Evidence map›Paper›PMID 21512035›Full record

ArticleMolecular & cellular proteomics : MCP2011

Identification of potential serodiagnostic and subunit vaccine antigens by antibody profiling of toxoplasmosis cases in Turkey.

Li Liang, Mert Döşkaya, Silvia Juarez, Ayşe Caner, Algis Jasinskas, Xiaolin Tan, Bettina E Hajagos, Peter J Bradley, Metin Korkmaz, Yüksel Gürüz and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  13. Identification ofClinical proteomics · 2018
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  19. Review
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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

12 authors at 3 institutions in 2 countries.

Li LiangDivision of Infectious Diseases, Department of Medicine, University of California, Irvine, CA 92697, USA.
Mert Döşkaya
Silvia Juarez
Ayşe Caner
Algis Jasinskas
Xiaolin Tan
Bettina E Hajagos
Peter J Bradley
Metin Korkmaz
Yüksel Gürüz
Philip L Felgner
D Huw Davies
University of California, Irvine · USEge University · TRUniversity of California, Los Angeles · US

Funding

Vaccines and Diagnostics TrialsU54AI065359 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI BARBOUR, ALAN G. · 2005 to 2013
$88.8M
MULTIDISCIPLINARY TRAINING IN MICROBIAL PATHOGENESIST32AI007323 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peter John Bradley · 1988 to 2026
$8.6M
The Role of Toxoplasma Rhoptries in Host Cell InfectionR01AI064616 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRADLEY, PETER JOHN · 2006 to 2016
$3.5M
Seriodiagnostic arrays for biodefense and emerging infectious diseasesR44AI058365 · NIAID · IMMPORT THERAPEUTICS, INC. · PI DAVIES, DAVID HUW · 2008 to 2010
$3.0M
Vaccinia Proteome Affinity Reagents From Phage DisplayR41AI058365 · NIAID · IMMPORT THERAPEUTICS, INC. · PI FELGNER, PHILIP LOUIS · 2004 to 2005
$995k
NIAID NIH HHS R01 AI064616NIAID NIH HHS R01AI064616NIAID NIH HHS R41 AI058365NIAID NIH HHS R44 AI058365NIAID NIH HHS R44AI058365NIAID NIH HHS T32 AI007323NIAID NIH HHS T32-AI07323NIAID NIH HHS U54 AI065359
6 · The paper itself

Abstract

Toxoplasmosis, caused by infection of the protozoan parasite Toxoplasma gondii, is associated with mild disease in healthy individuals, whereas individuals with depressed immunity may develop encephalitis, neurologic disorders, and other organ diseases. Women who develop acute toxoplasmosis during pregnancy are at risk of transmitting the infection to the fetus, which may lead to fetal damage. A diagnosis is usually confirmed by measuring IgG, or IgM where it is important to determine the onset of infection. A negative IgM result essentially excludes acute infection, whereas a positive IgM test is largely uninterpretable because IgM can persist for up to 18 months after infection. To identify antigens for improved diagnosis of acute infection, we probed protein microarrays displaying the polypeptide products of 1357 Toxoplasma exons with well-characterized sera from Turkey. The sera were classified according to conventional assays into (1) seronegative individuals with no history of T. gondii infection; (2) acute infections defined by clinical symptoms, high IgM titers, and low avidity IgG; (3) chronic/convalescent cases with high avidity IgG but persisting IgM; (iv) true chronic infections, defined by high avidity IgG and no IgM. We have identified 38 IgG target antigens and 108 IgM target antigens that can discriminate infected patients from healthy controls, one or more of which could form the basis of a 'tier-1' test to determine current or previous exposure. Of these, three IgG antigens and five IgM antigens have the potential to discriminate chronic/IgM persisting or true chronics from recent acutely infected patients (a 'tier-2' test). Our analysis of the antigens revealed several enriched features relative to the whole proteome, which include transmembrane domains, signal peptides, or predicted localization at the outer membrane. This is the first protein microarray survey of the antibody response to T. gondii, and will help in the development of improved serodiagnostics and vaccines.

Indexed as

Antibodies, ProtozoanAntigens, ProtozoanArtificial IntelligenceCase-Control StudiesComputer SimulationHumansImmunoglobulin GImmunoglobulin MModels, ImmunologicalProtein Array AnalysisROC CurveSerologic TestsToxoplasmaToxoplasmosisTurkeyVaccines, SubunitAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GImmunoglobulin MVaccines, Subunit

Identifiers

PMID21512035
PMCPMC3134070
OpenAlexW2140583333

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.