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Circulating CD14+HLA-DR-/low Myeloid-Derived Suppressor Cells as Potential Biomarkers for the Identification of
Shipeng Sun1, Yali Wei2, Xue Zeng2
1Clinical Laboratories, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Insights
Researchers identified potential biomarkers for Traditional Chinese Medicine (TCM) syndromes in psoriasis. Increased Mo-MDSCs and specific mRNA levels may help differentiate blood-heat and blood-stasis syndromes in psoriasis patients.
Area of Science:
- Immunology
- Dermatology
- Traditional Chinese Medicine (TCM)
Background:
- Psoriasis is a chronic autoimmune disease requiring better diagnostic tools.
- Traditional Chinese Medicine (TCM) classifies psoriasis into distinct syndromes, such as blood-heat (BH) and blood-stasis (BS).
- Identifying biomarkers for these TCM syndromes can aid in understanding disease heterogeneity and developing targeted therapies.
Purpose of the Study:
- To investigate circulating monocytic myeloid-derived suppressor cells (Mo-MDSCs) and associated immune factors in psoriasis patients.
- To identify potential biomarkers for differentiating between TCM blood-heat (BH) and blood-stasis (BS) syndromes in psoriasis.
Main Methods:
- Analysis of Mo-MDSC frequency (CD14+HLA-DR-/low cells within CD14+ cells) in peripheral blood.
- Quantification of serum immune factors (cytokines and enzymes).
- Measurement of mRNA expression levels of key immune genes in peripheral blood mononuclear cells (PBMCs).
Main Results:
- Mo-MDSC frequency was significantly higher in plaque psoriasis patients with blood-stasis (BS) syndrome compared to healthy controls and blood-heat (BH) syndrome patients.
- Serum levels of several cytokines (IL-2, IL-4, IL-6, IL-10, IL-17A, TNF-α, IFN-γ) and enzymes (iNOS, Arg-1) did not differ significantly between groups.
- Increased mRNA expression of Arg-1, TNF-α, ROR-γ, and PD-L1, and decreased mRNA expression of PD-1 and IL-10 were observed in PBMCs of psoriasis patients compared to controls.
- Distinct mRNA expression patterns for TNF-α and FOXP3 were found between the BH and BS syndrome groups.
Conclusions:
- The percentage of CD14+HLA-DR-/low Mo-MDSCs within CD14+ cells is a potential biomarker for distinguishing psoriasis TCM syndromes.
- Differential mRNA expression of TNF-α and FOXP3 in PBMCs may serve as biomarkers for differentiating between TCM BH and BS syndromes in psoriasis.
Abstract:
Psoriasis is a chronic autoimmune disease. Identification of the biomarkers responsible for Traditional Chinese Medicine (TCM) syndromes of psoriasis can help researchers recognize the different aspects of psoriasis and find novel therapeutic targets for the treatment of psoriasis. The current study investigated the levels of circulating Mo-MDSCs and Mo-MDSC-associated immune factors in the peripheral blood of psoriasis patients with different TCM syndromes. We found that the frequency of Mo-MDSCs (CD14+HLA-DR-/low cells) among CD14+ cells from plaque psoriasis patients with blood-stasis (BS) syndrome was significantly increased when compared with healthy controls (p < 0.001) and blood-heat (BH) syndrome group (p < 0.001), respectively. However, serum IL-2, IL-4, IL-6, IL-10, IL-17A, TNF-α, IFN-γ, iNOS, Arg-1, and NO concentration showed no statistically significant difference between healthy controls and psoriasis patients as well as no significant difference between the BH and BS syndrome groups. Compared with healthy controls, the mRNA expression of Arg-1, TNF-α, ROR-γ, and PD-L1 was increased, while the mRNA expression of PD-1 and IL-10 was decreased in PBMCs from psoriasis patients. Moreover, the mRNA expression of TNF-α and FOXP3 in PBMCs showed a pronounced statistical difference between the psoriatic BH syndrome group and the BS syndrome group. Therefore, we provide evidence that the percentage of CD14+HLA-DR-/low MDSC/ CD14+ cells and TNF-α and Foxp3 mRNA expression levels in PBMCs are potential biomarkers for distinguishing TCM BH syndrome and BS syndrome.
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