Evidence map›Paper›PMID 32586370›Full record

ArticleArthritis research & therapy2020

IgG anti-hinge antibodies against IgG4 F(ab')

Toshiyuki Ota, Shun-Ichiro Ota, Ayumi Uchino, Shuji Nagano

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

4 authors at 2 institutions in 1 country.

Toshiyuki OtaCenter for Rheumatic Diseases, Iizuka Hospital, 3-83 Yoshio-machi, Iizuka-shi, Fukuoka, 820-8505, Japan. totah2@aih-net.com.ORCID 0000-0002-4538-0137
Shun-Ichiro OtaCenter for Rheumatic Diseases, Shimonoseki City Hospital, Shimonoseki-shi, Yamaguchi, 750-0041, Japan.
Ayumi UchinoDepartment of Internal Medicine (Rheumatic Diseases Division), Iizuka Hospital, 3-83 Yoshio-machi, Iizuka-shi, Fukuoka, 820-8505, Japan.
Shuji NaganoDepartment of Internal Medicine (Rheumatic Diseases Division), Iizuka Hospital, 3-83 Yoshio-machi, Iizuka-shi, Fukuoka, 820-8505, Japan.
Aso Iizuka Hospital · JPShimonoseki City Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPepsin agglutinators, discovered over 50 years ago, have been recently referred to as anti-hinge antibodies (AHAs) because of their reaction with the IgG hinge epitope. AHAs have different reactivity for each hinge epitope generated by each protease that cleaves the hinge region at different sites. Moreover, AHAs have different reactivity against different hinge epitopes derived from each IgG subclass even when the same protease is used. Since the expression of matrix metalloproteinase-3 (MMP-3) is enhanced in rheumatoid arthritis (RA), AHA production could also be increased. The purpose of this study was to determine whether the levels of AHAs against IgG hinge epitopes produced by MMP-3 are elevated in RA.

methodsThe serum levels of IgG or IgA AHAs against the IgG1/IgG4 F(ab')

resultsSeven AHAs were statistically higher in RA patients than in HC, except IgG AHA against IgG1 F(ab')

conclusionIn RA patients, we observed diversification and amplification of AHA repertoires and diagnostic utility of the specific AHA against IgG4 F(ab')

Indexed as

Arthritis, RheumatoidPepsin AEpitopesHumansImmunoglobulin Fab FragmentsImmunoglobulin GEpitopesImmunoglobulin Fab FragmentsImmunoglobulin GPepsin AACPAAnti-hinge antibodyDiagnosisExtended epitope recognitionIgG4Matrix metalloproteinaseRheumatoid arthritisRheumatoid factor

Identifiers

PMID32586370
PMCPMC7318515
OpenAlexW3037132298

What OpenQuestion holds

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LicenceCC BY
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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.