Evidence map›Paper›PMID 27826143›Full record

ArticleEmerging microbes & infections2016

Application of a low molecular weight antifungal protein from Penicillium chrysogenum (PAF) to treat pulmonary aspergillosis in mice.

Zoltán Palicz, Tamás Gáll, Éva Leiter, Sándor Kollár, Ilona Kovács, Kornél Miszti-Blasius, István Pócsi, László Csernoch, Péter Szentesi

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. TheJournal of fungi (Basel, Switzerland) · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Antimicrobial Peptides: A New Hope in Biomedical and Pharmaceutical Fields.Frontiers in cellular and infection microbiology · 2021
    Review
  10. Review
  11. Biofungicidal Potential ofFrontiers in microbiology · 2020
    Article
  12. Review
  13. Article
  14. Antimicrobial agents and chemotherapy · 2019
    Article
  15. Article
  16. Review
  17. Article
  18. 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 1 institution in 1 country.

Zoltán PaliczDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen H-4012, Hungary.
Tamás GállDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen H-4012, Hungary.
Éva LeiterDepartment of Biotechnology and Microbiology, Faculty of Science and Technology, University of Debrecen, Debrecen H-4032, Hungary.
Sándor KollárDepartment of Pathology, Kenézy Gyula Hospital, Debrecen H-4031, Hungary.
Ilona KovácsDepartment of Pathology, Kenézy Gyula Hospital, Debrecen H-4031, Hungary.
Kornél Miszti-BlasiusDepartment of Laboratory Medicine, Medical Faculty, University of Debrecen, Debrecen H-4012, Hungary.
István PócsiDepartment of Biotechnology and Microbiology, Faculty of Science and Technology, University of Debrecen, Debrecen H-4032, Hungary.
László CsernochDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen H-4012, Hungary.
Péter SzentesiDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen H-4012, Hungary.
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PAF, a small antifungal protein from Penicillium chrysogenum, inhibits the growth of several pathogenic filamentous fungi, including members of the Aspergillus genus. PAF has been proven to have no toxic effects in vivo in mice by intranasal application. To test its efficacy against invasive pulmonary aspergillosis (IPA), experiments were carried out in mice suffering from IPA. Adult mice were immunosuppressed and then infected with Aspergillus fumigatus. After stable infection, the animals were inoculated with PAF intranasally at a concentration of 2.7 mg/kg twice per day. At this concentration-which is highly toxic in vitro to A. fumigatus-the mortality of the animals was slightly delayed but finally all animals died. Histological examinations revealed massive fungal infections in the lungs of both PAF-treated and untreated animal groups. Because intranasally administered PAF was unable to overcome IPA, modified and combined therapies were introduced. The intraperitoneal application of PAF in animals with IPA prolonged the survival of the animals only 1 day. Similar results were obtained with amphotericin B (AMB), with PAF and AMB being equally effective. Combined therapy with AMB and PAF-which are synergistic in vitro-was found to be more effective than either AMB or PAF treatment alone. As no toxic effects of PAF in mammals have been described thus far, and, moreover, there are so far no A. fumigatus strains with reported inherent or acquired PAF resistance, it is worth carrying out further studies to introduce PAF as a potential antifungal drug in human therapy.

Indexed as

Administration, IntranasalAmphotericin BAnimalsAntifungal AgentsAspergillus fumigatusDisease Models, AnimalDrug Therapy, CombinationFungal ProteinsHumansImmunocompromised HostInvasive Pulmonary AspergillosisMicePenicillium chrysogenumAmphotericin BAntifungal AgentsFungal ProteinsPAF protein, Penicillium chrysogenum

Identifiers

PMID27826143
PMCPMC5148020
OpenAlexW2550788471

What OpenQuestion holds

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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.