Evidence map›Paper›PMID 39099913›Full record

ArticleCureus2024

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

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

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Elevated IL-10 is Linked With the Expansion of T-betJournal of clinical immunology · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shradha VermaBiochemistry, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Seema ShahBiochemistry, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Rachita NandaBiochemistry, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Jhasaketan MeherGeneral Medicine, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Vinay RathoreNephrology, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Suprava PatelBiochemistry, All India Institute of Medical Sciences, Raipur, Raipur, IND.
Eli MohapatraBiochemistry, All India Institute of Medical Sciences, Raipur, Raipur, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSystemic 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

methodsThis 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.

conclusionIn 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.

Indexed as

correlationinterleukin-10lupus nephritissystemic lupus erythematosusth10 cells

Identifiers

PMID39099913
PMCPMC11298017

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