# Characterization of immune cells in periodontitis using a new histological immunologic gingival (IG) score

**Authors:** Emilie Hascoët, Frédéric Blanchard, Marie-Astrid Boutet, Maeva Dutilleul, Jérôme Guicheux, Philippe Lesclous, Alexandra Cloitre

PMC · DOI: 10.1038/s41598-025-25014-3 · Scientific Reports · 2026-01-16

## TL;DR

A new IG score was developed to characterize immune cells in periodontitis using immunohistochemistry, helping distinguish healthy and diseased tissue.

## Contribution

The study introduces a novel semi-quantitative IG score for immune cell characterization in periodontitis.

## Key findings

- The IG score was higher in periodontitis patients compared to healthy controls.
- A cut-off score of 4 out of 15 effectively discriminates between healthy and diseased tissue with over 90% specificity and sensitivity.

## Abstract

Periodontitis is a prevalent chronic inflammatory disease due to the host response to dysbiotic biofilm. Immunohistochemistry is often used for a better and more functional tissue characterization. The main objective of this study was to create a semi-quantitative Immunologic Gingival (IG) score for characterizing immune cells in periodontitis based on five immunohistochemical stainings. The study included 11 healthy controls and 11 periodontitis patients. To determine the IG score, an atlas was drawn up with five immunohistochemical stainings (CD138, CD3, CD20, CD68, CD66b). The mean IG score was higher for periodontitis patients than for healthy controls. For each marker of the IG score, a positive correlation was found between the semi-quantitative score and the respective percentage of positive cells. An IG score of 4 out of 15 was the best cut-off for discrimination between healthy controls and periodontitis patients, with a specificity and a sensitivity exceeding 90%. The IG score provides standardized information on the immune cell signature in gingival samples from patients with periodontitis. This score could be applied in translational research but also in clinical practice, particularly for the development of personalized therapies for patients with recurrent periodontitis.

The online version contains supplementary material available at 10.1038/s41598-025-25014-3.

## Linked entities

- **Proteins:** SDC1 (syndecan 1), cd.3 (Cd.3 conserved hypothetical protein), MS4A1 (membrane spanning 4-domains A1), CD68 (CD68 molecule), CEACAM8 (CEA cell adhesion molecule 8)
- **Diseases:** periodontitis (MONDO:0005076)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, SDC1 (syndecan 1) [NCBI Gene 6382] {aka CD138, SDC, SYND1, syndecan}, CEACAM8 (CEA cell adhesion molecule 8) [NCBI Gene 1088] {aka CD66b, CD67, CGM6, NCA-95}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** Periodontitis (MESH:D010518), inflammatory disease (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12816066/full.md

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Source: https://tomesphere.com/paper/PMC12816066