Evidence map›Paper›PMID 42394403›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

The Synthetic Melanocortin Agonist NDP-MSH Ameliorates THSD7A-Associated Membranous Nephropathy in an Active Immunization Mouse Model.

Mingzhuo Zhang, Mengxuan Chen, Yan Ge, William Gunning, Rujun Gong

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Mingzhuo ZhangDivision of Nephrology, Department of Medicine, University of Toledo College of Medicine, Toledo, Ohio, USA.ORCID https://orcid.org/0000-0003-0088-1138
Mengxuan ChenDivision of Nephrology, Department of Medicine, University of Toledo College of Medicine, Toledo, Ohio, USA.
Yan GeDivision of Nephrology, Department of Medicine, University of Toledo College of Medicine, Toledo, Ohio, USA.
William GunningDepartment of Pathology, University of Toledo College of Medicine, Toledo, Ohio, USA.
Rujun GongDivision of Nephrology, Department of Medicine, University of Toledo College of Medicine, Toledo, Ohio, USA.ORCID https://orcid.org/0000-0002-6302-2800

Funding

HHS | National Institutes of Health (NIH) DK114006HHS | National Institutes of Health (NIH) DK133203
6 · The paper itself

Abstract

Melanocortin-based therapies have demonstrated protective effects in experimental membranous nephropathy (MN). However, existing evidence is derived exclusively from passive immunization models that lack direct involvement of human MN-associated autoimmunity, limiting translational relevance. A clinically relevant model is essential to more precisely define melanocortin efficacy and mechanisms in MN. To address this gap, we established an active immunization model of THSD7A-associated MN by immunizing mice with recombinant THSD7A antigen. This clinically relevant and accessible model recapitulated cardinal features of human MN, including insidious onset, progressive proteinuria, and characteristic histopathology such as subepithelial immune deposition, complement fixation along glomerular tufts, glomerular basement membrane thickening, and podocyte injury with foot process effacement and loss of homeostatic markers. Rescue treatment with the pan-melanocortin receptor agonist NDP-MSH significantly reduced proteinuria and mitigated glomerular damage and podocyte injury. This was accompanied by a marked reduction in circulating anti-THSD7A autoantibody levels, reduced glomerular immune deposition, and diminished complement activation. Mechanistically, ex vivo treatment of primed B cells isolated from diseased mice demonstrated that NDP-MSH directly inhibited plasma cell differentiation and autoantibody production. This suppression was accompanied by increased expression of microphthalmia-associated transcription factor (MITF) and downregulation of interferon regulatory factor 4 (IRF4), indicating activation of the MITF/IRF4 signaling axis, a pathway implicated in negative regulation of B cell differentiation. Collectively, these findings extend the therapeutic potential of melanocortin signaling to a preclinical model that closely mirrors human MN and provide mechanistic insight into its immunomodulatory actions. These results support further investigation of targeted melanocortin-based therapies for MN.

Indexed as

alpha-MSHGlomerulonephritis, MembranousMelanocortinsAnimalsDisease Models, AnimalHumansImmunizationMiceMice, Inbred C57BLPodocytesProteinuriaReceptors, Melanocortinalpha-MSHMelanocortinsMSH, 4-Nle-7-Phe-alpha-Receptors, Melanocortinalbuminuriaglomerular diseasemelanocortinmembranous nephropathyplamsa cells

Identifiers

PMID42394403
PMCPMC13329422

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.