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New biomarkers in IgA nephropathy.
Zhixin Xu1, Haoting Zhan1, Jingdi Zhang1
1Department of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Clinical Immunology (Orlando, Fla.)
|March 1, 2025
Summary
Immunoglobulin A nephropathy (IgAN) diagnosis needs better biomarkers beyond invasive kidney biopsies. Research is exploring new markers like microRNAs and metabolites for faster IgAN detection and prognosis.
Area of Science:
- Nephrology
- Immunology
- Biomarker Discovery
Background:
- Immunoglobulin A nephropathy (IgAN) is a leading cause of chronic kidney disease.
- Current diagnosis relies on invasive renal biopsies, limiting patient eligibility and accessibility.
- There is a critical need for non-invasive biomarkers for IgAN diagnosis and progression prediction.
Purpose of the Study:
- To review the current landscape of biomarkers for IgA nephropathy.
- To highlight the limitations of traditional diagnostic methods.
- To discuss emerging biomarkers for IgAN diagnosis, prognosis, and progression.
Main Methods:
- Literature review of IgAN diagnostic and prognostic markers.
- Analysis of traditional and novel biomarker categories.
- Discussion of galactose-deficient IgA1 (Gd-IgA1) and other emerging markers.
Main Results:
- Renal biopsy remains the gold standard but has significant limitations.
- Galactose-deficient IgA1 (Gd-IgA1) is a key target antibody.
- Emerging biomarkers include microRNAs, complement factors, proteases, inflammatory molecules, and metabolite profiles.
Conclusions:
- Non-invasive biomarkers are crucial for timely IgAN diagnosis and management.
- Advancements in biomarker research offer hope for improved patient outcomes.
- A multi-biomarker approach may enhance diagnostic accuracy and prognostic capabilities for IgAN.

