IgA Nephropathy: Emerging Mechanisms of Disease

Author:

Roberts Lydia E.12,Williams Chloe E.C.34,Oni Louise45,Barratt Jonathan12,Selvaskandan Haresh12

Affiliation:

1. John Walls Renal Unit, University Hospitals of Leicester NHS Trust and University of Leicester, Leicester, United Kingdom

2. Department of Cardiovascular Sciences, University of Leicester, Leicester, United Kingdom

3. Royal Liverpool and Broadgreen University Hospital Trusts, Liverpool, United Kingdom

4. Department of Women’s and Children’s Health, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, United Kingdom

5. Department of Paediatric Nephrology, Alder Hey Children’s NHS Foundation Trust Hospital, Liverpool, United Kingdom

Abstract

Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis reported across the world and is characterized by immunoglobulin A (IgA) dominant mesangial deposits, which are poorly O-glycosylated. This deposition leads to a cascade of glomerular and tubulointerstitial inflammation and fibrosis, which can progress to chronic kidney disease. The variability in rate of progression reflects the many genetic and environmental factors that drive IgAN. Here, we summarize the contemporary understanding of the disease mechanisms that drive IgAN and provide an overview of new and emerging therapies, which target these mechanisms.

Publisher

Scientific Scholar

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