Evidence map›Paper›PMID 12379678›Full record

ArticleInfection and immunity2002

Sequential immunization with vesicles prepared from heterologous Neisseria meningitidis strains elicits broadly protective serum antibodies to group B strains.

Gregory R Moe, Patricia Zuno-Mitchell, Samantha N Hammond, Dan M Granoff

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Protective effect ofMicrobiology spectrum · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Sequential Vaccination With HeterologousFrontiers in immunology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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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

4 authors.

Gregory R MoeChildren's Hospital Oakland Research Institute, Oakland, California 94609-1673, USA.
Patricia Zuno-Mitchell
Samantha N Hammond
Dan M Granoff

Funding

Novel vaccine strategies for prevention of N. meningitidis group B diseaseR01AI046464 · NIAID · OMVAX, INC. · PI MOE, GREGORY ROBERT · 2000 to 2024
$12.1M
MIMETICS OF CAPSULAR EPITOPES OF NEISSERIA MENINGITIDISR01AI045642 · NIAID · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI MOE, GREGORY R · 2000 to 2004
$2.9M
NIAID NIH HHS AI46464NIAID NIH HHS R01 AI045642NIAID NIH HHS R01 AI046464NIAID NIH HHS R01 AI45642
6 · The paper itself

Abstract

The capsular polysaccharide of Neisseria meningitidis group B is an autoantigen, whereas noncapsular antigens are highly variable. These factors present formidable challenges for development of a broadly protective and safe group B vaccine. Mice and guinea pigs were sequentially immunized with three doses of micovesicles or outer membrane vesicles prepared from three meningococcal strains that were each antigenically heterologous with respect to the two major porin proteins, PorA and PorB, and the group capsular polysaccharide. The resulting antisera conferred passive protection against meningococcal group B bacteremia in infant rats and elicited complement-mediated bactericidal activity against genetically diverse group B strains that were either homologous or heterologous with respect to PorA of the strains used to prepare the vaccine. By using knockout strains, a portion of the bactericidal antibody was directed against the highly conserved protein, neisserial surface protein A (NspA). Further, an anti-NspA monoclonal antibody elicited by the sequential immunization was highly bactericidal against strains that were previously shown to be resistant to bacteriolysis by anti-NspA antibodies produced by immunization with recombinant NspA. Sequential immunization with heterologous vesicle preparations offers a novel approach to eliciting broadly protective immunity against N. meningitidis strains. An NspA-based vaccine prepared from protein expressed by Neisseria also may be more effective than the corresponding recombinant protein made in Escherichia coli.

Indexed as

AnimalsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialBacterial CapsulesBacterial Outer Membrane ProteinsBlood Bactericidal ActivityFemaleGuinea PigsImmune SeraImmunizationMeningococcal VaccinesMiceNeisseria meningitidisPorinsRatsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialBacterial Outer Membrane ProteinsImmune SeraMeningococcal VaccinesNspA protein, Neisseriaporin protein, NeisseriaPorins

Identifiers

PMID12379678
PMCPMC130404
OpenAlexW2044342990

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.