Evidence map›Paper›PMID 39247133›Full record

ArticleVaccine: X2024

Comparison of measles plaque reduction neutralization test (PRNT) and measles virus-specific IgG ELISA for assessment of immunogenicity of measles-mumps-rubella vaccination at 5-7 months of age and maternal measles antibodies.

Dorthe Maria Vittrup, Andreas Jensen, Michelle Malon, Anne Cathrine Zimakoff, Jesper Kiehn Sørensen, Brickley Littell, Eric A F Simões, Jannet Svensson, Lone Graff Stensballe

Abstract read
In one paragraph

Article in Vaccine: X, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

9 authors.

Dorthe Maria VittrupBlegdamsvej 9, 2100 Copenhagen E, Denmark.
Andreas JensenThe National Danish University Hospital, Rigshospitalet, The Juliane Marie Center, Pediatric Department, Denmark.
Michelle MalonThe National Danish University Hospital, Rigshospitalet, The Juliane Marie Center, Pediatric Department, Denmark.
Anne Cathrine ZimakoffThe National Danish University Hospital, Rigshospitalet, The Juliane Marie Center, Pediatric Department, Denmark.
Jesper Kiehn SørensenThe National Danish University Hospital, Rigshospitalet, The Juliane Marie Center, Pediatric Department, Denmark.
Brickley LittellUniversity of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
Eric A F SimõesUniversity of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
Jannet SvenssonHerlev University Hospital, Department of Pediatrics, Denmark.
Lone Graff StensballeThe National Danish University Hospital, Rigshospitalet, The Juliane Marie Center, Pediatric Department, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Assessing the risk of measles outbreaks and identifying the susceptible parts of the population is essential to timely intervention. Infants between 6-12 months are increasingly susceptible to measles but evaluating the performance of high throughput enzyme immunoassays (ELISAs) in infants < 9 months of age is lacking. Methods: A commercially available ELISA kit (Creative Diagnostics, DEIA359) for estimating measles seroprotection was evaluated in infants 5-7 months of age. In an immunogenicity substudy in the Danish MMR trial conducted between 2019-2021, infants (and mothers at baseline) were sampled before and one month after measles-mumps-rubella vaccination (MMR) or placebo as well as one month after routine MMR at 15 months. Measles IgG ELISA was compared to the gold standard but labor-intensive measles plaque reduction neutralization test (PRNT) by Pearson and Spearman correlations and by estimating sensitivity, specificity, and positive and negative predictive values (PPV and NPV). Findings: Measles IgG levels compared to PRNT antibodies had a Pearson's correlation coefficient between 0.10-0.24. Seroprotection rates measured by ELISA in young infants were 10-14% lower than measured by PRNT. The sensitivity of the ELISA to detect serological protection compared to PRNT in the infant population differed markedly across sampling time points and was 14%, 40%, and 92% at baseline, post-intervention, and post-routine MMR, whereas the specificity was 99%, 93%, and 43%, respectively. The PPV and NPV were 68% and 87% in infants at baseline. Interpretation: The correlation between measles IgG and PRNT antibodies was low. Seroprotection was underestimated using ELISA. High-accuracy tests are needed to avoid misclassifications and practices that lead to primary or secondary vaccine failure or retention of vaccination in outbreak settings. Baseline PPV and NPV suggested some applicability of ELISA in predicting serological protection in this age group. However, PRNT may be the only accurate estimator of serological protection in young infants.

Indexed as

Diagnostic accuracyEIAELISAEnzyme immunoassayIgGImmunogenicityInfancyMeaslesMeasles IgG serologyMMRNegative Predictive ValuePositive Predictive ValuePRNPRNTSensitivitySerologySerosurveillanceSpecificity

Identifiers

PMID39247133
PMCPMC11379976

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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.