo-Abeledo, Enrique García-Barrera, Luisa María Villar, J Gonzalo Ocejo-Vinyals, Raquel Largo, Iván Ferraz-Amaro

PMC · DOI: 10.1136/lupus-2025-001870 · 2026-03-12

## TL;DR

This study finds that IL-2 levels in lupus patients are linked to disease activity, inflammation, and lipid levels, suggesting a key role in lupus progression.

## Contribution

The study establishes novel associations between serum IL-2 and specific autoantibodies, inflammation markers, and dyslipidaemia in SLE patients.

## Key findings

- Serum IL-2 levels are positively associated with inflammatory markers like CRP and IL-6 in SLE patients.
- Higher IL-2 levels correlate with disease activity and specific autoantibodies such as anti-DNA and anti-SSA/SSB.
- Triglycerides are positively linked to IL-2, while HDL-cholesterol is inversely associated.

## Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disorder characterised by multisystem involvement, frequently including cardiovascular manifestations. Interleukin 2 (IL-2), a key cytokine in immune regulation, plays a pivotal role in maintaining tolerance by promoting regulatory T cell function. The relationship between serum IL-2 levels and specific SLE features remains incompletely defined. The aim of our study was to investigate the associations between serum IL-2 concentrations and disease activity, inflammatory markers, autoantibody profiles as well as cardiovascular and metabolic parameters in a well-characterised cohort of patients with SLE.

In this cross-sectional study, 235 patients with SLE were recruited and characterised, including assessment of autoantibody profiles, disease activity indices (SLE Disease Activity Index-2000 (SLEDAI-2K)), Damage Index and remission status. Cardiovascular characteristics were evaluated, encompassing lipid profiles, insulin resistance indices and carotid ultrasound parameters such as plaque presence, intima-media thickness and arterial stiffness. Serum IL-2 concentrations were quantified using an ultrasensitive technique, the Single Molecule Array (Simoa). Multivariable linear regression was conducted to examine the associations between circulating IL-2 levels and clinical as well as cardiovascular manifestations of SLE.

In multivariable analyses, serum IL-2 levels showed significant positive associations with inflammatory markers including C reactive protein and IL-6. Disease activity, assessed by SLEDAI-2K, was positively correlated with IL-2 levels. Positive and significant associations were also noted, after adjustment for covariates, between IL-2 and specific autoantibodies, including anti-DNA, anti-Sjögren’s syndrome antigen A (SSA), anti-Sjögren’s syndrome antigen B (SSB), anti-Smith (Sm) and antiribosome. Regarding cardiovascular disease factors, triglycerides were positively associated with IL-2 whereas high-density lipoprotein-cholesterol exhibited an inverse relationship.

Significant correlations exist between serum IL-2 levels and markers of inflammation, lipid profile, disease activity and specific autoantibody profiles in patients with SLE. These findings underscore the pivotal role of IL-2 in SLE immunopathogenesis, reflecting its intricate involvement in modulating both inflammatory responses and metabolic pathways.

## Linked entities

- **Proteins:** IL2 (interleukin 2), IL6 (interleukin 6)
- **Diseases:** systemic lupus erythematosus (MONDO:0007915), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TRIM21 (tripartite motif containing 21) [NCBI Gene 6737] {aka RNF81, RO52, Ro/SSA, SSA, SSA1, TRIM21/Ro52}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, SSB (small RNA binding exonuclease protection factor La) [NCBI Gene 6741] {aka LARP3, La, La/SSB, SSB/La}
- **Diseases:** inflammation (MESH:D007249), autoimmune disorder (MESH:D001327), SLE (MESH:D008180), cardiovascular disease (MESH:D002318), insulin resistance (MESH:D007333)
- **Chemicals:** triglycerides (MESH:D014280), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12983779/full.md

---
Source: https://tomesphere.com/paper/PMC12983779