Evidence map›Paper›PMID 40546085›Full record

ArticleThe Laryngoscope2025

Toll Like Receptors in the Larynx: Implications for Laryngeal Immunology.

Madhu Gowda, Anumitha Venkatraman, Alexandra Mechler-Hickson, Vlasta Lungova, Susan L Thibeault

Abstract read
In one paragraph

Article in The Laryngoscope, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

5 authors.

Madhu GowdaDivision of Otolaryngology Head and Neck Surgery, University of Wisconsin Madison, Madison, Wisconsin, USA.
Anumitha VenkatramanDivision of Otolaryngology Head and Neck Surgery, University of Wisconsin Madison, Madison, Wisconsin, USA.ORCID 0000-0003-4341-9701
Alexandra Mechler-HicksonDivision of Otolaryngology Head and Neck Surgery, University of Wisconsin Madison, Madison, Wisconsin, USA.
Vlasta LungovaDivision of Otolaryngology Head and Neck Surgery, University of Wisconsin Madison, Madison, Wisconsin, USA.
Susan L ThibeaultDivision of Otolaryngology Head and Neck Surgery, University of Wisconsin Madison, Madison, Wisconsin, USA.ORCID 0000-0002-9046-4356

Funding

Engineering the Vocal Fold MucosaR01DC004336 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI Susan Lynn Thibeault · 2000 to 2026
$14.6M
Mechanisms of innate immune-microbial interactions in vocal fold InflammationR01DC012773 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI THIBEAULT, SUSAN LYNN · 2013 to 2022
$4.5M
NIDCD NIH HHS DC012773NIDCD NIH HHS DC4336NIDCD NIH HHS R01 DC004336NIDCD NIH HHS R01 DC012773NIDCD NIH HHS T3209401
6 · The paper itself

Abstract

rationaleAlthough optimal epithelial barrier function is essential to laryngeal health and disease, there is a surprising paucity of literature on the underlying immunological mechanisms in laryngeal epithelia. Toll like receptors (TLR) are a class of pattern-recognition receptor (PRR) proteins that are essential for regulating the innate and adaptive immune response in mucosal epithelia. Identifying the presence of TLR receptors in laryngeal epithelia and delineating their role in laryngeal inflammation will contribute to our understanding of innate and adaptive immune responses in the vocal fold mucosa.

objective(1) To delineate TLR expression in human and murine vocal fold epithelium, (2) to elucidate the mechanisms of TLR-dependent inflammation in primary human vocal fold epithelial cell cultures.

methodsIn our first experiment, we histologically characterized normal TLR 1-9 expression in human and murine laryngeal epithelium. In our second experiment, we quantified transcript expression of TLR 1-9 and IL8 in primary human vocal fold epithelial cell cultures, incubated with and without LPS.

resultsTLR were identified in the murine and human vocal fold epithelium with slight differences in localization from true to false vocal folds in humans. In primary human vocal fold epithelial cell cultures, there was a significant increase in relative gene expression at 24 h for TLRs 2, 3, and 6, as well as IL8 with LPS stimulation.

conclusionsThis is the first study to identify the presence of TLR receptors in the human and murine vocal fold epithelium. These data lay the groundwork for delineating the role of TLR in the laryngeal immune response in both healthy and pathological states. LEVEL OF EVIDENCE: NA.

Indexed as

Laryngeal MucosaLarynxToll-Like ReceptorsVocal CordsAnimalsCells, CulturedEpithelial CellsHumansImmunity, InnateMiceMice, Inbred C57BLToll-Like Receptorslarynxtoll like receptorsvocal fold epithelium

Identifiers

PMID40546085
PMCPMC12475540

What OpenQuestion holds

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LicenceCC BY-NC
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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.