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Th1/Th2 associated transcription factors and cytokines in pregnancies with systemic lupus erythematosus


1, 2, 3, 4, 5, 6

 

  1. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China.
  2. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China.
  3. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China.
  4. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China.
  5. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China.
  6. Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao China. wangjibo2005@126.com

CER17815
2025 Vol.43, N°1
PI 0105, PF 0111
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PMID: 39360363 [PubMed]

Received: 03/05/2024
Accepted : 01/08/2024
In Press: 17/09/2024
Published: 23/01/2025

Abstract

OBJECTIVES:
Th1/Th2 shift occurs during pregnancy. Systemic lupus erythematosus (SLE) flares may induce the dysregulation of Th1 and Th2 cells. We aimed to investigate the dynamic changes of Th1/Th2 associated transcription factors and cytokines in patients with SLE during pregnancy.
METHODS:
Twenty-five pregnant patients with SLE and twenty-two healthy age-matched women served as controls from September 2021 to March 2022 were enrolled in the study. Real-time quantitative reverse transcription polymerase chain reaction analysis of peripheral blood mononuclear cells were performed to measure the expression of Th1 specific transcription factors T-bet, cytokine IFN-γ, and Th2 specific transcription factors GATA3, cytokine IL-4. The main statistical analysis methods were t test, Mann-Whitney U-test, Pearson correlation and Spearman rank correlation analysis.
RESULTS:
The mRNA level of IFN-γ and the relative expression of T-bet/GATA3 and IFN-γ/IL-4 in SLE patients were significantly higher than those in healthy individuals, whereas the GATA3 expression is lower in pregnant patients with SLE (p<0.001, p<0.05, p<0.05 and p<0.01 during the whole pregnancy, respectively; p<0.05, p<0.01, p<0.05 and p<0.05 specifically for the 3rd trimester, respectively). There were significant correlations between T-bet and IFN-γ (r=0.492, p<0.05), and between T-bet/GATA3 and IFN-γ/IL-4 (r=0.482, p<0.05).
CONCLUSIONS:
Our work indicates that in SLE patients Th1/Th2 shift is blocked with up-regulation of Th1 cell function and insufficient Th2 polarisation during pregnancy, which may be involved in adverse pregnancy outcomes.

DOI: https://doi.org/10.55563/clinexprheumatol/rmp2pl

Rheumatology Article