Evidence map›Paper›PMID 37428339›Full record

ReviewInfectious diseases and therapy2023

Meningococcal B Immunisation in Adults and Potential Broader Immunisation Strategies: A Narrative Review.

George Kassianos, Osamah Barasheed, Victoria Abbing-Karahagopian, Mansour Khalaf, Serdar Ozturk, Angelika Banzhoff, Selim Badur

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Infectious diseases and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Genomic surveillance of invasive Neisseria meningitidis isolates circulating in Paraguay, 2009-2021.International microbiology : the official journal of the Spanish Society for Microbiology · 2025
    Observational
  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 5 countries.

George KassianosRoyal College of General Practitioners, London, UK.ORCID http://orcid.org/0000-0003-4493-3841
Osamah BarasheedKing Abdullah Medical City, Makkah, Saudi Arabia.ORCID http://orcid.org/0000-0002-9335-6019
Victoria Abbing-KarahagopianGSK, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-1987-363X
Mansour KhalafGSK, Jeddah, Saudi Arabia.ORCID http://orcid.org/0000-0001-7899-5034
Serdar OzturkGSK, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-5885-6173
Angelika BanzhoffGSK, Marburg, Germany.ORCID http://orcid.org/0000-0002-8813-282X
Selim BadurGSK, Istanbul, Turkey. selim.x.badur@gsk.com.ORCID http://orcid.org/0000-0002-0490-7203
British Orthopaedic Association · GBGGD Amsterdam · NLGlaxoSmithKline (China) · CNGlaxoSmithKline (Germany) · DEKing Abdullah Medical City · SAUniversity of Jeddah · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant vaccines against invasive meningococcal disease due to Neisseria meningitidis serogroup B (MenB) have shown substantial impact in reducing MenB disease in targeted populations. 4CMenB targets four key N. meningitidis protein antigens; human factor H binding protein (fHbp), Neisserial heparin binding antigen (NHBA), Neisseria adhesin A (NadA) and the porin A protein (PorA P1.4), with one or more of these expressed by most pathogenic MenB strains, while MenB-FHbp targets two distinct fHbp variants. While many countries recommend MenB immunisation in adults considered at high risk due to underlying medical conditions or immunosuppression, there are no recommendations for routine use in the general adult population. We reviewed the burden of MenB in adults, where, while incidence rates remain low (and far lower than in young children < 5 years of age at greatest risk), a substantial proportion of MenB cases (20% or more) is now observed in the adult population; evident in Europe, Australia, and in the United States. We also reviewed immunogenicity data in adults from clinical studies conducted during MenB vaccine development and subsequent post-licensure studies. A 2-dose schedule of 4CMenB generates hSBA titres ≥ 1:4 towards all four key vaccine target antigens in up to 98-100% of subjects. For MenB-FHbp, a ≥ fourfold rise in hSBA titres against the four primary representative test strains was observed in 70-95% of recipients following a 3-dose schedule. While this suggests potential benefits for MenB immunisation if used in adult populations, data are limited (especially for adults > 50 years) and key aspects relating to duration of protection remain unclear. Although a broader adult MenB immunisation policy could provide greater protection of the adult population, additional data are required to support policy decision-making.

Indexed as

4CMenBAdult immunizationLifelong vaccinationMenBMenB-FHbpMeningococcal diseaseNeisseria meningitidis serogroup BOutbreaksVaccines

Identifiers

PMID37428339
PMCPMC10581987
OpenAlexW4383711160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.