Evidence map›Paper›PMID 26431058›Full record

ArticlePLoS neglected tropical diseases2015

Pathogen- and Host-Directed Antileishmanial Effects Mediated by Polyhexanide (PHMB).

Rebuma Firdessa, Liam Good, Maria Cecilia Amstalden, Kantaraja Chindera, Nor Fadhilah Kamaruzzaman, Martina Schultheis, Bianca Röger, Nina Hecht, Tobias A Oelschlaeger, Lorenz Meinel and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  7. Antimicrobial Polymers: The Potential Replacement of Existing Antibiotics?International journal of molecular sciences · 2019
    Review
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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

12 authors at 2 institutions in 2 countries.

Rebuma FirdessaInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
Liam GoodRoyal Veterinary College, University of London, London, United Kingdom.
Maria Cecilia AmstaldenInstitute for Pharmacy and Food Chemistry, University of Würzburg, Würzburg, Germany.
Kantaraja ChinderaRoyal Veterinary College, University of London, London, United Kingdom.
Nor Fadhilah KamaruzzamanRoyal Veterinary College, University of London, London, United Kingdom.
Martina SchultheisInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
Bianca RögerInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
Nina HechtInstitute for Pharmacy and Food Chemistry, University of Würzburg, Würzburg, Germany.
Tobias A OelschlaegerInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
Lorenz MeinelInstitute for Pharmacy and Food Chemistry, University of Würzburg, Würzburg, Germany.
Tessa LühmannInstitute for Pharmacy and Food Chemistry, University of Würzburg, Würzburg, Germany.
Heidrun MollInstitute for Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
University of Würzburg · DERoyal Veterinary College · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCutaneous leishmaniasis (CL) is a neglected tropical disease caused by protozoan parasites of the genus Leishmania. CL causes enormous suffering in many countries worldwide. There is no licensed vaccine against CL, and the chemotherapy options show limited efficacy and high toxicity. Localization of the parasites inside host cells is a barrier to most standard chemo- and immune-based interventions. Hence, novel drugs, which are safe, effective and readily accessible to third-world countries and/or drug delivery technologies for effective CL treatments are desperately needed. METHODOLOGY/PRINCIPAL

findingsHere we evaluated the antileishmanial properties and delivery potential of polyhexamethylene biguanide (PHMB; polyhexanide), a widely used antimicrobial and wound antiseptic, in the Leishmania model. PHMB showed an inherent antileishmanial activity at submicromolar concentrations. Our data revealed that PHMB kills Leishmania major (L. major) via a dual mechanism involving disruption of membrane integrity and selective chromosome condensation and damage. PHMB's DNA binding and host cell entry properties were further exploited to improve the delivery and immunomodulatory activities of unmethylated cytosine-phosphate-guanine oligodeoxynucleotides (CpG ODN). PHMB spontaneously bound CpG ODN, forming stable nanopolyplexes that enhanced uptake of CpG ODN, potentiated antimicrobial killing and reduced host cell toxicity of PHMB.

conclusionsGiven its low cost and long history of safe topical use, PHMB holds promise as a drug for CL therapy and delivery vehicle for nucleic acid immunomodulators.

Indexed as

AnimalsBiguanidesCells, CulturedFemaleLeishmania majorMiceMice, Inbred BALB COligodeoxyribonucleotidesBiguanidesCPG-oligonucleotideOligodeoxyribonucleotidespolihexanide

Identifiers

PMID26431058
PMCPMC4592236
OpenAlexW2337663237

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.