Evidence map›Paper›PMID 40331437›Full record

ArticleACR open rheumatology2025

Urinary V-Set Ig Domain-Containing Protein 4 and Immune Complexes for Tracking Lupus Nephritis and Renal Pathology.

Aygun Teymur, Chenling Tang, Fariz Nazir, Neda Ostadnejad, Qi Cai, Ramesh Saxena, Tianfu Wu

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Aygun TeymurUniversity of Houston, Houston, Texas.ORCID https://orcid.org/0009-0005-1206-433X
Chenling TangUniversity of Houston, Houston, Texas.
Fariz NazirUniversity of Houston, Houston, Texas.
Neda OstadnejadUniversity of Houston, Houston, Texas.
Qi CaiUniversity of Texas Southwestern Medical Center, Dallas.
Ramesh SaxenaUniversity of Texas Southwestern Medical Center, Dallas.
Tianfu WuUniversity of Houston, Houston, Texas.ORCID https://orcid.org/0000-0003-4406-1449

Funding

A biomarker panel based smart mini-array system for the homecare of autoimmune kidney diseasesR01AG062987 · NIA · UNIVERSITY OF HOUSTON · PI WU, TIANFU · 2019 to 2023
$2.2M
NIA NIH HHS R01 AG062987NIH HHS AG062987
6 · The paper itself

Abstract

objectiveThis study aims to investigate whether V-set Ig domain-containing protein 4 (VSIG4; also known as complement receptor of the Ig superfamily [CRIg]) forms immune complexes (ICxs) with IgG and complement component 3 (C3) in the kidneys of patients with lupus nephritis (LN) and to assess the potential of urinary VSIG4 and VSIG4-ICx as noninvasive biomarkers of LN.

methodsImmunofluorescent staining was employed to detect the deposition of VSIG4 (CRIg), IgG, and C3 in kidney tissue. Urine samples from 102 patients with LN, 51 healthy controls (HCs), and 13 patients with chronic kidney disease (CKD) were analyzed via enzyme-linked immunosorbent assay for VSIG4-ICx and free-form VSIG4.

resultsImmunofluorescence costaining demonstrated the colocalization of VSIG4, IgG, and C3 in the kidneys of those with LN and elevated VSIG4 protein expression in the glomeruli regions in LN. Compared with HCs and those with CKD, patients with LN exhibited significantly elevated levels of urinary VSIG4 in both free form and ICx. Urinary VSIG4-ICx correlated with clinical parameters, including the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) (R = 0.55, P < 0.0001), renal SLEDAI (R = 0.52, P < 0.0001), estimated glomerular filtration rate (-0.5, P < 0.001), activity index (R = 0.25, P < 0.05), chronicity index (R = 0.32, P < 0.05), complement C3 (R = -0.33, P < 0.05), and complement C4 (R = -0.31, P < 0.05). The strong association of the urinary VSIG4-ICx with disease activity metrics and histopathologic evidence underscores its potential for clinical utility in diagnosing and monitoring LN.

conclusionVSIG4-ICx shows promise as a novel urine biomarker for LN, with potential utility for diagnosis and disease monitoring.

Identifiers

PMID40331437
PMCPMC12056603

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