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Updated: Aug 11, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Lupus Membranous Nephropathy
Claudio Ponticelli1, Gabriella Moroni2, Alessia Fornoni3
1Nephrology, IRCCS Ospedale Maggiore Policlinico (retired), Milan, Italy.
Background:
Lupus membranous nephropathy (LMN) is a rare disease, usually associated with nephrotic syndrome.
Methods:
We reviewed the literature by searching for the following terms on Pubmed.gov: lupus nephritis, membranous nephropathy (MN), lupus membranous nephropathy, nephrotic syndrome, and Class V lupus nephritis.
Results:
The histology of LMN at light microscopy is similar to that of primary MN. Cases of MN associated with focal or diffuse proliferation are not considered LMN by the International Society of Nephrology/Renal Pathology Society classification. Immunofluorescence study of LMN shows deposits of all immunoglobulins and complement. Tubulo-reticular structures, extraglomerular deposits, subepithelial, and scanty subendothelial deposits can be seen on electron microscopy. Phospholipase A2 receptor deposits are usually but not necessarily absent in LMN. The pathogenesis is still not completely understood. The inflammatory milieu of lupus may favor the development of autoantigens and intraglomerular assembly of immune complexes. These are more often associated with mesangial or endocapillary hypercellular lesions. Alternatively, autoantibodies may bind autoantigens in the glomerular subepithelium, triggering a signaling cascade leading to LMN. A central role in the development of podocyte injury and proteinuria is played by the components of complement C5b-C9. CKD progression in LMN is slow but may be accelerated by the frequency of renal flares. Persistent nephrotic syndrome and/or the frequent use of corticosteroids may lead to a series of life-threatening complications.
Discussion:
Treatment of arterial hypertension, dyslipidemia, and diabetes are of paramount importance. Besides specific therapies of these complications, hydroxychloroquine and vitamin D supplementation are recommended. Immunosuppression should be limited to patients with nephrotic proteinuria. The most frequently used drugs are corticosteroids, calcineurin inhibitors, cyclophosphamide, mycophenolate, and rituximab, alone or combined. Early detection and treatment of renal flares is of paramount importance to prevent CKD progression.
Insights
Lupus membranous nephropathy (LMN) is a rare kidney disease often causing nephrotic syndrome. Early detection and treatment are crucial to prevent chronic kidney disease progression and complications.
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- Lupus membranous nephropathy (LMN) is a rare autoimmune kidney disease.
- It is frequently associated with nephrotic syndrome, characterized by significant proteinuria.
Purpose of the Study:
- To review the literature on lupus membranous nephropathy (LMN).
- To understand the histology, pathogenesis, and treatment of LMN.
Main Methods:
- Literature search on PubMed using terms: lupus nephritis, membranous nephropathy (MN), LMN, nephrotic syndrome, Class V lupus nephritis.
- Review of histological findings (light, immunofluorescence, electron microscopy) and pathogenetic mechanisms.
Main Results:
- LMN histology resembles primary MN; specific classifications exclude proliferative lesions.
- Immunofluorescence shows immunoglobulin and complement deposits; electron microscopy reveals subepithelial deposits and tubulo-reticular structures.
- Pathogenesis involves lupus inflammation, autoantigens, immune complex assembly, and complement C5b-C9 activation, leading to podocyte injury and proteinuria.
Conclusions:
- Management includes controlling hypertension, dyslipidemia, and diabetes.
- Hydroxychloroquine and vitamin D are recommended; immunosuppression is reserved for nephrotic proteinuria.
- Early detection and treatment of renal flares are vital to prevent chronic kidney disease (CKD) progression.
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