Evidence map›Paper›PMID 39537557›Full record

ArticleRMD open2024

Immune checkpoint molecules performance in ANCA vasculitis.

Paula Anton-Pampols, Laura Martinez Valenzuela, Loreto Fernandez Lorente, Maria Quero Ramos, Francisco Gómez Preciado, Montserrat Gomà, Joaquin Manrique, Xavier Fulladosa, Josep M Cruzado, Juan Torras and 1 more

Abstract read
In one paragraph

Article in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Immature leukocyte and plasma-induced cell death reveal subclinical immune activation in EGPA patients in remission.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  3. Article
  4. Article
  5. Review
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

11 authors.

Paula Anton-PampolsNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0003-3521-6066
Laura Martinez ValenzuelaNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain lmartinezv@bellvitgehospital.cat.ORCID 0000-0003-1230-3423
Loreto Fernandez LorenteNephrology, Navarre Hospital Complex, Pamplona, Spain.ORCID 0000-0002-0522-1131
Maria Quero RamosNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.
Francisco Gómez PreciadoNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0002-0890-0666
Montserrat GomàIDIBELL, Barcelona, Spain.
Joaquin ManriqueNephrology, Navarre Hospital Complex, Pamplona, Spain.ORCID 0000-0002-7713-1629
Xavier FulladosaNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0003-1974-9874
Josep M CruzadoNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0003-1388-8558
Juan TorrasNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0002-1135-7588
Juliana Bordignon DraibeNephrology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Spain.ORCID 0000-0002-2819-8560

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe PD-1 axis promotes protection against autoimmunity. Immune checkpoint (IC) molecules performance in anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) remains unknown. This study aims to assess the IC pathway's role in the AAV's pathophysiology.

methodsWe recruited 88 AAV from our centre as a discovery cohort (acute=42, remission=46) and 30 patients from another institution for external validation (acute=16, remission=14).Serum, urine and peripheral blood mononuclear cells (PBMCs) were collected. In vitro IC molecules production by lymphocytes was studied with and without MPO/PR3 antigen stimulus. Cell culture supernatant (SN) was obtained by centrifugation. PD-1, PD-L1 and PD-L2 concentrations were assessed in serum (s), urine (u) and SN of AAV and healthy controls (HC) using a multiplex assay. PD-1 and PD-L1's expression was analysed in six diagnostic kidney biopsies.

resultsuPD-1 and uPD-L2's concentration was lower in AAV than HC (p<0.0001, p=0.0075). Acute patients exhibited lower uPD-L2 levels compared with those in remission (p=0.036). Similarly, PBMCs showed reduced PD-1 production than HC (stimulated group p=0.04, unstimulated p=0.0074). Furthermore, patients with inflammatory renal lesions had fewer PD-1-positive interstitial cells/staining intensity compared with those with sclerotic lesions. Contradictorily, sPD-1 and sPD-L1's concentration was higher in AAV than HC (p=0.007, p<0.0001) with acute patients exhibiting elevated sPD-1 levels compared with those in remission (p=0.0051). Serum and urine findings were confirmed in the validation cohort.

conclusionsResults in urine, SN and histology suggest IC pathway abolition during acute disease restored in remission and contribute to understand PD-1 axis's role in AAV proposing it as a new biomarker of disease activity.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisProgrammed Cell Death 1 ReceptorAdultAgedB7-H1 AntigenBiomarkersCase-Control StudiesFemaleHumansImmune Checkpoint ProteinsLeukocytes, MononuclearMaleMiddle AgedProgrammed Cell Death 1 Ligand 2 ProteinB7-H1 AntigenBiomarkersCD274 protein, humanImmune Checkpoint ProteinsPDCD1LG2 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 ReceptorAutoimmunitySystemic vasculitisVasculitis

Identifiers

PMID39537557
PMCPMC11575324

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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.