Evidence map›Paper›PMID 19307730›Full record

ArticleThe Journal of clinical investigation2009

Kallikrein genes are associated with lupus and glomerular basement membrane-specific antibody-induced nephritis in mice and humans.

Kui Liu, Quan-Zhen Li, Angelica M Delgado-Vega, Anna-Karin Abelson, Elena Sánchez, Jennifer A Kelly, Li Li, Yang Liu, Jinchun Zhou, Mei Yan and 30 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 134 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Transcriptome Studies in Lupus Nephritis.Archivum immunologiae et therapiae experimentalis · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. IL-17 in Renal Immunity and Autoimmunity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  17. Article
  18. Article
  19. Review
  20. Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors at 15 institutions in 8 countries.

Kui LiuDepartment of Immunology and Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390-8884, USA.
Quan-Zhen Li
Angelica M Delgado-Vega
Anna-Karin Abelson
Elena Sánchez
Jennifer A Kelly
Li Li
Yang Liu
Jinchun Zhou
Mei Yan
Qiu Ye
Shenxi Liu
Chun Xie
Xin J Zhou
Sharon A Chung
Bernardo Pons-Estel
Torsten Witte
Enrique de Ramón
Sang-Cheol Bae
Nadia Barizzone
Gian Domenico Sebastiani
Joan T Merrill
Peter K Gregersen
Gary G Gilkeson
Robert P Kimberly
Timothy J Vyse
Il Kim
Sandra D'Alfonso
Javier Martin
John B Harley
Lindsey A Criswell
Profile Study Group
Italian Collaborative Group
German Collaborative Group
Spanish Collaborative Group
Argentinian Collaborative Group
SLEGEN Consortium
Edward K Wakeland
Marta E Alarcón-Riquelme
Chandra Mohan
The University of Texas Southwestern Medical Center · USOklahoma Medical Research Foundation · USUppsala University · SECity College of San Francisco · USUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITCentro Científico Tecnólogico - Rosario · ARHammersmith Hospital · GBHanyang University · KRHanyang University Seoul Hospital · KRHospital Universitario Rey Juan Carlos · ESIRCCS San Camillo Hospital · ITMedical University of South Carolina · USMedizinische Hochschule Hannover · DENorthwell Health · USUniversity of Alabama at Birmingham · US

Funding

HLA GENE COMPLEMENTATION IN PRIMARY SJOGREN'S AND LUPUSR01AI024717 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI KOTTYAN, LEAH CLAIRE, WEIRAUCH, MATTHEW TYSON · 1987 to 2025
$7.8M
SNP Confirmation and High Throughput Genotyping CoreP30AR053483 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GUTHRIDGE, JOEL MARVIN · 2007 to 2017
$6.7M
Genetic Linkage in LupusR37AI024717 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI HARLEY, JOHN BARKER · 2005 to 2014
$4.2M
IMMUNOGENETICS--TARGET ORGAN DAMAGE IN IMMUNE NEPHRITISR01AR050812 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI MOHAN, CHANDRA · 2003 to 2012
$3.2M
NIAID NIH HHS R01 AI024717NIAID NIH HHS R37 AI024717NIAMS NIH HHS P30 AR053483NIAMS NIH HHS R01 AR050812NIAMS NIH HHS R01 AR50812
6 · The paper itself

Abstract

Immune-mediated nephritis contributes to disease in systemic lupus erythematosus, Goodpasture syndrome (caused by antibodies specific for glomerular basement membrane [anti-GBM antibodies]), and spontaneous lupus nephritis. Inbred mouse strains differ in susceptibility to anti-GBM antibody-induced and spontaneous lupus nephritis. This study sought to clarify the genetic and molecular factors that maybe responsible for enhanced immune-mediated renal disease in these models. When the kidneys of 3 mouse strains sensitive to anti-GBM antibody-induced nephritis were compared with those of 2 control strains using microarray analysis, one-fifth of the underexpressed genes belonged to the kallikrein gene family,which encodes serine esterases. Mouse strains that upregulated renal and urinary kallikreins exhibited less evidence of disease. Antagonizing the kallikrein pathway augmented disease, while agonists dampened the severity of anti-GBM antibody-induced nephritis. In addition, nephritis-sensitive mouse strains had kallikrein haplotypes that were distinct from those of control strains, including several regulatory polymorphisms,some of which were associated with functional consequences. Indeed, increased susceptibility to anti-GBM antibody-induced nephritis and spontaneous lupus nephritis was achieved by breeding mice with a genetic interval harboring the kallikrein genes onto a disease-resistant background. Finally, both human SLE and spontaneous lupus nephritis were found to be associated with kallikrein genes, particularly KLK1 and the KLK3 promoter, when DNA SNPs from independent cohorts of SLE patients and controls were compared. Collectively, these studies suggest that kallikreins are protective disease-associated genes in anti-GBM antibody-induced nephritis and lupus.

Indexed as

AnimalsBase SequenceDisease Models, AnimalDNAFemaleGene Expression ProfilingGlomerular Basement MembraneHumansKallikreinsLupus Erythematosus, SystemicLupus NephritisMiceMice, Inbred BALB CMice, Inbred DBAMolecular Sequence DataOligonucleotide Array Sequence AnalysisDNAKallikreins

Identifiers

PMID19307730
PMCPMC2662554
OpenAlexW2124886960

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.