Evidence map›Paper›PMID 22496494›Full record

ArticleClinical and vaccine immunology : CVI2012

Peptide microarray analysis of in silico-predicted epitopes for serological diagnosis of Toxoplasma gondii infection in humans.

Pavlo Maksimov, Johannes Zerweck, Aline Maksimov, Andrea Hotop, Uwe Gross, Uwe Pleyer, Katrin Spekker, Walter Däubener, Sandra Werdermann, Olaf Niederstrasser and 5 more

Open access · diamondAbstract readEvaluation Study
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Serotyping, a challenging approach forFrontiers in medicine · 2023
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  7. Limited value of current and newFrontiers in parasitology · 2023
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  8. Review
  9. Identification of Oocyst-DrivenMicroorganisms · 2021
    Review
  10. Frontiers in cellular and infection microbiology · 2021
    Article
  11. Review
  12. Key Limitations and New Insights Into theFrontiers in cellular and infection microbiology · 2020
    Review
  13. Serotyping ofFrontiers in cellular and infection microbiology · 2019
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
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

15 authors at 8 institutions in 1 country.

Pavlo MaksimovFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Wusterhausen, Germany. pavlo.maksimov@fli.bund.de
Johannes Zerweck
Aline Maksimov
Andrea Hotop
Uwe Gross
Uwe Pleyer
Katrin Spekker
Walter Däubener
Sandra Werdermann
Olaf Niederstrasser
Eckhardt Petri
Marc Mertens
Rainer G Ulrich
Franz J Conraths
Gereon Schares
Friedrich-Loeffler-Institut · DEHeinrich Heine University Düsseldorf · DEUniversitätsmedizin Göttingen · DECharité - Universitätsmedizin Berlin · DEHelios Hospital Bad Saarow · DEInstitut für Soziale Arbeit · DEJPT Peptide Technologies (Germany) · DENovartis (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxoplasma gondii infections occur worldwide in humans and animals. In immunocompromised or prenatally infected humans, T. gondii can cause severe clinical symptoms. The identification of specific epitopes on T. gondii antigens is essential for the improvement and standardization of the serological diagnosis of toxoplasmosis. We selected 20 peptides mimicking linear epitopes on GRA1, GRA2, GRA4, and MIC3 antigenic T. gondii proteins in silico using the software ABCpred. A further 18 peptides representing previously published epitopes derived from GRA1, SAG1, NTPase1, and NTPase2 antigens were added to the panel. A peptide microarray assay was established to prove the diagnostic performance of the selected peptides with human serum samples. Seropositive human serum samples (n = 184) were collected from patients presenting with acute toxoplasmosis (n = 21), latent T. gondii infection (n = 53), and inactive ocular toxoplasmosis (n = 10) and from seropositive forest workers (n = 100). To adjust the cutoff values for each peptide, sera from seronegative forest workers (n = 75) and patients (n = 65) were used. Univariate logistic regression suggested the significant diagnostic potential of eight novel and two previously published peptides. A test based on these peptides had an overall diagnostic sensitivity of 69% (100% in ocular toxoplasmosis patients, 86% in acutely infected patients, 81% in latently infected patients, and 57% in seropositive forest workers). The analysis of seronegative sera performed with these peptides revealed a diagnostic specificity of 84%. The results of our study suggest that the use of a bioinformatic approach for epitope prediction in combination with peptide microarray testing is a powerful method for the selection of T. gondii epitopes as candidate antigens for serological diagnosis.

Indexed as

Protein Array AnalysisAntibodies, ProtozoanAntigens, ProtozoanComputational BiologyEpitopesHumansImmunoassayProtozoan ProteinsSensitivity and SpecificityToxoplasmaToxoplasmosisAntibodies, ProtozoanAntigens, ProtozoanEpitopesProtozoan Proteins

Identifiers

PMID22496494
PMCPMC3370440
OpenAlexW2167015342

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.