Evidence map›Paper›PMID 42865689›Full record

ArticleFrontiers in immunology2026

Eculizumab in rapidly progressive glomerulonephritis: a case-series report.

Xueting Li, Yinghui Zhang, Ben Ke

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. 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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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

3 authors.

Xueting LiDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Yinghui ZhangDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Ben KeDepartment of Nephrology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To describe the clinical outcomes and safety profile of eculizumab as adjunctive therapy in a case series of patients with rapidly progressive glomerulonephritis (RPGN) due to anti-glomerular basement membrane (GBM) disease and anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV). Methods: We reported 7 patients with AAV and 5 patients with anti-GBM disease who presented to our center between March 2025 and January 2026. All patients received eculizumab (900 mg, 1-4 doses) in addition to standard immunosuppressive therapy. Serum creatinine (Scr), urinary red blood cell (uRBC) count, urine protein-to-creatinine ratio (UPCR), and dialysis dependence were assessed at baseline and at 3 months. Adverse events were monitored throughout follow-up. Results: In AAV patients, mean Scr decreased from 407.38 μmol/L to 231.27 μmol/L ( Conclusion: In this descriptive case series, we observed trends toward improved renal function and hematuria at 3 months in patients with severe RPGN who received eculizumab in addition to standard immunosuppression, with earlier initiation and milder baseline renal impairment appearing to correlate with more favorable outcomes. Nevertheless, the lack of a control group and the marked interpatient variability in baseline characteristics and concomitant therapies preclude any conclusion regarding a causal effect of eculizumab. Instead, these data serve as real-world observations that can generate hypotheses for future studies. Definitive evidence on the efficacy and safety of eculizumab in RPGN must await larger, prospective, controlled investigations.

Indexed as

Antibodies, Monoclonal, HumanizedAnti-Glomerular Basement Membrane DiseaseAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisGlomerulonephritisAdultAgedDisease ProgressionFemaleHumansImmunosuppressive AgentsMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizedeculizumabImmunosuppressive Agentsanti-glomerular basement membrane diseaseanti-neutrophil cytoplasmic antibody-associated vasculitiscase serieseculizumabrapidly progressive glomerulonephritis

Identifiers

PMID42865689
PMCPMC13655034

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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 OpenQuestion graph.