Abstract: TH-PO0675
Immune Cell Characteristics in a Gut-Kidney Axis-Induced Mouse Model of IgAN
Session Information
- Glomerular Diseases: Immunopathogenesis and Targeted Therapeutics
November 06, 2025 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Glomerular Diseases
- 1401 Glomerular Diseases: Mechanisms, including Podocyte Biology
Authors
- Liu, Jiaqi, Shenzhen Second People's Hospital, Shenzhen, Guangdong, China
- Chen, Yuna, Shenzhen Second People's Hospital, Shenzhen, Guangdong, China
- Wan, Qijun, Shenzhen Second People's Hospital, Shenzhen, Guangdong, China
Background
IgA nephropathy(IgAN) is the leading type of primary glomerulonephritis, significantly contributing to chronic kidney disease(CKD) and renal failure.The pathogenesis of IgAN is the multi-hit hypothesis regarding overproduction and accumulation of galactose-deficient(Gd-IgA1).Recent findings have revealed gut microbiota dysbiosis and immune responses are essential in the development of IgAN, attracting increasing attention.This study aimed to map mucosal immune cells in IgAN influenced by gut microbiota, investigating the role of innate immune cells in kidney damage.
Methods
Fecal samples were acquired from both patients and controls for subsequent animal experiments.Mice received a broad-spectrum antibiotic cocktail to eliminate their intestinal microflora,followed by a gavage with fecal microbiota from clinical individuals.Murine intestinal and kidney tissues were collected for flow cytometry.Intestine and kidney histopathology,immunofluorescence,and inflammatory cytokine expression were assessed in the murine models.The mucosal epithelium's structure and function,along with the innate immune cell response,were analyzed.
Results
Mice exhibited the IgAN phenotype following colonization with gut microbiota from IgAN patients. These mice(IgAN-FMT mice) showed renal dysfunction and increased pathology of tissue injury in both intestine and kidneys. IgAN-FMT mice showed heightened pro-inflammatory cytokine activity, greater antibody (IgA and complement C3) deposition and decreased expression of mucosal barrier protein(ZO-1, Occludin) compared to the control group.Innate immune cells profile in the murine intestine and kidneys were mapped. Especially, CD11c+dendritic cells were more abundant compared to the control group.
Conclusion
The gut-kidney axis, including microbiota homeostasis and innate immune cell response, contributes to the pathogenesis of IgAN. Gut dysbiosis and hyperactivated immune cells like CD11c+dendritic cells can affect the mucosal barrier and exacerbate the renal damage, being novel insights into immunotherapeutic strategies for IgAN.
Funding
- NIDDK Support