Evidence map›Paper›PMID 17101655›Full record

ArticleInfection and immunity2007

Affinity-purified human immunoglobulin G that binds a lacto-N-neotetraose-dependent lipooligosaccharide structure is bactericidal for serogroup B Neisseria meningitidis.

Michele M Estabrook, Gary A Jarvis, J McLeod Griffiss

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Frontiers in immunology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review of meningococcal group B vaccines.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2010
    Review
  13. Article
  14. Phase I safety and immunogenicity study of a Brazilian serogroup B vaccine.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    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

3 authors at 2 institutions in 1 country.

Michele M EstabrookDepartment of Pediatrics, Laboratory Medicine, University of California at San Francisco, San Francisco, California 94121, USA. stabrookm@peds.ucsf.edu
Gary A Jarvis
J McLeod Griffiss
University of California, San Francisco · USPediatrics and Genetics · US

Funding

Bacterial STI and Innate Immunity in HIV SusceptibilityR01AI063927 · NIAID · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI JARVIS, GARY A · 2005 to 2009
$2.9M
A Meningococcal LOS VaccineR01AI053728 · NIAID · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI GRIFFISS, JOHN MCLEOD · 2003 to 2009
$2.1M
NIAID NIH HHS AI053728NIAID NIH HHS AI063927NIAID NIH HHS R01 AI053728NIAID NIH HHS R01 AI063927
6 · The paper itself

Abstract

Despite technological advances, no vaccine to prevent serogroup B meningococcal disease is available. The failure to develop a vaccine has shifted the focus to an alternative outer membrane structure, lipooligosaccharide (LOS), because disseminated disease induces bactericidal immunoglobulin G (IgG) that binds LOS. The purpose of this study was to identify the LOS structure(s) that induces human bactericidal IgG by purification and characterization of these antibodies. Human LOS IgG antibodies were affinity purified by passage of intravenous immunoglobulin through purified, type-specific LOS having a known structure coupled to epoxy-activated Sepharose 6B. Pathogenic group B strains representing the major LOS serotypes were used to examine the binding and bactericidal activities of four LOS-specific IgG preparations. All four LOS-specific IgG preparations bound to strains expressing homologous, as well as heterologous, LOS serotypes as determined by flow cytometry and an enzyme-linked immunosorbent assay. With human complement, IgG that was purified with L7 LOS was bactericidal for strains expressing L3,7 and L2,4 LOS, serotypes expressed by the majority of disease-associated group B and C meningococci. In conclusion, we purified human LOS-specific IgG that binds meningococci across LOS glycose-specific serotypes. An antigen that is dependent on the glycose lacto-N-neotetraose induces IgG in humans that is bactericidal for L2, L3, L4, and L7 strains. A vaccine containing this antigen would have the potential to protect against the vast majority of group B meningococcal strains.

Indexed as

Antibodies, BacterialAntigens, BacterialChromatography, AffinityEnzyme-Linked Immunosorbent AssayFlow CytometryHumansImmunoglobulin GImmunoglobulins, IntravenousLipopolysaccharidesMicrobial ViabilityNeisseria meningitidis, Serogroup BOligosaccharidesProtein BindingAntibodies, BacterialAntigens, BacterialImmunoglobulin GImmunoglobulins, Intravenouslacto-N-neotetraoselipid-linked oligosaccharidesLipopolysaccharidesOligosaccharides

Identifiers

PMID17101655
PMCPMC1828497
OpenAlexW2169078527

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.