Evidence map›Paper›PMID 23249817›Full record

ArticleHuman vaccines & immunotherapeutics2013

Potential impact of the bivalent rLP2806 vaccine on Neisseria meningitidis carriage and invasive serogroup B disease.

Annaliesa S Anderson, Li Hao, Qin Jiang, Shannon L Harris, Thomas R Jones, John L Perez, Laura York, Joseph Eiden, Kathrin U Jansen

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Annaliesa S AndersonPfizer Vaccine Research; Pearl River, NY USA.
Li Hao
Qin Jiang
Shannon L Harris
Thomas R Jones
John L Perez
Laura York
Joseph Eiden
Kathrin U Jansen
Pearl River Community College · USPfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asymptomatic throat carriage of Neisseria meningitidis is common in healthy individuals. In unusual cases, the bacteria become invasive, resulting in life-threatening disease. Effective meningococcal serogroup B (MnB) vaccines should provide broad protection against disease-causing strains and may confer indirect protection by impacting carriage and subsequent transmission. Factor H binding proteins (fHBPs), components of MnB vaccines in development, are classified into two immunologically distinct subfamilies (A and B). fHBP variants of MnB strains carried by adolescents are similar to those detected in infants with MnB disease. A vaccine containing subfamily A and B fHBP variants elicited bactericidal antibody responses (titers ≥ 1:4) against MnB strains expressing fHBP variants common to carriage strains and strains that cause disease in adolescents and infants in 75-100% of adolescent study subjects. This suggests that the bivalent fHBP vaccine has the potential to provide protection against invasive MnB strains and interrupt meningococcal carriage, which may also reduce infant MnB disease.

Indexed as

AdolescentAntibodies, BacterialAntigens, BacterialBacteremiaBacterial ProteinsBlood Bactericidal ActivityCarrier StateFemaleHumansInfantInfant, NewbornMaleMeningococcal InfectionsMeningococcal VaccinesNeisseria meningitidis, Serogroup BRecombinant ProteinsAntibodies, BacterialAntigens, BacterialBacterial Proteinsfactor H-binding protein, Neisseria meningitidisMeningococcal VaccinesRecombinant ProteinsVaccines, Syntheticfactor H binding proteinherd protectionmeningococcal carriagemeningococcal vaccinesNeisseria meningitidisserogroup B

Identifiers

PMID23249817
PMCPMC3891702
OpenAlexW1965978025

What OpenQuestion holds

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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.