Evidence map›Paper›PMID 30632307›Full record

ArticlePhysiological reports2019

Urinary T cells correlate with rate of renal function loss in autosomal dominant polycystic kidney disease.

Kurt A Zimmerman, Nancy M Gonzalez, Phillip Chumley, Teresa Chacana, Laurie E Harrington, Bradley K Yoder, Michal Mrug

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Inhibition of the inflammasome ameliorates orthologous polycystic kidney disease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. T-cell receptor αβImmunology and cell biology · 2023
    Article
  14. Review
  15. Primary Cilia in the Skin: Functions in Immunity and Therapeutic Potential.Frontiers in cell and developmental biology · 2021
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Kurt A ZimmermanDepartment of Cell, Developmental and Integrative Biology, The University of Alabama at Birmingham, Birmingham, Alabama.
Nancy M GonzalezDepartment of Cell, Developmental and Integrative Biology, The University of Alabama at Birmingham, Birmingham, Alabama.
Phillip ChumleyDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
Teresa ChacanaDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
Laurie E HarringtonDepartment of Cell, Developmental and Integrative Biology, The University of Alabama at Birmingham, Birmingham, Alabama.
Bradley K YoderDepartment of Cell, Developmental and Integrative Biology, The University of Alabama at Birmingham, Birmingham, Alabama.
Michal MrugDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
University of Alabama at Birmingham · US

Funding

UAB Recessive PKD Research and Translational Core CenterP30DK074038 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YODER, BRADLEY K. · 2005 to 2019
$16.6M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
Injury Response Mediated Pathogenesis in Renal CiliopathiesR01DK115752 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Bradley K. Yoder · 2018 to 2026
$4.0M
Mechanisms of C3 effects in ARPKD pathogenesisR01DK097423 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MRUG, MICHAL · 2013 to 2017
$1.6M
Pathobiology of Complement C3 effects in ADPKDI01BX002298 · VA · BIRMINGHAM VA MEDICAL CENTER · PI MRUG, MICHAL · 2014 to 2017
–
BLRD VA I01 BX002298NIAID NIH HHS T32 AI007051NIDDK NIH HHS P30 DK074038NIDDK NIH HHS R01 DK097423NIDDK NIH HHS R01 DK115752NIH HHS 2T32AI007051-38NIH HHS P30-DK-074038NIH HHS R01 DK097423NIH HHS R01 DK115752VAVA 1-I01-BX002298
6 · The paper itself

Abstract

Several innate immune response components were recognized as outcome predictors in autosomal dominant polycystic kidney disease (ADPKD) and their causative role in disease pathogenesis was confirmed in animal models. In contrast, the role of adaptive immunity in ADPKD remains relatively unexplored. Therefore, we evaluated T cell populations in kidney and urine of ADPKD patients using flow cytometry and confocal immunofluorescence microscopy approaches. These analyses revealed ADPKD-associated overall increases in the number of intrarenal CD4 and CD8 T cells that were associated with a loss of polarity in distribution between the cortex and medulla (higher in medulla vs. cortex in controls). Also, the urinary T cell-based index correlated moderately with renal function decline in a small cohort of ADPKD patients. Together, these data suggest that similar to innate immune responses, T cells participate in ADPKD pathogenesis. They also point to urinary T cells as a novel candidate marker of the disease activity in ADPKD.

Indexed as

AdultAgedAged, 80 and overCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHumansKidneyMaleMiddle AgedPolycystic Kidney, Autosomal DominantAdaptive immunitycystic kidney diseaseT cell subpopulations, eGFRurine biomarker

Identifiers

PMID30632307
PMCPMC6328912
OpenAlexW2910221823

What OpenQuestion holds

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LicenceCC BY
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.