Evidence map›Paper›PMID 35115327›Full record

ArticleJournal of the American Society of Nephrology : JASN2022

Galactose-Deficient IgA1 B cells in the Circulation of IgA Nephropathy Patients Carry Preferentially Lambda Light Chains and Mucosal Homing Receptors.

Katerina Zachova, Jana Jemelkova, Petr Kosztyu, Yukako Ohyama, Kazuo Takahashi, Josef Zadrazil, Jiri Orsag, Karel Matousovic, Dana Galuszkova, Nadezda Petejova and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
9.8field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  3. APRIL: spring forward also for IgA vasculitis nephritis in children.Pediatric nephrology (Berlin, Germany) · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 3 countries.

Katerina ZachovaDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic.
Jana JemelkovaDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic.
Petr KosztyuDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic.
Yukako OhyamaDepartment of Biomedical Molecular Sciences, School of Medicine, Fujita Health University, Nagoya, Aichi, Japan.
Kazuo TakahashiDepartment of Biomedical Molecular Sciences, School of Medicine, Fujita Health University, Nagoya, Aichi, Japan.
Josef ZadrazilDepartment of Internal Medicine III Nephrology, Rheumatology, and Endocrinology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Jiri OrsagDepartment of Internal Medicine III Nephrology, Rheumatology, and Endocrinology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Karel MatousovicDepartment of Medicine, Second School of Medicine, Charles University, Prague and University Hospital Motol, Prague, Czech Republic.
Dana GaluszkovaDepartment of Transfusion Medicine, University Hospital Olomouc, Olomouc, Czech Republic.
Nadezda PetejovaDepartment of Internal Medicine III Nephrology, Rheumatology, and Endocrinology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Jiri MesteckyDepartments of Microbiology and Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Milan RaskaDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic.ORCID 0000-0002-8572-7246
University Hospital Olomouc · CZFujita Health University · JPCharles University · CZCzech Academy of Sciences · CZPalacký University Olomouc · CZUniversity Hospital Ostrava · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIgA nephropathy (IgAN) primary glomerulonephritis is characterized by the deposition of circulating immune complexes composed of polymeric IgA1 molecules with altered O-glycans (Gd-IgA1) and anti-glycan antibodies in the kidney mesangium. The mesangial IgA deposits and serum IgA1 contain predominantly

methodsWe analyzed

resultsIn comparison to HCs and non-IgAN patients, peripheral blood surface/membrane bound (mb)-Gd-IgA1

conclusionsPeripheral blood of IgAN patients is enriched with migratory

Indexed as

Glomerulonephritis, IGAFemaleGalactoseHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MMaleGalactoseImmunoglobulin AImmunoglobulin GImmunoglobulin MB lymphocytesgalactosegalactose-deficient IgA1IgA nephropathyimmunoglobulin Aimmunoglobulin lambda chainsimmunology

Identifiers

PMID35115327
PMCPMC9063893
OpenAlexW4210696710

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.