Evidence map›Paper›PMID 37300748›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2023

Going Beyond Host Defence Peptides: Horizons of Chemically Engineered Peptides for Multidrug-Resistant Bacteria.

Bernardo Cavallazzi Sebold, Junjie Li, Guoying Ni, Quanlan Fu, Hejie Li, Xiaosong Liu, Tianfang Wang

Open access · hybridAbstract readReview
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Caerin 1.1/1.9 peptides controlFrontiers in microbiology · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Surveillance of vancomycin-resistant enterococci reveals shift in dominating clusters fromEuro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2024
    Article
  11. 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 at 2 institutions in 2 countries.

Bernardo Cavallazzi SeboldCentre for Bioinnovation, University of the Sunshine Coast, Maroochydore BC, QLD, 4558, Australia.
Junjie LiThe First Affiliated Hospital/Clinical Medical School, Guangdong Pharmaceutical University, Guangzhou, 510080, Guangdong, China.
Guoying NiCentre for Bioinnovation, University of the Sunshine Coast, Maroochydore BC, QLD, 4558, Australia.
Quanlan FuThe First Affiliated Hospital/Clinical Medical School, Guangdong Pharmaceutical University, Guangzhou, 510080, Guangdong, China.
Hejie LiCentre for Bioinnovation, University of the Sunshine Coast, Maroochydore BC, QLD, 4558, Australia.
Xiaosong LiuThe First Affiliated Hospital/Clinical Medical School, Guangdong Pharmaceutical University, Guangzhou, 510080, Guangdong, China. xiaosongl@yahoo.com.
Tianfang WangCentre for Bioinnovation, University of the Sunshine Coast, Maroochydore BC, QLD, 4558, Australia. twang@usc.edu.au.ORCID http://orcid.org/0000-0002-4876-7767
University of the Sunshine Coast · AUGuangdong Pharmaceutical University · CN

Funding

Foshan First People's Hospital Dengfeng 2019A008National Natural Science Foundation of China 31971355Natural Science Foundation of Guangdong Province 2020A1515010855
6 · The paper itself

Abstract

Multidrug-resistant (MDR) bacteria are considered a health threat worldwide, and this problem is set to increase over the decades. The ESKAPE, a group of six pathogens including Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacter spp. is the major source of concern due to their high death incidence and nosocomial acquired infection. Host defence peptides (HDPs) are a class of ribosomally synthesised peptides that have shown promising results in combating MDR, including the ESKAPE group, in- and outside bacterial biofilms. However, their poor pharmacokinetics in physiological mediums may impede HDPs from becoming viable clinical candidates. To circumvent this problem, chemical engineering of HDPs has been seen as an emergent approach to not only improve their pharmacokinetics but also their efficacy against pathogens. In this review, we explore several chemical modifications of HDPs that have shown promising results, especially against ESKAPE pathogens, and provide an overview of the current findings with respect to each modification.

Indexed as

Antimicrobial Cationic PeptidesEnterococcus faeciumAnti-Bacterial AgentsEnterobacterHumansKlebsiella pneumoniaePseudomonas aeruginosaAnti-Bacterial AgentsAntimicrobial Cationic Peptides

Identifiers

PMID37300748
PMCPMC10432368
OpenAlexW4380152940

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.