# Exploring the Role of Th10 Cells and IL-10 in Systemic Lupus Erythematosus

**Authors:** Shradha Verma, Seema Shah, Rachita Nanda, Jhasaketan Meher, Vinay Rathore, Suprava Patel, Eli Mohapatra

PMC · DOI: 10.7759/cureus.63875 · Cureus · 2024-07-05

## TL;DR

This study explores how Th10 cells and IL-10 are linked to disease activity in systemic lupus erythematosus (SLE), suggesting they could be useful biomarkers for monitoring the condition.

## Contribution

The study identifies Th10 cells and IL-10 as potential biomarkers for SLE disease activity, particularly in relation to nephritis.

## Key findings

- Th10 cells and IL-10 levels are significantly higher in SLE patients compared to healthy controls.
- Th10 cells and IL-10 correlate positively with SLE disease activity scores (SLEDAI).
- Th10 cell expression is significantly elevated in SLE patients with nephritis.

## Abstract

Introduction: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibody production and immune complex deposition in various organs. The pathogenesis of SLE is multifactorial, involving genetic, hormonal, environmental, and immune factors. Interleukin-10 (IL-10) is a pleiotropic cytokine produced by various immune cells and has conflicting roles in inflammation.

Materials and methods: This is a cross-sectional study involving 56 SLE patients and 30 healthy controls.

Results and analysis: We found a significant increase in T helper 10 (Th10) cells and IL-10 levels in SLE patients compared to controls. Disease activity, measured by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score, correlated positively with Th10 cells and IL-10 levels. Further analysis categorized patients into active and inactive SLE, showing significant differences in laboratory parameters, including C3, C4, Th10 cells, and IL-10, between the two groups. Notably, Th10 cells and IL-10 exhibited a significant positive correlation with SLEDAI scores. The study also explored SLE patients with and without nephritis, a severe manifestation of the disease. Th10 cell expression was significantly higher in nephritis patients, while IL-10 levels did not differ significantly between the two groups.

Conclusion: In conclusion, this study provides valuable insights into the association between Th10 cells, IL-10, and disease activity in SLE. The findings suggest that Th10 cells and IL-10 could serve as potential biomarkers for disease activity in SLE, offering a basis for further research into therapeutic interventions targeting these factors. These results contribute to our understanding of the complex immunological factors at play in SLE and may pave the way for more targeted and effective treatment approaches.

## Linked entities

- **Proteins:** IL10 (interleukin 10)
- **Diseases:** Systemic lupus erythematosus (MONDO:0007915), nephritis (MONDO:0001166)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** SLE (MESH:D008180), inflammation (MESH:D007249), nephritis (MESH:D009393), autoimmune disease (MESH:D001327)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC11298017/full.md

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Source: https://tomesphere.com/paper/PMC11298017