Evidence map›Paper›PMID 26011247›Full record

ArticlePloS one2015

Cell Based Drug Delivery: Micrococcus luteus Loaded Neutrophils as Chlorhexidine Delivery Vehicles in a Mouse Model of Liver Abscesses in Cattle.

Sebastian O Wendel, Sailesh Menon, Hamad Alshetaiwi, Tej B Shrestha, Lauren Chlebanowski, Wei-Wen Hsu, Stefan H Bossmann, Sanjeev Narayanan, Deryl L Troyer

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Biological Cells as Therapeutic Delivery Vehicles.Trends in pharmacological sciences · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Immune Cells in Cancer Therapy and Drug Delivery.Mediators of inflammation · 2016
    Review
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

9 authors at 3 institutions in 2 countries.

Sebastian O WendelDepartment of Chemical Engineering, Kansas State University, Manhattan, Kansas, United States of America.
Sailesh MenonDepartment of Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, Kansas, United States of America.
Hamad AlshetaiwiDepartment of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, United States of America; University of Ha'il, Ha'il, Saudi Arabia.
Tej B ShresthaDepartment of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, United States of America.
Lauren ChlebanowskiDepartment of Chemistry, Augustana College, Rock Island, Illinois, United States of America.
Wei-Wen HsuDepartment of Statistics, Kansas State University, Manhattan, Kansas, United States of America.
Stefan H BossmannDepartment of Chemistry, Kansas State University, Manhattan, Kansas, United States of America.
Sanjeev NarayananDepartment of Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, Kansas, United States of America.
Deryl L TroyerDepartment of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, United States of America.
Kansas State University · USAugustana College · USUniversity of Ha'il · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent WHO report on antibiotic resistances shows a dramatic increase of microbial resistance against antibiotics. With only a few new antibiotics in the pipeline, a different drug delivery approach is urgently needed. We have obtained evidence demonstrating the effectiveness of a cell based drug delivery system that utilizes the innate immune system as targeting carrier for antibacterial drugs. In this study we show the efficient loading of neutrophil granulocytes with chlorhexidine and the complete killing of E. coli as well as Fusobacterium necrophorum in in-vitro studies. Fusobacterium necrophorum causes hepatic abscesses in cattle fed high grain diets. We also show in a mouse model that this delivery system targets infections of F. necrophorum in the liver and reduces the bacterial burden by an order of magnitude from approximately 2•106 to 1•105.

Indexed as

AnimalsAnti-Infective Agents, LocalCattleCattle DiseasesCell- and Tissue-Based TherapyChlorhexidineDisease Models, AnimalDrug Delivery SystemsEscherichia coliFusobacterium necrophorumLiver AbscessMiceMicrococcus luteusNeutrophilsAnti-Infective Agents, LocalChlorhexidine

Identifiers

PMID26011247
PMCPMC4444037
OpenAlexW388921527

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.