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TREM-1 Contributes to Inflammation in IgA Nephropathy
Yan-Feng Zhao1,2,3,4, Li Zhu1,2,3,4, Li-Jun Liu1,2,3,4
1Renal Division, Department of Medicine, Peking University First Hospital, Beijing, China.
Circulating IgA1 immune complexes (cIgA1) drive kidney inflammation in IgA nephropathy (IgAN). Triggering receptor expressed on myeloid cells-1 (TREM-1) amplifies this inflammation, contributing to kidney injury in IgAN patients.
Area of Science:
- Nephrology
- Immunology
- Inflammation Research
Background:
- Circulating IgA1 immune complexes (cIgA1) are implicated in IgA nephropathy (IgAN) pathogenesis.
- cIgA1 can trigger inflammatory factors like MCP-1 and IL-6, contributing to kidney injury.
- Soluble TREM-1 (sTREM-1) was previously identified as upregulated by mesangial cells under cIgA1 challenge.
Purpose of the Study:
- To investigate the role of TREM-1 in cIgA1-induced kidney injury in IgAN.
- To explore the relationship between TREM-1, inflammation, and disease severity in IgAN patients.
Main Methods:
- Enrolled 35 IgAN patients and 17 healthy controls.
- Isolated cIgA1 and treated cultured mesangial cells.
- Measured TREM-1 mRNA, sTREM-1, MCP-1, and IL-6 levels in cell supernatant and urine.
Main Results:
- cIgA1 significantly upregulated TREM-1 expression in mesangial cells.
- sTREM-1 levels correlated positively with MCP-1 in mesangial cell supernatant.
- Higher urinary sTREM-1 levels were found in IgAN patients and associated with severe clinical and pathological manifestations.
Conclusions:
- TREM-1 plays a role in cIgA1-induced inflammatory kidney injury in IgAN.
- Urinary sTREM-1 may serve as a biomarker for disease severity in IgAN.
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