Evidence map›Paper›PMID 30952500›Full record

Trial reportVaccine2019

Kinetics of maternally-derived serogroup A, C, Y and W-specific meningococcal immunoglobulin G in Malian women and infants.

H Findlow, M D Tapia, S O Sow, F C Haidara, F Coulibaly, A M Keita, F Diallo, M Doumbia, A Traore, N Schluterman and 3 more

Open access · hybridAbstract readClinical Trial, Phase IVRandomized Controlled Trial
In one paragraph

Trial report in Vaccine, 2019. 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
0.6field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
  2. Preventing invasive meningococcal disease in early infancy.Human vaccines & immunotherapeutics · 2022
    Review
  3. Article
  4. Article
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

13 authors at 5 institutions in 3 countries.

H FindlowVaccine Evaluation Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK. Electronic address: helenfindlow@hotmail.com.
M D TapiaCenter for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, USA.
S O SowCentre pour le Développement des Vaccins, Bamako, Mali.
F C HaidaraCentre pour le Développement des Vaccins, Bamako, Mali.
F CoulibalyCentre pour le Développement des Vaccins, Bamako, Mali.
A M KeitaCentre pour le Développement des Vaccins, Bamako, Mali.
F DialloCentre pour le Développement des Vaccins, Bamako, Mali.
M DoumbiaCentre pour le Développement des Vaccins, Bamako, Mali.
A TraoreCentre pour le Développement des Vaccins, Bamako, Mali.
N SchlutermanDepartment of Epidemiology, University of Maryland, Baltimore, MD, USA.
D A ClarkDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, USA.
R BorrowVaccine Evaluation Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK.
M M LevineCenter for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, USA.
Centre Pour le Développement des Vaccins-Mali · MLUniversity of Maryland, Baltimore · USEmory University · USManchester Royal Infirmary · GBPublic Health England · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A prospective, randomised, controlled observer-blind trial measuring the efficacy and immunogenicity of trivalent influenza vaccine (TIV) and the immunogenicity of quadrivalent meningococcal conjugate vaccine (MCV) in pregnant women and their infants up to 6 months of age was conducted in Mali. Here we reported the immunogenicity of MCV, which was used as a comparator vaccine to TIV, in this population. Third-trimester pregnant Malian women were randomized to receive TIV or MCV. Blood samples were collected from women prior to vaccination, 28 days post-vaccination, at delivery and 3 and 6 months post-delivery and from infants at birth and 3 and 6 months of age. Meningococcal-specific serogroup (Men) A, C, Y and W-specific antibodies were measured by enzyme linked immunosorbent assay in a randomly selected subset of 50 mother-infant pairs where the mother had received MCV. At birth, 94.0% (47/50) of infants had MenA specific IgG levels ≥ 2 µg/mL decreasing to 72.9% and 30.4% at 3 and 6 months of age. For MenC, 81.3% (39/48) of infants had MenC specific IgG levels ≥ 2 µg/mL at birth decreasing to 29.4% and 17.8% at 3 and 6 months of age. For MenY, 89.6% (43/48) of infants had MenY specific IgG levels ≥ 2 µg/mL at birth decreasing to 64.6% and 62.5% at 3 and 6 months of age. For MenW, 89.6% (43/48) of infants had MenW specific IgG levels ≥ 2 μg/ml at birth decreasing to 62.5% and 41.7% at 3 and 6 months of age. Maternal immunization with MCV conveyed protective levels of IgG at birth through to 3 months of age in the majority of infants.

Indexed as

Immunity, Maternally-AcquiredAdultAntibodies, BacterialFemaleHumansImmunoglobulin GInfantInfant, NewbornInfluenza VaccinesKineticsMaleMaliMeningococcal InfectionsMeningococcal VaccinesPregnancyProspective StudiesAntibodies, BacterialImmunoglobulin GInfluenza VaccinesMeningococcal VaccinesVaccines, ConjugateMaternal immunizationMeningococcalVaccination

Identifiers

PMID30952500
PMCPMC6990398
OpenAlexW2926642739

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.