Evidence map›Paper›PMID 31337690›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

Apoptotic Cell-Induced, Antigen-Specific Immunoregulation to Treat Experimental Antimyeloperoxidase GN.

Poh-Yi Gan, Andrea S Godfrey, Joshua D Ooi, Kim-Maree O'Sullivan, Virginie Oudin, A Richard Kitching, Stephen R Holdsworth

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. ANCA-associated vasculitis.Nature reviews. Disease primers · 2020
    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

7 authors at 2 institutions in 2 countries.

Poh-Yi GanDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of Poh-yi.gan@monash.edu.ORCID 0000-0001-8373-7144
Andrea S GodfreyDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.
Joshua D OoiDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.
Kim-Maree O'SullivanDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.ORCID 0000-0002-3098-7948
Virginie OudinDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.
A Richard KitchingDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.ORCID 0000-0002-2713-2391
Stephen R HoldsworthDepartment of Medicine, Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia; and Departments of.
Monash University · AUPediatric Nephrology of Alabama · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyeloperoxidase (MPO)-ANCA-associated GN is a significant cause of renal failure. Manipulating autoimmunity by inducing regulatory T cells is potentially a more specific and safer therapeutic option than conventional immunosuppression.

methodsTo generate MPO-specific regulatory T cells, we used a modified protein-conjugating compound, 1-ethyl-3-(3'dimethylaminopropyl)-carbodiimide (ECDI), to couple the immunodominant MPO peptide (MPO

resultsMPO-Sp but not OVA-Sp administration increased MPO-specific, peripherally derived CD4

conclusionsThese findings in a mouse model indicate that administering apoptotic splenocytes conjugated with the immunodominant MPO peptide suppresses anti-MPO GN by inducing antigen-specific tolerance.

Indexed as

ApoptosisAnimalsAntibodies, Antineutrophil CytoplasmicAutoimmunityCD4-Positive T-LymphocytesDisease Models, AnimalFemaleGlomerulonephritisGreen Fluorescent ProteinsImmune ToleranceKidneyKidney GlomerulusMiceMice, Inbred C57BLNeutrophilsPeroxidaseAntibodies, Antineutrophil CytoplasmicGreen Fluorescent ProteinsPeroxidaseANCAend stage kidney diseasefocal segmental glomerulosclerosisglomerulonephritisimmunosuppressiontolerance

Identifiers

PMID31337690
PMCPMC6683705
OpenAlexW2963687708

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.