Evidence map›Paper›PMID 39527317›Full record

ArticleMedical microbiology and immunology2024

MPXV infection impairs IFN response but is partially sensitive to IFN-γ antiviral effect.

Licia Bordi, Alessandra D'Auria, Federica Frasca, Valentina Mazzotta, Paola Mazzetti, Matteo Fracella, Gabriella d'Ettorre, Guido Antonelli, Mauro Pistello, Andrea Antinori and 4 more

Abstract read
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Article in Medical microbiology and immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Inflammatory factors collaboratively linkFrontiers in immunology · 2025
    Review
  5. 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

14 authors.

Licia Bordi *Laboratory of Virology, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Rome, Italy.
Alessandra D'Auria *Department of Molecular Medicine, Laboratory of Virology, Sapienza University of Rome, Rome, Italy.
Federica FrascaDepartment of Molecular Medicine, Laboratory of Virology, Sapienza University of Rome, Rome, Italy.
Valentina MazzottaClinical Department, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Rome, Italy.
Paola MazzettiDepartment of Translational Research, Virology Section and Retrovirus Centre, University of Pisa, Pisa, Italy.
Matteo FracellaDepartment of Molecular Medicine, Laboratory of Virology, Sapienza University of Rome, Rome, Italy.
Gabriella d'EttorreDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Guido AntonelliDepartment of Molecular Medicine, Laboratory of Virology, Sapienza University of Rome, Rome, Italy.
Mauro PistelloDepartment of Translational Research, Virology Section and Retrovirus Centre, University of Pisa, Pisa, Italy.
Andrea AntinoriClinical Department, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Rome, Italy.
Raphael P ViscidiDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Fabrizio MaggiLaboratory of Virology, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Rome, Italy.
Eleonora Lalle *Laboratory of Virology, National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Rome, Italy.
Carolina Scagnolari *Department of Molecular Medicine, Laboratory of Virology, Sapienza University of Rome, Rome, Italy. carolina.scagnolari@uniroma1.it.

Funding

Next Generation EU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases (Project n. PE00000007, INF-ACT) PE00000007
6 · The paper itself

Abstract

The recent outbreak of monkeypox virus (MPXV) has caused global concern. How the virus evades the interferon (IFN) response is still poorly understood. We analyzed type I/II IFN (IFN-I/II) expression in clinical samples from MPXV-infected patients and measured IFN-I kinetics in MPXV-infected cells. We also evaluated the anti-MPXV activity of IFN-I/II in A549, HeLa and Vero-E6 cell lines. IFN-I/II mRNA expression was detected in skin lesions, anal swabs, nasopharyngeal samples and peripheral blood mononuclear cells (PBMC), with the highest levels in skin lesions (p < 0.05). High MPXV DNA levels in clinical samples were associated with increased IFN-I levels. In vitro, MPXV infection induced a peak of IFN-I between 48 and 72 h post-infection (p < 0.01). Pre-treatment of the A549, HeLa and Vero-E6 cells with high concentrations (≥ 100,000 International Unit, IU/ml) of IFN-α and IFN-ω did not inhibit or had little effect on MPXV replication, while IFN-β moderately reduced MPXV replication by 2.7-1.5 log

Indexed as

Interferon-gammaMonkeypox virusAnimalsAntiviral AgentsChlorocebus aethiopsHeLa CellsHumansInterferonsLeukocytes, MononuclearMpox, MonkeypoxVero CellsVirus ReplicationAntiviral AgentsInterferon-gammaInterferonsIDOIFN-γInnate immunityISGMonkeypox virusType I IFN

Identifiers

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Registered trials

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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.