Evidence map›Paper›PMID 32870819›Full record

ArticleJCI insight2020

Essential role and therapeutic targeting of the glomerular endothelial glycocalyx in lupus nephritis.

Hiroyuki Kadoya, Ning Yu, Ina Maria Schiessl, Anne Riquier-Brison, Georgina Gyarmati, Dorinne Desposito, Kengo Kidokoro, Matthew J Butler, Chaim O Jacob, János Peti-Peterdi

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The endothelium response to kidney injury.Nature reviews. Nephrology · 2026
    Review
  3. Article
  4. Article
  5. Kidney Disease as a Driver of Immunosenescence: Mechanisms and Potential Interventions.Journal of the American Society of Nephrology : JASN · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Article
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  13. Article
  14. Article
  15. Article
  16. Review
  17. Endothelial cells: potential novel regulators of renal inflammation.American journal of physiology. Renal physiology · 2022
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 3 countries.

Hiroyuki KadoyaDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Ning YuDivision of Rheumatology, Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Ina Maria SchiesslDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Anne Riquier-BrisonDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Georgina GyarmatiDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Dorinne DespositoDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Kengo KidokoroDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Matthew J ButlerAcademic Renal Unit, School of Clinical Sciences, University of Bristol, Bristol, United Kingdom.
Chaim O JacobDivision of Rheumatology, Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
János Peti-PeterdiDepartment of Physiology and Neuroscience and Department of Medicine, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
University of Southern California · USUniversity of Bristol · GB

Funding

Multiphoton Imaging of the Juxtaglomerular ApparatusR01DK064324 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2004 to 2026
$8.4M
Novel regulatory mechanisms of the glomerular endotheliumR01DK123564 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2019 to 2026
$3.5M
Leukocyte NADPH Oxidase Variants in LupusR01AR072212 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JACOB, CHAIM O. · 2017 to 2022
$2.8M
Elucidation of novel gene variants predisposing to childhood and adult-onset SLER01AR057172 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JACOB, CHAIM O. · 2010 to 2014
$2.6M
Multiphoton microscope replacement for USC shared resourceS10OD021833 · OD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PETI-PETERDI, JANOS · 2017 to 2017
$600k
Medical Research Council MR/M018237/1NIAMS NIH HHS R01 AR057172NIAMS NIH HHS R01 AR072212NIDDK NIH HHS R01 DK064324NIDDK NIH HHS R01 DK123564NIH HHS S10 OD021833
6 · The paper itself

Abstract

Lupus nephritis (LN) is a major organ complication and cause of morbidity and mortality in patients with systemic lupus erythematosus (SLE). There is an unmet medical need for developing more efficient and specific, mechanism-based therapies, which depends on improved understanding of the underlying LN pathogenesis. Here we present direct visual evidence from high-power intravital imaging of the local kidney tissue microenvironment in mouse models showing that activated memory T cells originated in immune organs and the LN-specific robust accumulation of the glomerular endothelial glycocalyx played central roles in LN development. The glomerular homing of T cells was mediated via the direct binding of their CD44 to the hyaluronic acid (HA) component of the endothelial glycocalyx, and glycocalyx-degrading enzymes efficiently disrupted homing. Short-course treatment with either hyaluronidase or heparinase III provided long-term organ protection as evidenced by vastly improved albuminuria and survival rate. This glycocalyx/HA/memory T cell interaction is present in multiple SLE-affected organs and may be therapeutically targeted for SLE complications, including LN.

Indexed as

AnimalsEndothelium, VascularFemaleGlycocalyxHyaluronic AcidHyaluronoglucosaminidaseImmunologic MemoryKidney GlomerulusLupus NephritisMaleMiceMice, Inbred C57BLMice, KnockoutPolysaccharide-LyasesT-Lymphocytesheparitinsulfate lyaseHyaluronic AcidHyaluronoglucosaminidasePolysaccharide-Lyasesendothelial cellsLupusNephrologyT cells

Identifiers

PMID32870819
PMCPMC7566710
OpenAlexW3081932960

What OpenQuestion holds

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LicenceCC BY
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.