Evidence map›Paper›PMID 42585251›Full record

ArticlePloS one2026

Eosinophil-associated intestinal immune responses following SARS-CoV-2 infection in K18-hACE2 mice.

Shun Tamaki, Rei Kawashima, Takayuki Uematsu, Fumitaka Kawakami, Motoki Imai, Yoshifumi Kurosaki, Toshihide Matsumoto, Shotaro Maehana, Yusuke Hara, Setsuko Sugawara and 5 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

15 authors.

Shun TamakiDepartment of Biochemistry, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Rei KawashimaDepartment of Biochemistry, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Takayuki UematsuLaboratory of Infection Immunology, Department of Infection Control and Immunology, O̅mura Satoshi Memorial Institute, Kitasato University, Minato-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3680-7231
Fumitaka KawakamiDepartment of Regulation Biochemistry, Kitasato University Graduate School of Medical Sciences, Sagamihara, Kanagawa, Japan.
Motoki ImaiRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Yoshifumi KurosakiDepartment of Regulation Biochemistry, Kitasato University Graduate School of Medical Sciences, Sagamihara, Kanagawa, Japan.
Toshihide MatsumotoRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Shotaro MaehanaRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Yusuke HaraDepartment of Biochemistry, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Setsuko SugawaraDepartment of Biochemistry, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Hiroki IzawaRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Takafumi IchikawaDepartment of Biochemistry, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Hidero KitasatoRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.
Hideaki HanakiInfection Control Research Center, Ōmura Satoshi Memorial Institute, Kitasato University, Minato-ku, Tokyo, Japan.
Makoto KuboRegenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara, Kanagawa, Japan.ORCID https://orcid.org/0000-0001-8264-1343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is frequently associated with gastrointestinal manifestations; however, intestinal immune responses following SARS-CoV-2 infection remain incompletely understood. This study aimed to characterize eosinophil-associated intestinal immune responses in SARS-CoV-2-infected K18-hACE2 transgenic mice.

methodsSmall intestinal tissues from infected mice were analyzed using cytokine and chemokine PCR arrays, qRT-PCR, immunohistochemistry, and histological analyses.

resultsSARS-CoV-2 infection was associated with marked upregulation of Il5 mRNA in small intestinal tissues, along with increased expression of eosinophil-related cytokines and chemokines, including Ccl24 and Ccl11. Immunohistochemical analyses showed eosinophil accumulation in the lamina propria, accompanied by increased signals for eosinophil-associated granule proteins, including major basic protein and eosinophil peroxidase. Additional qRT-PCR analyses showed increased expression of Prg2 and Epx, further supporting eosinophil granule protein-associated responses. Charcot-Leyden crystals and increased Galectin-10 expression were also observed. Temporal analyses showed an acute Il5/Ccl24-related response followed by delayed Ccl11 upregulation during later stages.

conclusionsThese findings indicate that SARS-CoV-2 infection is associated with eosinophil-associated intestinal immune responses in K18-hACE2 mice. Although eosinophil activation or intestinal allergy was not directly demonstrated, this study supports virus-associated eosinophil-related intestinal responses as a possible framework for understanding allergy-like intestinal immune alterations during SARS-CoV-2 infection.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19EosinophilsIntestinesIntestine, SmallSARS-CoV-2AnimalsChemokine CCL11Chemokine CCL24CytokinesIntestinal MucosaMiceMice, TransgenicAce2 protein, mouseAngiotensin-Converting Enzyme 2Ccl11 protein, mouseCcl24 protein, mouseChemokine CCL11Chemokine CCL24Cytokines

Identifiers

PMID42585251
PMCPMC13465793

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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.