Evidence map›Paper›PMID 39572887›Full record

ArticleMicrobiology and immunology2025

A Mouse Model of Ovalbumin-Induced Airway Allergy Exhibits Altered Localization of SARS-CoV-2-Susceptible Cells in the Lungs, Which Reflects Omicron BA.5 Infection Dynamics, Viral Mutations, and Immunopathology.

Takao Iketani, Kaya Miyazaki, Naoko Iwata-Yoshikawa, Yusuke Sakai, Nozomi Shiwa-Sudo, Seiya Ozono, Hideki Asanuma, Hideki Hasegawa, Tadaki Suzuki, Noriyo Nagata

Abstract read
In one paragraph

Article in Microbiology and immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Takao IketaniDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Kaya MiyazakiResearch Center for Influenza and Respiratory Viruses, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Naoko Iwata-YoshikawaDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.ORCID http://orcid.org/0000-0001-7818-686X
Yusuke SakaiDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Nozomi Shiwa-SudoDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.ORCID http://orcid.org/0000-0002-4135-322X
Seiya OzonoDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Hideki AsanumaDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Hideki HasegawaResearch Center for Influenza and Respiratory Viruses, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Tadaki SuzukiDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3820-9542
Noriyo NagataDepartment of Pathology, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9147-1438

Funding

Ministry of Education, Culture, Sports, Science and Technology.This study was supported by the Japan Agency for Medical Research and Development
6 · The paper itself

Abstract

Asthma, an allergic disease of the airways, is a risk factor for severity of common respiratory viral infections; however, the relationship between asthma and severity in COVID-19 remains unclear. Here, we examined the effects of SARS-CoV-2 (Omicron BA.5 strain) infection in a mouse model of airway allergy. First, stimulation of allergic mice with OVA resulted in the appearance of ACE2-negative mucus-secreting goblet cells in the bronchiolar region, and an increase in the number of ACE2-expressing cells in the alveoli. As a result, ACE2-expressing cells, which are susceptible to SARS-CoV-2, were limited to the distal portion of the bronchioles while they increased in the alveolar area. After viral infection, the peak infectious viral load in the OVA group was 100-fold lower than that in the phosphate buffered saline (PBS) group; however, clearance of viral RNA from the upper/lower airways was delayed. There were notable differences in acquisition of nsp5 and nsp6 mutations by the Omicron BA.5 strain recovered from BALF samples obtained from the OVA and PBS groups. Immune responses associated with viral clearance were essentially the same, but expression of granulocyte-associated chemokines was higher, M2 macrophage responses were predominant, and the higher spike-specific IgG1/IgG2a ratio in the OVA group post-infection. Infection localized in the alveolar region earlier in the OVA group, resulting in more severe alveolar damage than in the PBS group. These data suggest a Th2-shifted immune background and altered localization of SARS-CoV-2 susceptible cells in mice with OVA-induced airway allergy, which reflect Omicron BA.5 infection dynamics, viral mutations, and immunopathology.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19Disease Models, AnimalLungMutationOvalbuminSARS-CoV-2AnimalsAsthmaBronchoalveolar Lavage FluidFemaleGoblet CellsHumansMiceMice, Inbred BALB CViral LoadAce2 protein, mouseAngiotensin-Converting Enzyme 2OvalbuminACE2allergic murine modelimmunopathologyOmicronovalbuminSARS‐CoV‐2variants

Identifiers

PMID39572887
PMCPMC11701410

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.