Evidence map›Paper›PMID 41531324›Full record

ArticleJournal of pathology and translational medicine2026

Significance of KM55 immunohistochemical staining in the diagnosis and prognosis of IgA nephropathy.

Hoe In Jeong, Beom Jin Lim, Minsun Jung

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Article in Journal of pathology and translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Hoe In JeongDepartments of Pathology, Yonsei University College of Medicine, Seoul, Korea.
Beom Jin LimDepartments of Pathology, Yonsei University College of Medicine, Seoul, Korea.
Minsun JungDepartments of Pathology, Yonsei University College of Medicine, Seoul, Korea.

Funding

The Korean Society of Pathologist KSPG2023-01
6 · The paper itself

Abstract

backgroundGalactose-deficient IgA1 (Gd-IgA1) plays a crucial role in IgA nephropathy (IgAN). The monoclonal antibody KM55 has emerged as a simplified method for detecting Gd-IgA1; however, the clinicopathological significance of immunohistochemistry for Gd-IgA1 remains underexplored. This study evaluated the prognostic and clinicopathological significance of KM55 immunohistochemistry in IgAN.

methodsA total of 114 native kidney biopsies showing at least mild mesangial IgA positivity on immunofluorescence were retrospectively analyzed. Patients were categorized as having IgAN or non-IgAN diseases. The KM55 immunohistochemical staining was graded as 0, 1+, 2+, 3, or 4+. Data on Oxford classification, laboratory parameters, and renal outcomes were collected.

resultsThe IgAN group showed significantly higher KM55 scores than the non-IgAN group (median: 3 vs. 1; p < .001). IgAN cases were further stratified into KM55-high (≥3+, n = 38) and -low groups (≤2+, n = 37). The KM55-high group had significantly higher diastolic blood pressure, blood urea nitrogen, creatinine, urine protein/creatinine ratio, and Oxford mesangial hypercellularity scores, along with lower estimated glomerular filtration rate (eGFR) and serum albumin. Cox analysis revealed significantly poorer outcomes in the KM55-high group for chronic kidney disease stage 4 (p = .015), end-stage renal disease (p = .024), and 75% eGFR decline (p = .016).

conclusionsMesangial Gd-IgA1 deposition graded by KM55 immunohistochemistry may be a useful adjunct for IgAN diagnosis and a potential prognostic biomarker.

Indexed as

Galactosyl-deficient IgA1Glomerulonephritis, IGAImmunohistochemistry

Identifiers

PMID41531324
PMCPMC13586529

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