Evidence map›Paper›PMID 25651923›Full record

ArticleClinical and vaccine immunology : CVI2015

Use of IgG in oral fluid to monitor infants with suspected congenital toxoplasmosis.

Emmanuelle Chapey, Valeria Meroni, François Kieffer, Lina Bollani, René Ecochard, Patricia Garcia, Martine Wallon, François Peyron

Abstract readEvaluation Study
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Plasmonic gold chips for the diagnosis of Toxoplasma gondii, CMV, and rubella infections using saliva with serum detection precision.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Article
  3. Article
  4. Laboratory Diagnosis of Congenital Toxoplasmosis.Journal of clinical microbiology · 2016
    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

8 authors.

Emmanuelle ChapeyUniversité Claude Bernard Lyon 1, Service de Parasitologie, Faculté de Médecine Lyon Sud, Lyon, France.
Valeria MeroniMicrobiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
François KiefferNeonatal Unit, Hôpital Armand Trousseau, Paris, France.
Lina BollaniDepartment of Internal Medicine and Therapeutics, Università di Pavia, Pavia, Italy.
René EcochardHospices Civils de Lyon, Service de Biostatistique, Lyon, France Université de Lyon, Lyon, France Université Lyon 1, Villeurbanne, France CNRS, UMR5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, France.
Patricia GarciaDépartement de Médecine Néonatale, CHU de la Conception, Marseille, France.
Martine WallonHospices Civils de Lyon, Service de Parasitologie, Hôpital de la Croix Rousse, Lyon, France Centre de Recherche en Neurosciences de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
François PeyronUniversité Claude Bernard Lyon 1, Service de Parasitologie, Faculté de Médecine Lyon Sud, Lyon, France Hospices Civils de Lyon, Service de Parasitologie, Hôpital de la Croix Rousse, Lyon, France francois.peyron@chu-lyon.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infants born to mothers who seroconverted for toxoplasmosis during pregnancy are at risk of sequelae. In the case of a negative work-up at birth, congenital infection can be ruled out only by monitoring the disappearance of maternal immunoglobulin G (IgG) transmitted through the placenta, which can be achieved by regular blood sampling during the first year. To alleviate the discomfort of this follow-up, we developed an indirect enzyme-linked immunosorbent assay to detect specific IgG diffusing passively from the blood through the gingival epithelium by collecting oral fluid on microsponges. To assess the feasibility of the test, 212 patients were first enrolled. Levels of specific IgG in oral fluid were significantly higher in seropositive (n = 195) than in seronegative (n = 17) patients (mean optical densities, 1.145 ± 0.99 versus 0.092 ± 0.127; P < 0.0001). In a population of 93 patients <15 months of age born to mothers who displayed toxoplasmic infection during pregnancy, 70 were free of congenital infection and were followed up until their serology turned negative, and 23 were congenitally infected. The same patterns of IgG were observed in the oral fluid and sera in each group. Using a cutoff of 0.04 (optical density value), the sensitivity and specificity of the test were 67.9% and 80.3%, respectively, and the probability of not having a congenital infection when the test on oral fluid was negative was 99%. Although the performance of the test needs to be improved, oral fluid sampling appears to be a promising tool for monitoring infants with suspected congenital toxoplasmosis.

Indexed as

AdolescentAdultAntibodies, ProtozoanBody FluidsChildChild, PreschoolFemaleFollow-Up StudiesHumansImmunoglobulin GInfantInfant, NewbornMaleMiddle AgedMouthPregnancyAntibodies, ProtozoanImmunoglobulin G

Identifiers

PMID25651923
PMCPMC4375350

What OpenQuestion holds

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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.