Evidence map›Paper›PMID 26169269›Full record

ArticleInfection and immunity2015

Monoclonal Antibodies of a Diverse Isotype Induced by an O-Antigen Glycoconjugate Vaccine Mediate In Vitro and In Vivo Killing of African Invasive Nontyphoidal Salmonella.

Yun Shan Goh, Simon Clare, Francesca Micoli, Allan Saul, Pietro Mastroeni, Calman A MacLennan

Open access · hybridAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

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  13. Antibodies and Protection in SystemicInfection and immunity · 2020
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  15. Immunogenicity and protective efficacy againstHuman vaccines & immunotherapeutics · 2019
    Article
  16. Article
  17. Article
  18. Comparative immunogenicity and efficacy of equivalent outer membrane vesicle and glycoconjugate vaccines against nontyphoidalProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  19. Review
  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

6 authors at 4 institutions in 3 countries.

Yun Shan GohWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom Singapore Immunology Network, Agency for Science, Technology and Research, Biopolis, Singapore.
Simon ClareWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
Francesca MicoliSclavo Behring Vaccines Institute for Global Health, a GlaxoSmithKline Company, Siena, Italy.
Allan SaulSclavo Behring Vaccines Institute for Global Health, a GlaxoSmithKline Company, Siena, Italy.
Pietro MastroeniWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Calman A MacLennanWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom School of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom calman.maclennan@ndm.ox.ac.uk.
GlaxoSmithKline (Italy) · ITWellcome Sanger Institute · GBUniversity of Birmingham · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I002189/1Medical Research Council G0001245Wellcome Trust
6 · The paper itself

Abstract

Nontyphoidal Salmonella (NTS), particularly Salmonella enterica serovars Typhimurium and Enteritidis, is responsible for a major global burden of invasive disease with high associated case-fatality rates. We recently reported the development of a candidate O-antigen-CRM197 glycoconjugate vaccine against S. Typhimurium. Here, using a panel of mouse monoclonal antibodies generated by the vaccine, we examined the relative efficiency of different antibody isotypes specific for the O:4 antigen of S. Typhimurium to effect in vitro and in vivo killing of the invasive African S. Typhimurium strain D23580. All O:4-specific antibody isotypes could mediate cell-free killing and phagocytosis of S. Typhimurium by mouse blood cells. Opsonization of Salmonella with O:4-specific IgA, IgG1, IgG2a, and IgG2b, but not IgM, resulted in cell-dependent bacterial killing. At high concentrations, O:4-specific antibodies inhibited both cell-free complement-mediated and cell-dependent opsonophagocytic killing of S. Typhimurium in vitro. Using passive immunization in mice, the O:4-specific antibodies provided in vivo functional activity by decreasing the bacterial load in the blood and tissues, with IgG2a and IgG2b being the most effective isotypes. In conclusion, an O-antigen-CRM197 glycoconjugate vaccine can induce O-antigen-specific antibodies of different isotypes that exert in vitro and in vivo killing of S. Typhimurium.

Indexed as

AnimalsAntibodies, BacterialAntibodies, MonoclonalDisease Models, AnimalFemaleHumansImmunoglobulin IsotypesMiceMice, Inbred C57BLMice, KnockoutO AntigensSalmonella entericaSalmonella InfectionsSalmonella VaccinesAntibodies, BacterialAntibodies, MonoclonalImmunoglobulin IsotypesO AntigensSalmonella Vaccines

Identifiers

PMID26169269
PMCPMC4534659
OpenAlexW1907272125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.