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Published on: June 2, 2022
Treg/Th17 functional disequilibrium in Chinese uremia on hemodialysis: a link between calcification and
Danyan Chen1, Xiaolong Huang, Mengxue Yang
1Department of Nephrology, the First Affiliated Hospital of Chongqing Medical University, Chongqing, PR China. 13667623530@163.com
Insights
Functional disequilibrium in regulatory T cells (Treg)/T-helper (Th17) cells is linked to calcification and cardiovascular disease (CVD) outcomes in uremic patients undergoing hemodialysis (HD). This imbalance may synergistically contribute to the high incidence of CVD post-HD.
Area of Science:
- Immunology
- Nephrology
- Cardiovascular Medicine
Background:
- Uremic patients undergoing hemodialysis (HD) exhibit a high incidence of cardiovascular disease (CVD).
- The balance between regulatory T cells (Treg) and T-helper 17 (Th17) cells is crucial for immune homeostasis.
- Functional disequilibrium of Treg/Th17 cells is implicated in various inflammatory and autoimmune conditions.
Purpose of the Study:
- To investigate the correlation between Treg/Th17 cell functional disequilibrium and calcification in uremic patients.
- To explore the influence of Treg/Th17 cell imbalance on the outcome of CVD in patients on maintenance hemodialysis (MHD).
Main Methods:
- Compared Treg and Th17 cell frequencies, gene expressions (Foxp3, ROR-γt), and cytokine levels (IL-10, IL-17) in uremic patients with and without CVD, and healthy controls.
- Utilized flow cytometry, real-time quantitative polymerase chain reaction, and enzyme-linked immunosorbent assay.
- Investigated the effect of recombinant human bone morphogenetic protein-2 (rhBMP-2) on Treg/Th17 cells.
Main Results:
- rhBMP-2 upregulated Treg/Th17 functional disequilibrium in uremic patients, showing increased Treg and Th17 frequencies, gene expressions, and cytokine levels compared to controls.
- Significant differences in Treg/Th17 disequilibrium were observed between uremic patients with CVD (MHD group1) and those without CVD (MHD group2).
- Treg/Th17 functional disequilibrium correlated with calcification status and was consistent with the presence of CVD.
Conclusions:
- Treg/Th17 cell functional disequilibrium is associated with calcification in uremic patients.
- This immune cell imbalance may synergistically contribute to the high incidence of cardiovascular disease in patients undergoing hemodialysis.
Aim:
To investigate the correlation of the functional disequilibrium of regulatory T cells (Treg)/T-helper (Th17) cells with calcification and to explore the significance of their influence on the outcome of cardiovascular disease (CVD) in uremic patients after hemodialysis (HD).
Methods:
Out of 66 uremia patients, 36 patients had CVD after HD (maintenance hemodialysis (MHD) group1) and 30 patients did not have CVD (MHD group2). Twenty healthy volunteers were selected as normal control group. Peripheral blood mononuclear cells were isolated and treated with recombinant human bone morphogenetic protein-2 (rhBMP-2). Treg and Th17 frequencies were measured by flow cytometry. Forkhead/winged helix transcription factor (Foxp3) and retinoic acid receptor-related orphan receptor-γt (ROR-γt) mRNA expressions were measured by real-time quantitative polymerase chain reaction. Levels of interleukin (IL)-10 and IL-17 were detected by enzyme-linked immunosorbent assay.
Results:
When compared with controls, rhBMP-2 upregulates Treg/Th17 functional disequilibrium in uremia patients, displaying higher Treg and Th17 frequencies, Foxp3 and ROR-γt expressions, and levels of cytokines (p < 0.05). These differences were also significant between MHD group1 and group2 (p < 0.05). It was also observed that Treg/Th17 functional disequilibrium was not only correlated with a calcification state but also consistent with the CVD.
Conclusion:
The Treg/Th17 cell function disequilibrium might act synergistically with calcification in the high incidence of CVD after HD.
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