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Serum interferon-γ and urinary monocyte chemoattractant peptide-1 are important factors in the pathogenesis of IgA nephropathySerum interferon-γ and urinary monocyte chemoattractant peptide-1 are important factors in the pathogenesis of IgA nephropathy

Other Titles
Serum interferon-γ and urinary monocyte chemoattractant peptide-1 are important factors in the pathogenesis of IgA nephropathy
Authors
Han Sang YoubJeong Kyung HwanIhm Chun GyooKang Young Sun차대룡
Issue Date
3월-2021
Publisher
대한신장학회
Keywords
Chemokine CCL2; IGA glomerulonephritis; Interferons; T helper 1 cells; T helper 2 cells
Citation
Kidney Research and Clinical Practice, v.40, no.1, pp.69 - 76
Indexed
SCIE
SCOPUS
KCI
Journal Title
Kidney Research and Clinical Practice
Volume
40
Number
1
Start Page
69
End Page
76
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/129163
DOI
10.23876/j.krcp.20.157
ISSN
2211-9132
Abstract
Background: Imbalance of T helper (Th) 1/2 cells has been shown to contribute to the development of immunoglobulin A nephropa thy (IgAN). To address the inconsistent results on the role of Th1/Th2 polarization, we evaluated the levels of Th1/Th2 cytokines in various samples from patients with IgAN. Methods: Thirty-one patients with biopsy-proven IgAN (age, 34.48 ± 12.10 years) and 25 healthy controls (age, 44.84 ± 13.72 years) were enrolled. We evaluated the relationship between the levels of Th1/Th2 cytokines and the response to glucocorticoid treatment. Results: The levels of serum interferon-gamma (IFNγ) and urinary monocyte chemoattractant peptide (MCP)-1 were higher in the IgAN group than in the control group. The levels of MCP-1 in urine and secreted by peripheral blood mononuclear cells (PBMCs) were significantly different among three groups categorized based on daily proteinuria. The level of urinary MCP-1 was significantly cor related with proteinuria. The levels of urinary MCP-1, serum interleukin (IL)-4, IFNγ, and IL-2 secreted by PBMCs and intrarenal IL-1 messenger RNA (mRNA) were significantly correlated with the ratio of proteinuria at 6 months to baseline proteinuria in patients un dergoing glucocorticoid treatment. MCP-1 mRNA and protein levels were significantly upregulated in mesangial cells stimulated with IFNγ among representative Th1/Th2 cytokines. Conclusion: IFNγ was shown to be a key cytokine in the pathogenic processes underlying IgAN, and its upregulation induced an in crease in urinary MCP-1 production. These findings suggest that Th1 cytokines may play an important role in the development of IgAN.
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