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Published on: October 12, 2018
Immunological Microenvironment Diversity in Homogeneous and Non-Homogeneous Oral Leukoplakia
Ingrīda Čēma1,2, Regīna Kleina3, Madara Dzudzilo1,2
1Centre of Oral Medicine, Institute of Stomatology, Rīga Stradiņš University, Dzirciema Str. 20., LV-1007 Riga, Latvia.
International Journal of Molecular Sciences
|July 28, 2026
Summary
Oral leukoplakia (OL) risk assessment is improved by analyzing immune cell infiltration. Non-homogeneous OL with dysplasia shows increased T and B lymphocytes, aiding malignancy prediction.
Area of Science:
- Oral pathology
- Immunohistochemistry
- Cancer research
Background:
- Oral leukoplakia (OL) is a potentially malignant disorder with variable malignant transformation rates (7.2–9.5%).
- Understanding immune cell roles in OL progression is crucial for risk stratification.
Purpose of the Study:
- To investigate immune cell differences in homogeneous versus non-homogeneous OL.
- To correlate immune cell infiltration with dysplasia grades and malignancy risk.
Main Methods:
- Semi-quantitative assessment of T lymphocytes (CD3+), B lymphocytes (CD20+), macrophages (CD68+), plasma cells (CD138+), and CD9+ cells in 50 OL cases.
- Manual counting by two morphologists using a 4-point scale.
Main Results:
- Dysplastic OL, both homogeneous and non-homogeneous, showed higher CD138+ and CD68+ cell proportions.
- Non-homogeneous OL with dysplasia exhibited increased CD3+ and CD20+ lymphocyte infiltration.
- A positive correlation was found between CD9+ cells and epithelial labeling in OL of varying thickness.
- CD138 and CD9 expression suggests epithelial-mesenchymal interactions, with opposing patterns in epithelial vs. immune cells.
Conclusions:
- Evaluating CD3, CD20, CD9, CD138, and CD68 expression enhances malignancy risk assessment in dysplastic OL.
- Non-homogeneous OL with dysplasia presents distinct immune cell profiles, particularly increased T and B lymphocytes.
- Immune cell profiling offers a valuable tool for predicting OL malignant potential.
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