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DOI: 10.1055/s-0042-1746910
Immunohistochemical investigation of activated macrophages markers in middle ear cholesteatoma
Introduction
The pathogenesis of cholesteatoma is characterized by bone destruction of the middle ear, inner ear and skull base. The only treatment for cholesteatoma is currently the surgical removal. Although various infiltrating inflammatory and immune cells are involved in the pathogenesis of cholesteatoma, a leading role is played by macrophages. The activation of the macrophages by various stimuli leads to their polarization into the classically activated (M1) or alternatively activated (M2) phenotype. The distinct involvement of the different activation phenotypes of macrophages has been demonstrated in various inflammatory diseases. This observation implies that the investigation of the various macrophage profiles of cholesteatoma can be of therapeutic significance.
Material and Methods
The macrophages in cholesteatoma specimens were immunohistochemically characterized by an antibody combination of an M1 macrophage marker (CD80), an M2 macrophage marker (CD163) and a pan-macrophage marker (CD68). The immunohistochemical findings were correlated with the clinical presentation.
Results
M2 macrophages were more abundant than M1 macrophages in the perimatrix of the cholesteatome specimens. The relative ratio of M1 to M2 macrophages in the cholesteatoma specimens correlated with the extent of preoperative ossicular erosion.
Conclusion
The investigation of the polarization and functions of macrophages in various clinical presentations of cholesteatoma is of great interest in order to prevent the associated destructive inflammation and bone erosion. It is hoped that the results will contribute to the development of pharmaceutical treatment approaches and therefore to the expansion of the range of therapies of cholesteatoma.
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Conflict of Interest
The author declares that there is no conflict of interest.
Publication History
Article published online:
24 May 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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