Evidence map›Paper›PMID 26000130›Full record

ArticleAuto- immunity highlights2012

Characterization for anti-cytoplasmic antibodies specificity by morphological and molecular techniques.

Claudia Alpini, Milvia Lotzniker, Serenella Valaperta, Maria Grazia Bottone, Manuela Malatesta, Alessandro Montanelli, Giampaolo Merlini

Abstract read
In one paragraph

Article in Auto- immunity highlights, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. A Phyto-mycotherapeutic Supplement, NamelyInternational journal of molecular sciences · 2024
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  3. Article
  4. Review
  5. 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

7 authors.

Claudia AlpiniServizio Analisi Chimico Cliniche Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
Milvia LotznikerLaboratorio Analisi A.O. Ospedale Civile di, Legnano, Milan Italy.
Serenella ValapertaServizio Analisi Chimico Cliniche Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
Maria Grazia BottoneDipartimento di Biologia e Biotecnologie "L.Spallanzani", Laboratorio di Biologia Cellulare e Neurobiologia, Università di Pavia, Pavia, Italy ; Istituto di Genetica Molecolare del CNR, Pavia, Italy.
Manuela MalatestaDipartimento di Biologia e Biotecnologie "L.Spallanzani", Laboratorio di Biologia Cellulare e Neurobiologia, Università di Pavia, Pavia, Italy.
Alessandro MontanelliLaboratorio Analisi IRCCS Istituto Clinico Humanitas, Rozzano, Milan, Italy.
Giampaolo MerliniServizio Analisi Chimico Cliniche Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of our study was the characterization of anti-cytoplasmic antibodies by home-made morphological and biochemical techniques. Indeed, indirect immunofluorescence (IIF) on HEp-2 cell line is not always exhaustive in relation to the complexity of the antigens involved.

methodsNine serum samples with anti-cytoplasmic antibodies (2 anti-Golgi apparatus, 3 with diffuse pattern and 4 with lysosome/endosome-like pattern) were tested with fluorescent confocal microscopy, Western blot analysis and, when necessary, with electron microscopy technique.

resultsConfirmation of the IIF staining pattern was performed in confocal microscopy by comparison with the respective antibody marker. The anti-endoplasmatic reticulum positivity was also confirmed by electron microscopy evaluation. Both anti-lysosome/endosome and anti-endoplasmatic reticulum positivity have been definitely identified by Western blot through clear reactivity with calreticulin and LC3B, respectively.

conclusionsThese results do not aim at representing a standard routine laboratory procedure. Electron microscopy evaluation cannot be proposed as a routine approach, but confocal microscopy technique may be offered in centralized reference laboratories. Newer technologies, especially multiplex immunoassay, can also lead to an easier identification of these autoantibodies, without recurring to a home-made immunoblotting. Only with a complete characterization we will be able to define the clinical relevance of anti-cytoplasmic antibodies, which are still considered as "esoteric" and not as "diagnostic" antibodies.

Indexed as

Anti-endoplasmatic reticulum antibodiesAnti-Golgi apparatus antibodiesAnti-lysosome/endosome antibodies

Identifiers

PMID26000130
PMCPMC4389067

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