Evidence map›Paper›PMID 31186283›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

Human Tissue-Resident Mucosal-Associated Invariant T (MAIT) Cells in Renal Fibrosis and CKD.

Becker M P Law, Ray Wilkinson, Xiangju Wang, Katrina Kildey, Kurt Giuliani, Kenneth W Beagley, Jacobus Ungerer, Helen Healy, Andrew J Kassianos

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 54 citations in OpenAlex.

  1. T-Cell Remodeling in Renal Fibrosis: From Acute Injury to Chronic Kidney Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Review
  3. Review
  4. The Immune Microenvironment: New Therapeutic Implications in Organ Fibrosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Profibrotic MAIT17 Cells in Peritoneal Fibrosis: A New Kid on the Block?Journal of the American Society of Nephrology : JASN · 2025
    Article
  9. Article
  10. Article
  11. The immune mechanisms of the urinary tract against infections.Frontiers in cellular and infection microbiology · 2025
    Review
  12. Intestinal CXCR6Immunity · 2024
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Relevant mechanisms of MAIT cells involved in the pathogenesis of periodontitis.Frontiers in cellular and infection microbiology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Becker M P LawConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Ray WilkinsonConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Xiangju WangConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Katrina KildeyConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Kurt GiulianiConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.ORCID 0000-0001-5454-8483
Kenneth W BeagleyInstitute of Health and Biomedical Innovation/School of Biomedical Sciences, Queensland University of Technology, Brisbane, Australia; and.
Jacobus UngererConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Helen HealyConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia.
Andrew J KassianosConjoint Kidney Research Laboratory, Chemical Pathology, Pathology Queensland, Brisbane, Australia; andrew.kassianos@qimrberghofer.edu.au.
Queensland University of Technology · AURoyal Brisbane and Women's Hospital · AUThe University of Queensland · AUKidney Health Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucosal-associated invariant T (MAIT) cells represent a specialized lymphocyte population associated with chronic inflammatory disorders. Little is known, however, about MAIT cells in diseases of the kidney, including CKD.

methodsTo evaluate MAIT cells in human native kidneys with tubulointerstitial fibrosis, the hallmark of CKD, we used multicolor flow cytometry to identify, enumerate, and phenotype such cells from human kidney tissue biopsy samples, and immunofluorescence microscopy to localize these cells. We cocultured MAIT cells and human primary proximal tubular epithelial cells (PTECs) under hypoxic (1% oxygen) conditions to enable examination of mechanistic tubulointerstitial interactions.

resultsWe identified MAIT cells (CD3

conclusionsOur findings indicate that human tissue-resident MAIT cells in the kidney may contribute to the fibrotic process of CKD

Indexed as

AdultAgedAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCell CommunicationCoculture TechniquesEpithelial CellsFemaleFibrosisHumansKidneyKidney Tubules, ProximalLectins, C-TypeMaleMiddle AgedAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensLectins, C-TypeChronic inflammationchronic kidney diseasefibrosislymphocytesmucosal-associated invariant T cells

Identifiers

PMID31186283
PMCPMC6622420
OpenAlexW2949668265

What OpenQuestion holds

Textmetadata
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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.