Evidence map›Paper›PMID 40983612›Full record

ArticleNature communications2025

Comparative single-cell and spatial profiling of anti-SSA-positive and anti-centromere-positive Sjögren's disease reveals common and distinct immune activation and fibroblast-mediated inflammation.

Jun Inamo, Masaru Takeshita, Katsuya Suzuki, Kazuyuki Tsunoda, Satoshi Usuda, Junko Kuramoto, Jonathan Moody, Chung-Chau Hon, Yoshinari Ando, Takashi Sasaki and 6 more

Abstract readComparative Study
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Agentic AI for Spatial Omics.Immunology and cell biology · 2026
    Review
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  5. Article
  6. Article
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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

16 authors.

Jun Inamo *Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan. juninamo@keio.jp.ORCID http://orcid.org/0000-0002-9927-7936
Masaru Takeshita *Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan. takeshita.a5@keio.jp.ORCID http://orcid.org/0000-0002-3281-6595
Katsuya SuzukiDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Kazuyuki TsunodaDepartment of Dentistry and Oral Surgery, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Satoshi UsudaDepartment of Dentistry and Oral Surgery, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Junko KuramotoDepartment of Pathology, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Jonathan MoodyLaboratory for Regulatory Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.ORCID http://orcid.org/0000-0001-9261-711X
Chung-Chau HonLaboratory for Regulatory Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.ORCID http://orcid.org/0000-0002-3741-7577
Yoshinari AndoLaboratory for Regulatory Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.ORCID http://orcid.org/0000-0002-8128-6201
Takashi SasakiCenter for Supercentenarian Medical Research, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6275-046X
Kazutoshi YoshitakeLaboratory of Aquatic Molecular Biology and Biotechnology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Susumu MitsuyamaLaboratory of Aquatic Molecular Biology and Biotechnology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID http://orcid.org/0009-0002-5965-9363
Shuichi AsakawaLaboratory of Aquatic Molecular Biology and Biotechnology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Yae KanaiDepartment of Pathology, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Tsutomu TakeuchiDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Yuko KanekoDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP20H03720MEXT | Japan Society for the Promotion of Science (JSPS) JP20K17430MEXT | Japan Society for the Promotion of Science (JSPS) JP21J00596MEXT | Japan Society for the Promotion of Science (JSPS) JP22K08528
6 · The paper itself

Abstract

Sjögren's disease (SjD) is an autoimmune disease that causes salivary gland dysfunction due to immune-mediated destruction. While autoantibodies such as anti-SSA and anti-centromere (CENT) are associated with distinct clinical manifestations, the molecular features remain to be elucidated. In this study, we apply multi-modal single-cell technologies: single-cell RNA sequencing, T cell and B cell receptor sequencing and spatial transcriptomics to salivary gland lesions, aiming to elucidate common and unique cellular and transcriptional signatures linked to different autoantibody profiles. Our analysis demonstrates that GZMB

Indexed as

Antibodies, AntinuclearFibroblastsSjogren's SyndromeAdultAutoantibodiesB-LymphocytesCD8-Positive T-LymphocytesCytokinesFemaleHumansInflammationMaleMiddle AgedSalivary GlandsSignal TransductionSingle-Cell AnalysisAntibodies, AntinuclearAutoantibodiesCytokines

Identifiers

PMID40983612
PMCPMC12454658

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.