Evidence map›Paper›PMID 35746772›Full record

ArticleViruses2022

Photodynamic Inactivation of SARS-CoV-2 Infectivity and Antiviral Treatment Effects In Vitro.

Svitlana Ziganshyna, Grit Szczepankiewicz, Mathias Kuehnert, Agnes Schulze, Uwe Gerd Liebert, Corinna Pietsch, Volker Eulenburg, Robert Werdehausen

Abstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Targeted photodynamic neutralization of SARS-CoV-2 mediated by singlet oxygen.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  8. Review
  9. Near-Infrared Dyes: Towards Broad-Spectrum Antivirals.International journal of molecular sciences · 2022
    Review
  10. 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

8 authors.

Svitlana ZiganshynaDepartment of Anaesthesiology and Intensive Care, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.
Grit SzczepankiewiczMedical Faculty, Institute of Medical Microbiology and Virology, University of Leipzig, 04103 Leipzig, Germany.
Mathias KuehnertLeibniz Institute of Surface Engineering (IOM), 04318 Leipzig, Germany.
Agnes SchulzeLeibniz Institute of Surface Engineering (IOM), 04318 Leipzig, Germany.ORCID 0000-0003-1316-1367
Uwe Gerd LiebertMedical Faculty, Institute of Medical Microbiology and Virology, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0002-5129-0875
Corinna PietschMedical Faculty, Institute of Medical Microbiology and Virology, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0001-6029-3368
Volker EulenburgDepartment of Anaesthesiology and Intensive Care, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0002-4878-5746
Robert WerdehausenDepartment of Anaesthesiology and Intensive Care, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0002-1176-161X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite available vaccines, antibodies and antiviral agents, the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic still continues to cause severe disease and death. Current treatment options are limited, and emerging new mutations are a challenge. Thus, novel treatments and measures for prevention of viral infections are urgently required. Photodynamic inactivation (PDI) is a potential treatment for infections by a broad variety of critical pathogens, including viruses. We explored the infectiousness of clinical SARS-CoV-2 isolates in Vero cell cultures after PDI-treatment, using the photosensitizer Tetrahydroporphyrin-tetratosylate (THPTS) and near-infrared light. Replication of viral RNA (qPCR), viral cytopathic effects (microscopy) and mitochondrial activity were assessed. PDI of virus suspension with 1 µM THPTS before infection resulted in a reduction of detectable viral RNA by 3 log levels at day 3 and 6 after infection to similar levels as in previously heat-inactivated virions (<99.9%; p < 0.05). Mitochondrial activity, which was significantly reduced by viral infection, was markedly increased by PDI to levels similar to uninfected cell cultures. When applying THPTS-based PDI after infection, a single treatment had a virus load-reducing effect only at a higher concentration (3 µM) and reduced cell viability in terms of PDI-induced toxicity. Repeated PDI with 0.3 µM THPTS every 4 h for 3 d after infection reduced the viral load by more than 99.9% (p < 0.05), while cell viability was maintained. Our data demonstrate that THPTS-based antiviral PDI might constitute a promising approach for inactivation of SARS-CoV-2. Further testing will demonstrate if THPTS is also suitable to reduce the viral load in vivo.

Indexed as

COVID-19 Drug TreatmentSARS-CoV-2AnimalsAntiviral AgentsChlorocebus aethiopsPandemicsRNA, ViralVero CellsAntiviral AgentsRNA, ViralcoronavirusCOVID-19near-infrared lightphotodynamic inactivationphotodynamic therapyphotosensitizerSARSSARS-CoV-2THPTS

Identifiers

PMID35746772
PMCPMC9229166

What Socratic 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 Socratic graph.