Evidence map›Paper›PMID 24191022›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Development of a glycoconjugate vaccine to prevent meningitis in Africa caused by meningococcal serogroup X.

Francesca Micoli, Maria Rosaria Romano, Marta Tontini, Emilia Cappelletti, Massimiliano Gavini, Daniela Proietti, Simona Rondini, Erwin Swennen, Laura Santini, Sara Filippini and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. 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
6.6field-weighted citation impact, top 3% 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, 61 citations in OpenAlex.

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  11. Polysaccharide structure dictates mechanism of adaptive immune response to glycoconjugate vaccines.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  19. Meningococcal Vaccinations.Infectious diseases and therapy · 2016
    Review
  20. 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

20 authors at 6 institutions in 5 countries.

Francesca MicoliNovartis Vaccines Institute for Global Health, and Research, Novartis Vaccines and Diagnostics, I-53100 Siena, Italy.
Maria Rosaria Romano
Marta Tontini
Emilia Cappelletti
Massimiliano Gavini
Daniela Proietti
Simona Rondini
Erwin Swennen
Laura Santini
Sara Filippini
Cristiana Balocchi
Roberto Adamo
Gerd Pluschke
Gunnstein Norheim
Andrew Pollard
Allan Saul
Rino Rappuoli
Calman A MacLennan
Francesco Berti
Paolo Costantino
Novartis (Switzerland) · CHNovartis (Italy) · ITGlobal Vaccines (United States) · USNational Institute for Health Research · GBSwiss Tropical and Public Health Institute · CHUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neisseria meningitidis is a major cause of bacterial meningitis worldwide, especially in the African meningitis belt, and has a high associated mortality. The meningococcal serogroups A, W, and X have been responsible for epidemics and almost all cases of meningococcal meningitis in the meningitis belt over the past 12 y. Currently no vaccine is available against meningococcal X (MenX). Because the development of a new vaccine through to licensure takes many years, this leaves Africa vulnerable to new epidemics of MenX meningitis at a time when the epidemiology of meningococcal meningitis on the continent is changing rapidly, following the recent introduction of a glycoconjugate vaccine against serogroup A. Here, we report the development of candidate glycoconjugate vaccines against MenX and preclinical data from their use in animal studies. Following optimization of growth conditions of our seed MenX strain for polysaccharide (PS) production, a scalable purification process was developed yielding high amounts of pure MenX PS. Different glycoconjugates were synthesized by coupling MenX oligosaccharides of varying chain length to CRM197 as carrier protein. Analytical methods were developed for in-process control and determination of purity and consistency of the vaccines. All conjugates induced high anti-MenX PS IgG titers in mice. Antibodies were strongly bactericidal against African MenX isolates. These findings support the further development of glycoconjugate vaccines against MenX and their assessment in clinical trials to produce a vaccine against the one cause of epidemic meningococcal meningitis that currently cannot be prevented by available vaccines.

Indexed as

Africa South of the SaharaAnimalsDisease OutbreaksElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayGlycoconjugatesHumansMagnetic Resonance SpectroscopyMeningitis, MeningococcalMeningococcal VaccinesMiceNeisseria meningitidisPolysaccharides, BacterialGlycoconjugatesMeningococcal VaccinesPolysaccharides, Bacterial

Identifiers

PMID24191022
PMCPMC3839747
OpenAlexW2105664303

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.