Evidence map›Paper›PMID 25483637›Full record

ArticleHuman vaccines & immunotherapeutics2014

Anti-PcrV antibody strategies against virulent Pseudomonas aeruginosa.

Teiji Sawa, Emi Ito, Vinh Huu Nguyen, Matthew Haight

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

46 citing papers in PubMed, 81 citations in OpenAlex.

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  8. Beyond Antibiotics: What the Future Holds.Antibiotics (Basel, Switzerland) · 2024
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  17. The role of bacterial translocation in sepsis: a new target for therapy.Therapeutic advances in gastroenterology · 2022
    Review
  18. Review
  19. Review
  20. Therapeutic effects of high molecular weight hyaluronic acid in severeAmerican journal of physiology. Lung cellular and molecular physiology · 2021
    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

4 authors at 4 institutions in 2 countries.

Teiji Sawaa Department of Anesthesiology ; Kyoto Prefectural University of Medicine ; Kyoto , Japan.
Emi Ito
Vinh Huu Nguyen
Matthew Haight
Fukushima Medical University · JPGeorgetown University · USKyoto Prefectural University of Medicine · JPUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudomonas aeruginosa is an opportunistic bacterial pathogen that causes fatal acute lung infections in critically ill individuals. Its pathogenesis is associated with bacterial virulence conferred by the type III secretion system (TTSS), through which P. aeruginosa causes necrosis of the lung epithelium and disseminates into the circulation, resulting in bacteremia, sepsis, and mortality. TTSS allows P. aeruginosa to directly translocate cytotoxins into eukaryotic cells, inducing cell death. The P. aeruginosa V-antigen PcrV, a homolog of the Yersinia V-antigen LcrV, is an indispensable contributor to TTS toxin translocation. Vaccination against PcrV ensures the survival of challenged mice and decreases lung inflammation and injury. Both the rabbit polyclonal anti-PcrV antibody and the murine monoclonal anti-PcrV antibody, mAb166, inhibit TTS toxin translocation. mAb166 IgG was cloned, and a molecular engineered humanized anti-PcrV IgG antigen-binding fragment, KB001, was developed for clinical use. KB001 is currently undergoing Phase-II clinical trials for ventilator-associated pneumonia in France and chronic pneumonia in cystic fibrosis in USA. In these studies, KB001 has demonstrated its safety, a favorable pharmacokinetic profile, and promising potential as a nonantibiotic strategy to reduce airway inflammation and damage in P. aeruginosa pneumonia.

Indexed as

AnimalsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialBacteremiaBacterial Secretion SystemsBacterial ToxinsImmunoglobulin Fab FragmentsImmunoglobulin GLungLung InjuryMicePneumoniaPore Forming Cytotoxic ProteinsPseudomonas aeruginosaPseudomonas InfectionsAntibodies, BacterialAntibodies, MonoclonalAntigens, Bacterialantigen V, PseudomonasBacterial Secretion SystemsBacterial ToxinsImmunoglobulin Fab FragmentsImmunoglobulin GKB001 antibodyPore Forming Cytotoxic ProteinsPseudomonas VaccinesantibodyCF, cystic fibrosisFab, fragment antigen bindingFc, fragment crystallizable regionimmunoglobulin G, IgGmAb, monoclonal antibodyMDR, multidrug resistantMDRP, multidrug resistant Pseudomonas aeruginosaP. aeruginosa, Pseudomonas aeruginosaPcrVPseudomonas aeruginosaTTSS, type III secretion systemTTS, type III secretorytype III secretion systemV-antigenVAP, ventilator-associated pneumonia

Identifiers

PMID25483637
PMCPMC5443083
OpenAlexW2065095479

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.