Evidence map›Paper›PMID 37701440›Full record

ArticleFrontiers in immunology2023

Comprehensive autoantibody profiling in systemic autoimmunity by a highly-sensitive multiplex protein array.

Ai Kuzumi, Yuta Norimatsu, Kazuki M Matsuda, Chihiro Ono, Taishi Okumura, Emi Kogo, Naoki Goshima, Takemichi Fukasawa, Natsumi Fushida, Motoki Horii and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. 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
7.1field-weighted citation impact, top 2% 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, 33 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Ai KuzumiDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Yuta NorimatsuDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Kazuki M MatsudaDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Chihiro OnoProteoBridge Corporation, Tokyo, Japan.
Taishi OkumuraProteoBridge Corporation, Tokyo, Japan.
Emi KogoProteoBridge Corporation, Tokyo, Japan.
Naoki GoshimaProteoBridge Corporation, Tokyo, Japan.
Takemichi FukasawaDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Natsumi FushidaDepartment of Dermatology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
Motoki HoriiDepartment of Dermatology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
Takashi YamashitaDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Asako Yoshizaki-OgawaDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Kei YamaguchiProteoBridge Corporation, Tokyo, Japan.
Takashi MatsushitaDepartment of Dermatology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
Shinichi SatoDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Ayumi YoshizakiDepartment of Dermatology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
The University of Tokyo · JPKanazawa University · JPNational Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comprehensive autoantibody evaluation is essential for the management of autoimmune disorders. However, conventional methods suffer from poor sensitivity, low throughput, or limited availability. Here, using a proteome-wide human cDNA library, we developed a novel multiplex protein assay (autoantibody array assay; A-Cube) covering 65 antigens of 43 autoantibodies that are associated with systemic sclerosis (SSc) and polymyositis/dermatomyositis (PM/DM). The performance of A-Cube was validated against immunoprecipitation and established enzyme-linked immunosorbent assay. Further, through an evaluation of serum samples from 357 SSc and 172 PM/DM patients, A-Cube meticulously illustrated a diverse autoantibody landscape in these diseases. The wide coverage and high sensitivity of A-Cube also allowed the overlap and correlation analysis between multiple autoantibodies. Lastly, reviewing the cases with distinct autoantibody profiles by A-Cube underscored the importance of thorough autoantibody detection. Together, these data highlighted the utility of A-Cube as well as the clinical relevance of autoantibody profiles in SSc and PM/DM.

Indexed as

Autoimmune DiseasesDermatomyositisScleroderma, SystemicAutoantibodiesAutoimmunityHumansProtein Array AnalysisAutoantibodiesautoantibodydermatomyositispolymyositisproteomicssystemic sclerosis

Identifiers

PMID37701440
PMCPMC10493387
OpenAlexW4386216960

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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.