Evidence map›Paper›PMID 40059759›Full record

ArticleEmerging microbes & infections2025

Evidence of Mpox clade IIb infection in primary human alveolar epithelium.

Thanaphon Namporn, Suwimon Manopwisedjaroen, Montien Ngodngamthaweesuk, Ekawat Pasomsub, Natnicha Jiravejchakul, Rattatammanoon Saengfak, Marea Jikka Nealiga, Arunsajee Sea-Be, Aalok Basu, Parichart Naruphontjirakul and 4 more

Abstract read
In one paragraph

Article in Emerging microbes & infections, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. 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.

Thanaphon NampornDivision of Pharmaceutical Technology, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Suwimon ManopwisedjaroenDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Montien NgodngamthaweesukCardioThoracic Surgery Unit, Department of Surgery, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Ekawat PasomsubVirology Unit, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Natnicha JiravejchakulDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Rattatammanoon SaengfakDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Marea Jikka NealigaDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Arunsajee Sea-BeDivision of Pharmaceutical Technology, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Aalok BasuDivision of Pharmaceutical Technology, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Parichart NaruphontjirakulBiological Engineering Program, Faculty of Engineering, King Mongkut's University of Technology Thonburi, Bangkok, Thailand.
Suradej HongengDepartment of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Teresa D TetleyLung Cell Biology, Section of Airways Disease, National Heart & Lung Institute, Imperial College London, London, UK.
Arunee ThitithanyanontDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Pakatip RuenraroengsakDivision of Pharmaceutical Technology, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monkeypox virus (Mpox) has been recognized for causing distinct skin lesions and is primarily transmitted through skin and sexual contact. To date, the transmissibility and pathogenesis of the Mpox virus in distal human lung has never been completely explored. Here the transmission pathways and Mpox tropism on patient-derived air-liquid epithelium (ALE) model fabricated using isolated primary human alveolar epithelial cells (hAECs) were investigated. hAECs were cultured and exposed to the Mpox virus clade IIb isolated from the patient. DNA, proteins, and the tropism were elucidated using polymerase chain reaction (PCR), Western blot, and high-content fluorescent imaging. Transmission electron microscopy (TEM) was employed to systematically observe the cellular distribution of viral particles. Viral titres were determined by TCID

Indexed as

Alveolar Epithelial CellsMpox, MonkeypoxPulmonary AlveoliCells, CulturedHumansMonkeypox virusViral Tropismair-liquid interfacealveolar epithelial cellslung modelmonkeypox virusMpoxOrthopoxviruspathogenesis

Identifiers

PMID40059759
PMCPMC11938317

What OpenQuestion holds

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LicenceCC BY
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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.