Evidence map›Paper›PMID 31287867›Full record

ArticleThe Journal of infectious diseases2019

Delayed Administration of Recombinant Plasma Gelsolin Improves Survival in a Murine Model of Penicillin-Susceptible and Penicillin-Resistant Pneumococcal Pneumonia.

Zhiping Yang, Alice Bedugnis, Susan Levinson, Mark Dinubile, Thomas Stossel, Quan Lu, Lester Kobzik

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

7 authors.

Zhiping YangDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Alice BedugnisDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Susan LevinsonBioAegis Therapeutics, North Brunswick, New Jersey.
Mark DinubileBioAegis Therapeutics, North Brunswick, New Jersey.
Thomas StosselBioAegis Therapeutics, North Brunswick, New Jersey.
Quan LuDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Lester KobzikDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.

Funding

Plasma Gelsolin as Immunotherapeutic for Antibiotic-Resistant PneumoniaR01AI125152 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI LU, QUAN · 2016 to 2018
$2.8M
NIAID NIH HHS R01 AI125152
6 · The paper itself

Abstract

Therapy to enhance host immune defenses may improve outcomes in serious infections, especially for antibiotic-resistant pathogens. Recombinant human plasma gelsolin (rhu-pGSN), a normally circulating protein, has beneficial effects in diverse preclinical models of inflammation and injury. We evaluated delayed therapy (24-48 hours after challenge) with rhu-pGSN in a mouse model of pneumococcal pneumonia. rhu-pGSN without antibiotics increased survival and reduced morbidity and weight loss after infection with either penicillin-susceptible or penicillin-resistant pneumococci (serotypes 3 and 14, respectively). rhu-pGSN improves outcomes in a highly lethal pneumococcal pneumonia model when given after a clinically relevant delay, even in the setting of antimicrobial resistance.

Indexed as

AnimalsDisease Models, AnimalGelsolinImmunologic FactorsMaleMicePneumonia, PneumococcalRecombinant ProteinsSurvival AnalysisTreatment OutcomeWeight LossGelsolinImmunologic FactorsRecombinant Proteinsantibiotic-resistanceimmunomodulationplasma gelsolinpneumonia

Identifiers

PMID31287867
PMCPMC6761947

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.