Evidence map›Paper›PMID 23493729›Full record

ArticleThe Journal of infectious diseases2013

A peptide antagonist of CD28 signaling attenuates toxic shock and necrotizing soft-tissue infection induced by Streptococcus pyogenes.

Girish Ramachandran, Mohan E Tulapurkar, Kristina M Harris, Gila Arad, Anat Shirvan, Ronen Shemesh, Louis J Detolla, Cinzia Benazzi, Steven M Opal, Raymond Kaempfer and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Subduing the Inflammatory Cytokine Storm.International journal of molecular sciences · 2024
    Review
  5. CD8Frontiers in immunology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Host Defense Peptides as Templates for Antifungal Drug Development.Journal of fungi (Basel, Switzerland) · 2020
    Review
  15. Review
  16. Frontiers in immunology · 2019
    Article
  17. Article
  18. Review
  19. Article
  20. Superantigens hyperinduce inflammatory cytokines by enhancing the B7-2/CD28 costimulatory receptor interaction.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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

11 authors at 4 institutions in 2 countries.

Girish RamachandranCenter for Vaccine Development, University of Maryland Medical School, Baltimore, Baltimore, MD 21201, USA.
Mohan E Tulapurkar
Kristina M Harris
Gila Arad
Anat Shirvan
Ronen Shemesh
Louis J Detolla
Cinzia Benazzi
Steven M Opal
Raymond Kaempfer
Alan S Cross
Brown University · USPulmonary and Critical Care Associates · USUniversity of Bologna · ITUniversity of Maryland, Baltimore · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI WHITE, JUDITH M. · 2003 to 2013
$91.5M
NIAID NIH HHS 2U54AI057168-06NIAID NIH HHS U54 AI057168
6 · The paper itself

Abstract

Staphylococcus aureus and group A Streptococcus pyogenes (GAS) express superantigen (SAg) exotoxin proteins capable of inducing lethal shock. To induce toxicity, SAgs must bind not only to the major histocompatibility complex II molecule of antigen-presenting cells and the variable β chain of the T-cell receptor but also to the dimer interface of the T-cell costimulatory receptor CD28. Here, we show that the CD28-mimetic peptide AB103 (originally designated "p2TA") protects mice from lethal challenge with streptococcal exotoxin A, as well as from lethal GAS bacterial infection in a murine model of necrotizing soft-tissue infection. Administration of a single dose of AB103 increased survival when given up to 5 hours after infection, reduced inflammatory cytokine expression and bacterial burden at the site of infection, and improved muscle inflammation in a dose-dependent manner, without compromising cellular and humoral immunity. Thus, AB103 merits further investigation as a potential therapeutic in SAg-mediated necrotizing soft-tissue infection.

Indexed as

AnimalsAntibodies, BacterialCD28 AntigensCell ProliferationColony Count, MicrobialCytokinesDose-Response Relationship, DrugExotoxinsFemaleImmunity, CellularMiceMice, Inbred BALB CPeptidesShock, SepticSignal TransductionSoft Tissue InfectionsAntibodies, BacterialCD28 AntigensCytokinesExotoxinsPeptidesSuperantigensVirulence FactorsCD28group A S. pyogenesnecrotizing soft tissue infectionpeptide antagonistsuperantigen

Identifiers

PMID23493729
PMCPMC3654752
OpenAlexW2170754962

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.