Evidence map›Paper›PMID 40453547›Full record

ArticleJournal of translational autoimmunity2025

Immune characterization of lupus nephritis patients undergoing dialysis.

Quentin Simon, François Gaillard, John Tchen, Delphine Bachelet, Karim Sacré, Katell Peoc'h, Noémie Jourde-Chiche, Eric Daugas, Nicolas Charles

Registry-linked trialAbstract read
In one paragraph

Article in Journal of translational autoimmunity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03921398 (Identifying New Therapeutic Targets for Lupus Treatment), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT03921398 completednot on this map

Identifying New Therapeutic Targets for Lupus Treatment

Typeobservational_patient_registrySponsorAssistance Publique - Hôpitaux de ParisRan2019 to 2022Enrolled87ConditionsLupus Nephritis
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

9 authors.

Quentin SimonUniversité Paris Cité, Centre de recherche sur l'inflammation, INSERM UMR1149, CNRS EMR8252, Laboratoire d'Excellence Inflamex, Paris, France.
François GaillardDepartment of Nephrology, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, Paris, France.
John TchenUniversité Paris Cité, Centre de recherche sur l'inflammation, INSERM UMR1149, CNRS EMR8252, Laboratoire d'Excellence Inflamex, Paris, France.
Delphine BacheletDepartment of Biostatistical Epidemiology and Clinical research, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, INSERM CIC-EC 1425, Paris, France.
Karim SacréUniversité Paris Cité, Centre de recherche sur l'inflammation, INSERM UMR1149, CNRS EMR8252, Laboratoire d'Excellence Inflamex, Paris, France.
Katell Peoc'hUniversité Paris Cité, Centre de Recherche sur l'Inflammation, INSERM UMR1149, Laboratoire d'Excellence GR-Ex, Paris, France.
Noémie Jourde-ChicheAix-Marseille Université, C2VN, INSERM, INRAE, Marseille, France.
Eric DaugasUniversité Paris Cité, Centre de recherche sur l'inflammation, INSERM UMR1149, CNRS EMR8252, Laboratoire d'Excellence Inflamex, Paris, France.
Nicolas CharlesUniversité Paris Cité, Centre de recherche sur l'inflammation, INSERM UMR1149, CNRS EMR8252, Laboratoire d'Excellence Inflamex, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) activity decreases in some patients with end-stage kidney disease (ESKD). The impact of ESKD on the immune cell profile of SLE patients and lupus activity remains unclear. In this study, we aimed at characterizing immunologically inactive and active SLE patients undergoing dialysis therapy. Based on multi-parametric flow cytometry assays, an extensive immunophenotyping was performed on blood samples from 47 SLE patients undergoing hemodialysis, 10 non-dialyzed SLE patients with active lupus nephritis (aLN), 6 non-dialyzed patients with a history of LN currently in remission (rLN), and 20 healthy volunteers (HV) as controls (ClinicalTrials.gov Identifier: NCT03921398). The hemodialysis group was composed of 16 SLE patients with inactive disease (iHD), 22 with sustained low disease activity with a non-renal SLEDAI ≤4 (aHD≤4), and 9 highly active SLE patients (aHD>4). A factorial discriminant analysis was performed to validate the association between immune cell signatures and lupus activity. By compiling 12 cellular variables, we describe immune profiles related to highly active SLE patients or associated with both inactive and low-disease activity groups. As non-dialyzed active SLE patients, active patients undergoing hemodialysis showed a specific combination of increased numbers of circulating CD19

Indexed as

DialysisDisease activityEnd stage kidney diseaseImmunophenotypingLupus nephritisSystemic lupus erythematosus

Identifiers

PMID40453547
PMCPMC12124682

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Registered trials

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.