Evidence map›Paper›PMID 18378894›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Rational chemical design of the carbohydrate in a glycoconjugate vaccine enhances IgM-to-IgG switching.

Hilde-Kari Guttormsen, Lawrence C Paoletti, Keith G Mansfield, Wojcieck Jachymek, Harold J Jennings, Dennis L Kasper

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  7. Surface Structures of Group BMicrobiology spectrum · 2019
    Review
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  14. Development of a glycoconjugate vaccine to prevent meningitis in Africa caused by meningococcal serogroup X.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  15. Article
  16. 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

6 authors at 4 institutions in 2 countries.

Hilde-Kari GuttormsenChanning Laboratory, Department of Medicine, Brigham and Women's Hospital, and Institute for Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115, USA.
Lawrence C Paoletti
Keith G Mansfield
Wojcieck Jachymek
Harold J Jennings
Dennis L Kasper
Brigham and Women's Hospital · USInstitute for Biological Sciences · CANational Research Council Canada · CAPrimate Conservation · US

Funding

Bacterial Vaccine Antigen DiscoveryR01AI053191 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PAOLETTI, LAWRENCE C · 2004 to 2006
$887k
Nutrient Sensing and Hexokinases in T. bruceiR15AI075326 · NIAID · CLEMSON UNIVERSITY · PI MORRIS, JAMES CULVIN · 2008 to 2012
$585k
Bacterial Vaccine Antigen DiscoveryR21AI053191 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PAOLETTI, LAWRENCE C · 2003 to 2003
$298k
NIAID NIH HHS AI-053191NIAID NIH HHS AI-75326NIAID NIH HHS R01 AI053191NIAID NIH HHS R15 AI075326NIAID NIH HHS R21 AI053191
6 · The paper itself

Abstract

Many pathogens are sheltered from host immunity by surface polysaccharides that would be ideal as vaccines except that they are too similar to host antigens to be immunogenic. The production of functional IgG is a desirable response to vaccines; because IgG is the only isotype that crosses the placenta, it is of particular importance in maternal vaccines against neonatal disease due to group B Streptococcus (GBS). Clinical studies found a substantially lower proportion of IgG-relative to IgM-among antibodies elicited by conjugates prepared with purified GBS type V capsular polysaccharide (CPS) than among those evoked by CPSs of other GBS serotypes. The epitope specificity of IgG elicited in humans by a conjugate prepared with type V CPS is for chemically desialylated type V CPS (dV CPS). We studied desialylation as a mechanism for enhancing the ability of type V CPS to induce IgM-to-IgG switching. Desialylation did not affect the structural conformation of type V CPS. Rhesus macaques, whose isotype responses to GBS conjugates match those of humans, produced functionally active IgG in response to a dV CPS-tetanus toxoid conjugate (dV-TT), and 98% of neonatal mice born to dams vaccinated with dV-TT survived lethal challenge with viable GBS. Targeted chemical engineering of a carbohydrate to create a molecule less like host self may be a rational approach for improving other glycoconjugates.

Indexed as

Drug DesignAnimalsBacterial VaccinesCarbohydratesFemaleImmunoglobulin Class SwitchingImmunoglobulin GImmunoglobulin MMacaca mulattaMiceStreptococcusTreatment OutcomeVaccines, ConjugateBacterial VaccinesCarbohydratesImmunoglobulin GImmunoglobulin MVaccines, Conjugate

Identifiers

PMID18378894
PMCPMC2311338
OpenAlexW1971251821

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.