Evidence map›Paper›PMID 41688543›Full record

ArticleCommunications biology2026

Pathological characteristics of SARS-CoV-2 variants and immune responses induced in a COVID-19 macaque model.

Emiko Urano, Tomotaka Okamura, Mahoko Higuchi, Mugi Furukawa, Kayoko Ueda, Satoshi Nagata, Haruhiko Kamada, Yasuhiro Yasutomi

Abstract read
In one paragraph

Article in Communications biology, 2026. 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

8 authors.

Emiko UranoLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Tomotaka OkamuraLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Mahoko HiguchiLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Mugi FurukawaLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Kayoko UedaLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Satoshi NagataLaboratory of Antibody Design, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, Japan.ORCID http://orcid.org/0000-0001-9156-5215
Haruhiko KamadaCenter for Drug Design Research, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, Japan.
Yasuhiro YasutomiLaboratory of Immunoregulation and Vaccine Research, Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan. yasutomi@nibn.go.jp.ORCID http://orcid.org/0000-0001-8252-1448

Funding

Japan Agency for Medical Research and Development (AMED) JP20fk0108414Japan Agency for Medical Research and Development (AMED) JP21fk0108582Japan Agency for Medical Research and Development (AMED) JP223fa627005Japan Agency for Medical Research and Development (AMED) JP223fa627007Japan Agency for Medical Research and Development (AMED) JP223fa727002MEXT | Japan Science and Technology Agency (JST) JPMJPF2017MEXT | Japan Society for the Promotion of Science (JSPS) 21K19395
6 · The paper itself

Abstract

Although recent studies have suggested that the Omicron strain is less severe, the prevalence of long Omicron variants and their subvariant waves continues today. Here, we analyze the pathological characteristics of SARS-CoV-2 variants in cynomolgus macaques. Prolonged re-challenge analysis results in the establishment of re-infection in some macaques with both the same strain and different strains. Omicron infection shows low pathogenicity; however, all macaques that developed pneumonia were inoculated with Omicron strains at the second inoculation. Interestingly, antibodies against the Wuhan, Alpha, and Delta strains are strongly induced regardless of the strain, but antibodies against Omicron strains are not. Moreover, despite the re-infection strain, antibody levels against the Wuhan strain are highest, suggesting original antigenic sin. In addition, Omicron infection induces weaker antigen-specific T-cell responses. These results indicate that immune responses to viral infection differ between the variants, and these differences could inform vaccine development strategies.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, ViralDisease Models, AnimalMacaca fascicularisT-LymphocytesAntibodies, Viral

Identifiers

PMID41688543
PMCPMC13013701

What OpenQuestion holds

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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.