Evidence map›Paper›PMID 20375242›Full record

ArticleClinical and vaccine immunology : CVI2010

Characterization of fHbp, nhba (gna2132), nadA, porA, and sequence type in group B meningococcal case isolates collected in England and Wales during January 2008 and potential coverage of an investigational group B meningococcal vaccine.

Jay Lucidarme, Maurizio Comanducci, Jamie Findlow, Stephen J Gray, Edward B Kaczmarski, Malcolm Guiver, Pamela J Vallely, Philipp Oster, Mariagrazia Pizza, Stefania Bambini and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Molecular characterization of invasiveFrontiers in cellular and infection microbiology · 2023
    Article
  3. Product review on the IMD serogroup B vaccine Bexsero®.Human vaccines & immunotherapeutics · 2022
    Article
  4. Meningococcal Urethritis: Old and New.Journal of clinical microbiology · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cocrystal structure of meningococcal factor H binding protein variant 3 reveals a new crossprotective epitope recognized by human mAb 1E6.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  10. Article
  11. Crystal structures of human Fabs targeting the Bexsero meningococcal vaccine antigen NHBA.Acta crystallographica. Section F, Structural biology communications · 2017
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Neisseria adhesin A variation and revised nomenclature scheme.Clinical and vaccine immunology : CVI · 2014
    Article
  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

12 authors at 2 institutions in 2 countries.

Jay LucidarmeVaccine Evaluation Unit, Health Protection Agency, P.O. Box 209, Floor 2, Clinical Sciences Building 2, Manchester Royal Infirmary, Oxford Road, Manchester M139WZ, United Kingdom. jay.lucidarme@hpa.org.uk
Maurizio Comanducci
Jamie Findlow
Stephen J Gray
Edward B Kaczmarski
Malcolm Guiver
Pamela J Vallely
Philipp Oster
Mariagrazia Pizza
Stefania Bambini
Alessandro Muzzi
Ray Borrow
University of Manchester · GBNovartis (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invasive disease caused by meningococcal capsular groups A, C, W-135, and Y is now preventable by means of glycoconjugate vaccines that target their respective polysaccharide capsules. The capsule of group B meningococci (MenB) is poorly immunogenic and may induce autoimmunity. Vaccines based on the major immunodominant surface porin, PorA, are effective against clonal epidemics but, thus far, have a limited scope of coverage against the wider MenB population at large. In an alternative approach, the first-generation, investigational, recombinant MenB (rMenB) plus outer membrane vesicle (OMV) (rMenB-OMV) vaccine contains a number of relatively conserved surface proteins, fHBP, NHBA (previously GNA2132), and NadA, alongside PorA P1.4-containing OMVs from the New Zealand MeNZB vaccine. MenB currently accounts for approximately 90% of cases of meningococcal disease in England and Wales. To assess potential rMenB-OMV vaccine coverage of pathogenic MenB isolates within this region, all English and Welsh MenB case isolates from January 2008 (n = 87) were genetically characterized with respect to fHBP, NHBA, NadA, and PorA. Alleles for fHbp, nhba, and porA were identified in all of the isolates, of which 22% were also found to harbor nadA alleles. On the basis of genotypic data and predicted immunological cross-reactivity, the potential level of rMenB-OMV vaccine coverage in England and Wales ranges from 66% to 100%.

Indexed as

Adhesins, BacterialAntigens, BacterialBacterial ProteinsPorinsAllelesAmino Acid SequenceCross ReactionsEnglandGenotypeHumansMeningococcal InfectionsMeningococcal VaccinesMolecular Sequence DataNeisseria meningitidis, Serogroup BPolymerase Chain ReactionSequence AlignmentAdhesins, BacterialAntigens, BacterialBacterial Proteinsfactor H-binding protein, Neisseria meningitidisMeningococcal VaccinesNadA protein, Neisseria meningitidisporin protein, NeisseriaPorinsVaccines, Synthetic

Identifiers

PMID20375242
PMCPMC2884420
OpenAlexW2158583653

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.