| Background: Alongside many complications in understanding the etiology of Preeclampsia (PE), several determinants, such as the imbalanced proportion of anti-angiogenic/proangiogenic T-cell subsets, especially CD4+
(Th17/Treg), as well as alterations in the expression profle of related cytokines, miRNAs, and transcription
factors might have been implicated in PE pathogenesis.
Material and method: After sample collection and preparation, CD4+ cells were isolated from PE and non-PE
pregnant woman and were cultured. Furthermore, analysis such as flow cytometry, real-time PCR, western
blotting, and ELISA were performed to assess determinants related to PE manifestation, including sFlt-1, sEng,
STAT-3, RORγt, SMAD-7, Foxp3, IL-17, IL-22, Ets-1, and miRNA-326.
Results: Our results showed that the miRNA-326 expression level increased in CD4+ Cells and Th17 in PE patients
which downregulated Ets-1 expression that acts as a negative control for Th17 development. Furthermore, we
showed that the number and expression level of Th17 s and transcription factor RORγt escalated, respectively.
While Treg and its related transcription factor (Foxp3) demonstrated a decrease. Flow cytometry analysis
illustrated that the Th17/Treg ratio increased in PE. Additionally, we demonstrated that expression and concentration levels of cytokines (IL-17 and IL22) and anti-angiogenic molecules (sEng and sFlt-1) soared in isolated
CD4+ cells from PE patients, which could be correlated with PE pathogenicity.
Conclusion: In conclusion, we comprehensively evaluated immunological factors and molecules involved in PE
manifestation. Interestingly, the CD4+ T-cell subset could be an extra source of antiangiogenic factors for the
maintenance of this hypertension disorder. |