Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Mar 1:13:789713.
doi: 10.3389/fimmu.2022.789713. eCollection 2022.

Therapies for Membranous Nephropathy: A Tale From the Old and New Millennia

Affiliations
Review

Therapies for Membranous Nephropathy: A Tale From the Old and New Millennia

Francesco Scolari et al. Front Immunol. .

Abstract

Primary Membranous Nephropathy (PMN) is the most frequent cause of nephrotic syndrome in adults. If untreated, PMN can lead to end-stage renal disease; moreover, affected patients are at increased risk of complications typical of nephrotic syndrome such as fluid overload, deep vein thrombosis and infection. The association of PMN with HLA-DQA1 and the identification in around 70% of cases of circulating autoantibodies, mainly directed towards the phospholipase A2 receptor, supports the autoimmune nature of the disease. In patients not achieving spontaneous remission or in the ones with deteriorating kidney function and severe nephrotic syndrome, immunosuppression is required to increase the chances of achieving remission. The aim of this review is to discuss the evidence base for the different immunosuppressive regimens used for PMN in studies published so far; the manuscript also includes a section where the authors propose, based upon current evidence, their recommendations regarding immunosuppression in the disease, while highlighting the still significant knowledge gaps and uncertainties.

Keywords: cyclical therapy; glomerulonephitis; membranous nephropathy; nephrotic syndome; rituximab.

PubMed Disclaimer

Conflict of interest statement

FA declares consultancy fees from Baxter, AstraZeneca and Otsuka, advisory board for Trevere Therapeutics. These CIs are not relevant for the topic of the submitted paper. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

    1. Debiec H, Guigonis V, Mougenot B, Decobert F, Haymann J-P, Bensman A, et al. . Antenatal Membranous Glomerulonephritis Due to Anti–Neutral Endopeptidase Antibodies. N Engl J Med (2002) 346(26):2053–60. doi: 10.1056/NEJMoa012895 - DOI - PubMed
    1. Beck LH, Bonegio RGB, Lambeau G, Beck DM, Powell DW, Cummins TD, et al. . M-Type Phospholipase a 2 Receptor as Target Antigen in Idiopathic Membranous Nephropathy. N Engl J Med (2009) 361(1):11–21. doi: 10.1056/NEJMoa0810457 - DOI - PMC - PubMed
    1. Tomas NM, Beck LH, Meyer-Schwesinger C, Seitz-Polski B, Ma H, Zahner G, et al. . Thrombospondin Type-1 Domain-Containing 7A in Idiopathic Membranous Nephropathy. N Engl J Med (2014) 371(24):2277–87. doi: 10.1056/NEJMoa1409354 - DOI - PMC - PubMed
    1. Sethi S, Debiec H, Madden B, Vivarelli M, Charlesworth MC, Ravindran A, et al. . Semaphorin 3B–Associated Membranous Nephropathy Is a Distinct Type of Disease Predominantly Present in Pediatric Patients. Kidney Int (2020) 98(5):1253–64. doi: 10.1016/j.kint.2020.05.030 - DOI - PubMed
    1. Sethi S. New ‘Antigens’ in Membranous Nephropathy. J Am Soc Nephrol (2021) 32(2):268–78. doi: 10.1681/ASN.2020071082 - DOI - PMC - PubMed