Evidence map›Paper›PMID 41988349›Full record

ReviewFrontiers in dental medicine2026

Immune suppression, HLA-risk and potential future immune based targets of oral leukoplakia progression.

Mehar Soni, Bryce DeSantis, Alessandro Villa, Malek Kamoun, James Gates

Abstract readReview
In one paragraph

Review in Frontiers in dental medicine, 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

5 authors.

Mehar SoniSchool of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Bryce DeSantisSchool of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Alessandro VillaOral Medicine and Oral Oncology, Miami Cancer Institute, Miami, FL, United States.
Malek KamounPathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, United States.
James GatesDepartment of Oral and Maxillofacial Surgery, Penn Dental Medicine, University of Pennsylvania and Hospital of the University of Pennsylvania, Philadelphia, PA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Oral leukoplakia (OL) is the most common oral potentially malignant disorder and carries a non-trivial risk of malignant transformation. Biomarkers are sought to aid in identifying lesions with high risk for malignant transformation, yet none are currently validated. Recent success of immune based therapies in head and neck oncology highlights immune involvement in the progression of these diseases. The differential expression of classical and non-classical HLA molecules in oral leukoplakia are thought to contribute to their malignant transformation. To better evaluate the role HLA plays in oral pre-malignant lesions, a scoping review was performed. Methods: A scoping review was conducted in accordance with the PRISMA guidelines across PubMed, EMBASE, and Web of Science. 293 studies were reviewed from 1989 to 2025. Results: 15 studies were screened by title, then 5 original research abstracts were included. Samples studied ranged from Conclusion: The upregulation of non-classical HLA molecules, particularly HLA-G, HLA-E, and circHLA-C in oral leukoplakia, suggests an immunologic shift, potentially facilitating tumor immune evasion in oral leukoplakic lesions. HLA expression may serve as a potential biomarker for identifying pre-malignant oral lesions at increased risk of malignant transformation. Also, circHLA-C may provide a target for therapeutic intervention in high-risk oral premalignant lesions.

Indexed as

biomarkersdysplasiahuman leukocyte antigenleukoplakiaoncology

Identifiers

PMID41988349
PMCPMC13076277

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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.