Evidence map›Paper›PMID 36591307›Full record

ArticleFrontiers in immunology2022

TLR7 agonism accelerates disease in a mouse model of primary Sjögren's syndrome and drives expansion of T-bet

Achamaporn Punnanitinont, Eileen M Kasperek, Jeremy Kiripolsky, Chengsong Zhu, Jeffrey C Miecznikowski, Jill M Kramer

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Molecular Insights into Oral Manifestations in Sjögren's Disease.International journal of molecular sciences · 2026
    Review
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  12. Tlr7 drives sex- and tissue-dependent effects in Sjögren's disease.Frontiers in cell and developmental biology · 2024
    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

6 authors at 2 institutions in 1 country.

Achamaporn PunnanitinontDepartment 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.
Jeremy KiripolskyDepartment 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 & 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.
Jill M KramerDepartment of Oral Biology, School of Dental Medicine, The University at Buffalo, State University of New York, Buffalo, NY, United States.
University at Buffalo, State University of New York · USThe University of Texas Southwestern Medical Center · US

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
NCATS NIH HHS UL1 TR001412NIDCR NIH HHS R01 DE029472NIDCR NIH HHS T32 DE023526
6 · The paper itself

Abstract

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterized by chronic inflammation of exocrine tissue, resulting in loss of tears and saliva. Patients also experience many extra-glandular disease manifestations. Treatment for pSS is palliative, and there are currently no treatments available that target disease etiology. Previous studies in our lab demonstrated that MyD88 is crucial for pSS pathogenesis in the NOD.B10Sn-

Indexed as

B-LymphocytesMyeloid Differentiation Factor 88Sjogren's SyndromeToll-Like Receptor 7Adjuvants, ImmunologicAnimalsFemaleImiquimodMiceMice, Inbred C57BLMice, Inbred NODAdjuvants, ImmunologicImiquimodMyeloid Differentiation Factor 88Toll-Like Receptor 7ABCage-associated B cellsautoantibodiesautoimmunityNOD.B10sialadenitis

Identifiers

PMID36591307
PMCPMC9799719
OpenAlexW4311511469

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.