Evidence map›Paper›PMID 21425128›Full record

ArticleArthritis and rheumatism2011

Autoantibodies to survival of motor neuron complex in patients with polymyositis: immunoprecipitation of D, E, F, and G proteins without other components of small nuclear ribonucleoproteins.

Minoru Satoh, Jason Y F Chan, Steven J Ross, Angela Ceribelli, Ilaria Cavazzana, Franco Franceschini, Yi Li, Westley H Reeves, Eric S Sobel, Edward K L Chan

Open access · greenAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  3. Systemic sclerosis associated myopathy: how to treat.Current treatment options in rheumatology · 2023
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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

10 authors at 2 institutions in 2 countries.

Minoru SatohUniversity of Florida, Gainesville, FL, USA. minoru.satoh@medicine.ufl.edu
Jason Y F Chan
Steven J Ross
Angela Ceribelli
Ilaria Cavazzana
Franco Franceschini
Yi Li
Westley H Reeves
Eric S Sobel
Edward K L Chan
University of Florida · USAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · IT

Funding

Novel Proteins Associated with SS-A/Ro in Target OrgansR01AI047859 · NIAID · UNIVERSITY OF FLORIDA · PI CHAN, EDWARD K · 2001 to 2011
$3.1M
MECHANISMS OF AUTOANTIBODY PRODUCTION IN SLER01AR040391 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI REEVES, WESTLEY H · 1991 to 2005
$1.6M
NIAID NIH HHS R01 AI047859NIAMS NIH HHS R01 AR040391NIAMS NIH HHS R01-AR-40391PHS HHS M01-R-00082
6 · The paper itself

Abstract

objectiveAutoantibodies in the systemic rheumatic diseases are clinically useful biomarkers of the diagnosis or of certain clinical characteristics. An unusual pattern of immunoprecipitation, in which the D, E, F, and G proteins of small nuclear RNPs (snRNP) but without other components of the snRNP, was noticed at the autoantibody screening. The purpose of this study was to examine the target antigens and clinical manifestations associated with this specificity.

methodsAutoantibodies in sera from 1,966 American patients (including 434 with systemic lupus erythematosus, 121 with scleroderma, 86 with polymyositis/dermatomyositis [PM/DM]) and 248 Italian patients with autoimmune diseases were screened by immunoprecipitation of (35) S-methionine-labeled cell extracts. Sera with which D, E, F, and G proteins of snRNP was immunoprecipitated, but without the other snRNP proteins, were further examined by analysis of RNA components by immunoprecipitation (silver staining), Western blotting using survival of motor neuron (SMN) complex, and immunofluorescence.

resultsThree sera that immunoprecipitated D, E, F, and G proteins without other components (U1-70K, A, B'/B, C) of the snRNP were found. Four additional proteins (130 kd, 120 kd, 38 kd, and 33 kd) were also commonly immunoprecipitated. The target antigen was identified as SMN complex (Gemin 3, Gemin 4, SMN, and Gemin 2, respectively), which plays a critical role in the assembly of snRNP. In immunofluorescence analyses, all 3 sera showed nuclear dots (Cajal bodies) and cytoplasmic staining. Only 1 serum was weakly positive on Western blotting of SMN, suggesting that these sera mainly recognize native molecule or quaternary structure. All 3 patients were white women with PM, an interesting finding, since deletion or mutation of SMN is known to cause spinal muscular atrophy.

conclusionSMN complex was identified as a new Cajal body autoantigen recognized by sera from white patients with PM. The biologic and clinical significance of anti-SMN autoantibodies will need to be clarified.

Indexed as

AdultAutoantibodiesAutoimmune DiseasesBlotting, WesternFemaleFluorescent Antibody TechniqueHumansImmunoprecipitationLupus Erythematosus, SystemicMaleMiddle AgedPolymyositisRibonucleoproteins, Small NuclearScleroderma, SystemicSMN Complex ProteinsAutoantibodiesRibonucleoproteins, Small NuclearSMN Complex Proteins

Identifiers

PMID21425128
PMCPMC3123691
OpenAlexW2082394200

What OpenQuestion holds

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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.