Do Langerhans cells behave similarly in elderly and younger patients with chronic periodontitis?
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Updated: Jul 18, 2026

Isolation, Processing and Analysis of Murine Gingival Cells
Published on: July 2, 2013
Agnès Bodineau1, Bernard Coulomb, Marysette Folliguet
1Laboratoire sur la Réparation et les Remodelages Oro-Faciaux (EA2496), Faculté de Chirurgie Dentaire, Université René Descartes - Paris 5, 1 rue Maurice Arnoux, 92120 Montrouge, France.
Objective:
The purpose of this study was to compare the number, the distribution and the expression of markers of maturation of Langerhans cells (LC) in elderly and younger patients with chronic periodontitis in order to evidence the effect of aging on LC in inflammatory gingival tissue.
Methods:
Gingival tissue specimens presenting chronic periodontitis from 8 elderly patients aged >75 (group E) and from 8 younger patients aged 50-60 (considered as controls, group C) were used for immunohistochemistry with monoclonal antibodies against CD45RB (leucocytes), CD1a (LC), markers of LC maturation (DC-LAMP, CD83) and number of immunolabelled cell subsets was evaluated using image analysis.
Results:
The difference in the number of CD45RB+ leucocytes in the upper connective tissue between groups was not significant. In group E, the number of CD1a+ LC was significantly decreased (P<0.002) in the epithelium and significantly increased (P<0.0004) in the upper connective tissue. Furthermore, in group E, intraepithelial CD1a+ LC are more often observed in the upper epithelium and their dendritic processes were shorter and less numerous. Concerning the expression of markers of maturation, the numbers of intraepithelial DC-LAMP+ cells and CD83+ cells were significantly increased (P<0.0007 and P<0.02, respectively) in group E.
Conclusion:
During chronic periodontitis in elderly patients, the decrease in the number of intraepithelial LC and the alteration of dendritic processes could be balanced by a cellular distribution often observed in the upper epithelium associated with changes in cell maturation in response to bacterial elements.
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