Evidence map›Paper›PMID 31517054›Full record

ArticleScience advances2019

Antibodies to the conserved region of the M protein and a streptococcal superantigen cooperatively resolve toxic shock-like syndrome in HLA-humanized mice.

Manisha Pandey, Ainslie Calcutt, Victoria Ozberk, Zhenjun Chen, Matthew Croxen, Jessica Powell, Emma Langshaw, Jamie-Lee Mills, Freda E-C Jen, James McCluskey and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. 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
1.8field-weighted citation impact, top 15% 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, 19 citations in OpenAlex.

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  9. A worldwide population ofThe Lancet regional health. Western Pacific · 2024
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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

13 authors at 4 institutions in 2 countries.

Manisha PandeyInstitute for Glycomics, Griffith University, Gold Coast, Australia.ORCID 0000-0002-4151-699X
Ainslie CalcuttInstitute for Glycomics, Griffith University, Gold Coast, Australia.
Victoria OzberkInstitute for Glycomics, Griffith University, Gold Coast, Australia.
Zhenjun ChenDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Australia.ORCID 0000-0003-1205-683X
Matthew CroxenDivision of Diagnostic and Applied Microbiology, Department of Laboratory Medicine and Pathology, University of Alberta and ProvLab, Edmonton, Canada.ORCID 0000-0002-9564-7952
Jessica PowellInstitute for Glycomics, Griffith University, Gold Coast, Australia.ORCID 0000-0001-5120-7675
Emma LangshawInstitute for Glycomics, Griffith University, Gold Coast, Australia.
Jamie-Lee MillsInstitute for Glycomics, Griffith University, Gold Coast, Australia.ORCID 0000-0003-4547-4579
Freda E-C JenInstitute for Glycomics, Griffith University, Gold Coast, Australia.
James McCluskeyDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Australia.ORCID 0000-0002-8597-815X
Jenny RobsonSullivan and Nicolaides Pathology, Brisbane, Australia.
Gregory J TyrrellDivision of Diagnostic and Applied Microbiology, Department of Laboratory Medicine and Pathology, University of Alberta and ProvLab, Edmonton, Canada.
Michael F GoodInstitute for Glycomics, Griffith University, Gold Coast, Australia.ORCID 0000-0001-8212-248X
Griffith University · AUThe University of Melbourne · AUUniversity of Alberta · CASullivan Nicolaides Pathology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invasive streptococcal disease (ISD) and toxic shock syndrome (STSS) result in over 160,000 deaths each year. We modelled these in HLA-transgenic mice infected with a clinically lethal isolate expressing Streptococcal pyrogenic exotoxin (Spe) C and demonstrate that both SpeC and streptococcal M protein, acting cooperatively, are required for disease. Vaccination with a conserved M protein peptide, J8, protects against STSS by causing a dramatic reduction in bacterial burden associated with the absence of SpeC and inflammatory cytokines in the blood. Furthermore, passive immunotherapy with antibodies to J8 quickly resolves established disease by clearing the infection and ablating the inflammatory activity of the M protein, which is further enhanced by addition of SpeC antibodies. Analysis of 77 recent isolates of

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsBacterial ProteinsCarrier ProteinsExotoxinsHLA AntigensHumansMiceMice, Inbred BALB CMice, TransgenicShock, SepticStreptococcal InfectionsStreptococcus pyogenesSuperantigensAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsBacterial ProteinsCarrier Proteinserythrogenic toxinExotoxinsHLA Antigensstreptococcal M proteinSuperantigens

Identifiers

PMID31517054
PMCPMC6726444
OpenAlexW2971636403

What OpenQuestion holds

Textmetadata
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.