Evidence map›Paper›PMID 22323643›Full record

ArticleJournal of the American Society of Nephrology : JASN2012

High prevalence of autoantibodies to hLAMP-2 in anti-neutrophil cytoplasmic antibody-associated vasculitis.

Renate Kain, Henko Tadema, Eoin F McKinney, Alexandra Benharkou, Ricarda Brandes, Andrea Peschel, Virginie Hubert, Tjerk Feenstra, Gürkan Sengölge, Coen Stegeman and 5 more

Open access · bronzeAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
14.6field-weighted citation impact, top 1% of its field
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

54 citing papers in PubMed, 133 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. New Biomarkers for Systemic Necrotizing Vasculitides.Journal of clinical medicine · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Review
  15. Article
  16. Article
  17. Review
  18. Animal Models of ANCA Associated Vasculitis.Frontiers in immunology · 2020
    Review
  19. Article
  20. 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

15 authors at 5 institutions in 4 countries.

Renate KainClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria. renate.kain@meduniwien.ac.at
Henko Tadema
Eoin F McKinney
Alexandra Benharkou
Ricarda Brandes
Andrea Peschel
Virginie Hubert
Tjerk Feenstra
Gürkan Sengölge
Coen Stegeman
Peter Heeringa
Paul A Lyons
Kenneth G C Smith
Cees Kallenberg
Andrew J Rees
Institute of Clinical Research · USAddenbrooke's Hospital · GBMedical University of Vienna · ATUniversity of Cambridge · GBUniversity of Groningen · NL

Funding

Medical Research Council G0400929Wellcome Trust
6 · The paper itself

Abstract

The involvement of autoantibodies to human lysosome-associated membrane protein-2 (hLAMP-2) in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is controversial because of the absence of confirmatory data subsequent to the initial reports of their high prevalence in this disease. We characterized three assays for anti-hLAMP-2 antibodies: ELISA and Western blotting assays using unglycosylated recombinant hLAMP-2 expressed in Escherichia coli, and an indirect immunofluorescence assay using stably transfected ldlD cells that expressed glycosylated full-length hLAMP-2 on the plasma membrane. The assays detected autoantibodies to hLAMP-2 in human sera reproducibly and with comparable sensitivity and the assays gave the same results in 80.5% of the test panel of 40 selected positive and negative sera. In untreated patients at presentation, the frequencies of autoantibodies to LAMP-2 were 89%, 91%, and 80%, respectively, among three groups of patients with ANCA-associated vasculitis from Vienna, Austria (n=19); Groningen, the Netherlands (n=50) and Cambridge, United Kingdom (n=53). Prevalence of LAMP-2 autoantibodies was similar in both those with myeloperoxidase-ANCA and proteinase 3-ANCA. Furthermore, we detected LAMP-2 autoantibodies in two ANCA-negative patients. LAMP-2 autoantibodies rapidly became undetectable after the initiation of immunosuppressive treatment and frequently became detectable again during clinical relapse. We conclude that when robust assays are used, circulating autoantibodies to hLAMP-2 can be detected in most European patients with ANCA-associated vasculitis. Large-scale prospective studies are now needed to determine whether they are pathogenic or merely an epiphenomenon.

Indexed as

AdultAgedAged, 80 and overAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisAustriaAutoantibodiesBlotting, WesternCase-Control StudiesEnzyme-Linked Immunosorbent AssayFluorescent Antibody Technique, IndirectHumansLysosomal-Associated Membrane Protein 2Lysosomal Membrane ProteinsMiddle AgedMyeloblastinNetherlandsAutoantibodiesLAMP2 protein, humanLysosomal-Associated Membrane Protein 2Lysosomal Membrane ProteinsMyeloblastinPeroxidase

Identifiers

PMID22323643
PMCPMC3294304
OpenAlexW2155343924

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.