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Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study
BACKGROUND: Macrophages are important cells for the innate immunity. Circulating monocytes are attracted to tissues by chemotactic factors and become macrophages under the influence of their microenvironment. Several studies suggested that local and systemic upregulation of fibrogenic cytokines and...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804656/ https://www.ncbi.nlm.nih.gov/pubmed/27057383 http://dx.doi.org/10.4103/2141-9248.177983 |
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author | Pereira, T Naik, S Tamgadge, A |
author_facet | Pereira, T Naik, S Tamgadge, A |
author_sort | Pereira, T |
collection | PubMed |
description | BACKGROUND: Macrophages are important cells for the innate immunity. Circulating monocytes are attracted to tissues by chemotactic factors and become macrophages under the influence of their microenvironment. Several studies suggested that local and systemic upregulation of fibrogenic cytokines and downregulation of antifibrotic cytokine are central to the pathogenesis of oral submucous fibrosis (OSMF). Currently, there have been no attempts made to elucidate the presence and role of macrophages in OSMF. AIM: Our aim was to study the expression of CD68 in OSMF patients and to investigate the possible correlation of macrophages using CD68 in various histopathological grades of OSMF. SUBJECTS AND METHODS: A prospective case–control study which included 40 patients was conducted after obtaining informed consent and Ethical Committee clearance. Ten cases were normal control and thirty cases had OSMF. Biopsy was performed and a quantitative study of macrophages was done using CD68 antigen and was immunohistochemically localized. Statistical analysis was carried out using the Statistical Package for Social Sciences (SPSS) 17.0 version (SPSS Inc., Chicago, IL, USA). RESULTS: OSMF was observed in male patients of a younger age group. The macrophage number in the patients of intermediate and advanced stage of OSMF was higher than that of the controls which was statistically significant (P < 0.05). CONCLUSION: The findings of this study suggest that CD68 plays a vital role in the pathogenesis of OSMF and can be regarded as a useful marker for assessing the progress of the disease. |
format | Online Article Text |
id | pubmed-4804656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48046562016-04-07 Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study Pereira, T Naik, S Tamgadge, A Ann Med Health Sci Res Original Article BACKGROUND: Macrophages are important cells for the innate immunity. Circulating monocytes are attracted to tissues by chemotactic factors and become macrophages under the influence of their microenvironment. Several studies suggested that local and systemic upregulation of fibrogenic cytokines and downregulation of antifibrotic cytokine are central to the pathogenesis of oral submucous fibrosis (OSMF). Currently, there have been no attempts made to elucidate the presence and role of macrophages in OSMF. AIM: Our aim was to study the expression of CD68 in OSMF patients and to investigate the possible correlation of macrophages using CD68 in various histopathological grades of OSMF. SUBJECTS AND METHODS: A prospective case–control study which included 40 patients was conducted after obtaining informed consent and Ethical Committee clearance. Ten cases were normal control and thirty cases had OSMF. Biopsy was performed and a quantitative study of macrophages was done using CD68 antigen and was immunohistochemically localized. Statistical analysis was carried out using the Statistical Package for Social Sciences (SPSS) 17.0 version (SPSS Inc., Chicago, IL, USA). RESULTS: OSMF was observed in male patients of a younger age group. The macrophage number in the patients of intermediate and advanced stage of OSMF was higher than that of the controls which was statistically significant (P < 0.05). CONCLUSION: The findings of this study suggest that CD68 plays a vital role in the pathogenesis of OSMF and can be regarded as a useful marker for assessing the progress of the disease. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4804656/ /pubmed/27057383 http://dx.doi.org/10.4103/2141-9248.177983 Text en Copyright: © Annals of Medical and Health Sciences Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Pereira, T Naik, S Tamgadge, A Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title | Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title_full | Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title_fullStr | Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title_full_unstemmed | Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title_short | Quantitative Evaluation of Macrophage Expression Using CD68 in Oral Submucous Fibrosis: An Immunohistochemical Study |
title_sort | quantitative evaluation of macrophage expression using cd68 in oral submucous fibrosis: an immunohistochemical study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804656/ https://www.ncbi.nlm.nih.gov/pubmed/27057383 http://dx.doi.org/10.4103/2141-9248.177983 |
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