Evidence map›Paper›PMID 39310226›Full record

ArticleFrontiers in cell and developmental biology2024

Tlr7 drives sex- and tissue-dependent effects in Sjögren's disease.

Achamaporn Punnanitinont, Sheta Biswas, Eileen M Kasperek, Jason Osinski, Chengsong Zhu, Jeffrey C Miecznikowski, Rose-Anne Romano, Jill M Kramer

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Molecular Insights into Oral Manifestations in Sjögren's Disease.International journal of molecular sciences · 2026
    Review
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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

8 authors.

Achamaporn PunnanitinontDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Sheta BiswasDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Eileen M KasperekDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Jason OsinskiDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Chengsong ZhuDepartment of Immunology, Microarray and Immune Phenotyping Core Facility, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Jeffrey C MiecznikowskiDepartment of Biostatistics, School of Public Health and Health Professions, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Rose-Anne RomanoDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
Jill M KramerDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.

Funding

University of Buffalo Clinical and Translational Science Institute - Supplement SchulyerUL1TR001412 · NCATS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MURPHY, TIMOTHY F · 2015 to 2024
$33.8M
Advanced Training in Oral BiologyT32DE023526 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Stefan Hans-Klaus Ruhl · 2013 to 2026
$3.7M
Analysis of MyD88-mediated immune activation in Sjogrens syndrome pathogenesisR01DE029472 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Jill Marie Kramer · 2020 to 2026
$2.7M
Spinning disk confocal microscopeS10OD025204 · OD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI KAY, JASON G · 2019 to 2019
$488k
Role of TLR7-mediated B cell activation in primary Sjogren’s syndromeF31DE032884 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI PUNNANITINONT, ACHAMAPORN · 2023 to 2024
$59k
NCATS NIH HHS UL1 TR001412NIDCR NIH HHS F31 DE032884NIDCR NIH HHS R01 DE029472NIDCR NIH HHS T32 DE023526NIH HHS S10 OD025204
6 · The paper itself

Abstract

Primary Sjögren's disease (pSD) is a systemic autoimmune disease that has the strongest female predilection of all autoimmune diseases. The underlying mechanisms that govern this sexual dimorphism, however, remain poorly understood. We hypothesized that pSD females would exhibit more robust disease as compared to males, and that Tlr7 controls distinct disease manifestations in males and females. Using a well-established pSD mouse model, we harvested exocrine glands, and pulmonary and renal tissue from males and females and quantified the inflammation present. We then collected salivary glands, spleens, and cervical lymph nodes and performed flow cytometry to assess immune populations implicated in disease. We also harvested sera to examine total and autoreactive antibodies. Our data revealed that pSD mice displayed sex-biased disease, as pSD females showed decreased dacryoadenitis, but increased nephritis as compared to males. Moreover, females exhibited increased proportions of germinal center B cells and CD4

Indexed as

age-associated B cells (ABC)autoantibodiesNOD.B10salivasialadenitis

Identifiers

PMID39310226
PMCPMC11413591

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.