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Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population

BACKGROUND: Localized aggressive periodontitis (LAP) patients exhibit abnormal neutrophil functions to a variety of environmental and host stimuli. The aim of the present study was to evaluate neutrophils chemotaxis, phagocytosis, microbicidal activity and superoxide generation in LAP patients of In...

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Autores principales: Bhansali, Rahul S., Yeltiwar, R. K., Bhat, K. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917201/
https://www.ncbi.nlm.nih.gov/pubmed/24554881
http://dx.doi.org/10.4103/0972-124X.124485
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author Bhansali, Rahul S.
Yeltiwar, R. K.
Bhat, K. G.
author_facet Bhansali, Rahul S.
Yeltiwar, R. K.
Bhat, K. G.
author_sort Bhansali, Rahul S.
collection PubMed
description BACKGROUND: Localized aggressive periodontitis (LAP) patients exhibit abnormal neutrophil functions to a variety of environmental and host stimuli. The aim of the present study was to evaluate neutrophils chemotaxis, phagocytosis, microbicidal activity and superoxide generation in LAP patients of Indian origin. MATERIALS AND METHODS: Eleven LAP patients and nine healthy subjects were included in the study. Neutrophil chemotaxis was evaluated against an alkali-soluble casein solution using Wilkinson's method. Phagocytosis and microbicidal activity assay were performed using Candida albicans as an indicator organism. Nitrobluetetrazolium (NBT) test was used to assess superoxide generation by neutrophils using E. coli endotoxin. RESULTS: The chemotactic activity and phagocytic and microbicidal activity were observed to be significantly reduced (P < 0.01) in LAP neutrophils. On the contrary, superoxide generation was observed to be significantly increased (P < 0.01) in LAP neutrophils compared with healthy individuals. CONCLUSION: The results of the present study suggest that neutrophil functions, namely chemotaxis, phagocytosis and microbicidal activity, are deficient LAP patients. However, superoxide generation was significantly increased when stimulated by endotoxins, which may explain the tissue damage seen in LAP. These abnormal neutrophil functions may predispose to increased susceptibility for LAP. Further large-scale studies are required in the Indian population to ascertain the cause-and-effect relationship of defective host factors and aggressive periodontitis and to develop treatment strategies for more predictable periodontal treatment outcome.
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spelling pubmed-39172012014-02-19 Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population Bhansali, Rahul S. Yeltiwar, R. K. Bhat, K. G. J Indian Soc Periodontol Original Article BACKGROUND: Localized aggressive periodontitis (LAP) patients exhibit abnormal neutrophil functions to a variety of environmental and host stimuli. The aim of the present study was to evaluate neutrophils chemotaxis, phagocytosis, microbicidal activity and superoxide generation in LAP patients of Indian origin. MATERIALS AND METHODS: Eleven LAP patients and nine healthy subjects were included in the study. Neutrophil chemotaxis was evaluated against an alkali-soluble casein solution using Wilkinson's method. Phagocytosis and microbicidal activity assay were performed using Candida albicans as an indicator organism. Nitrobluetetrazolium (NBT) test was used to assess superoxide generation by neutrophils using E. coli endotoxin. RESULTS: The chemotactic activity and phagocytic and microbicidal activity were observed to be significantly reduced (P < 0.01) in LAP neutrophils. On the contrary, superoxide generation was observed to be significantly increased (P < 0.01) in LAP neutrophils compared with healthy individuals. CONCLUSION: The results of the present study suggest that neutrophil functions, namely chemotaxis, phagocytosis and microbicidal activity, are deficient LAP patients. However, superoxide generation was significantly increased when stimulated by endotoxins, which may explain the tissue damage seen in LAP. These abnormal neutrophil functions may predispose to increased susceptibility for LAP. Further large-scale studies are required in the Indian population to ascertain the cause-and-effect relationship of defective host factors and aggressive periodontitis and to develop treatment strategies for more predictable periodontal treatment outcome. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3917201/ /pubmed/24554881 http://dx.doi.org/10.4103/0972-124X.124485 Text en Copyright: © Journal of Indian Society of Periodontology 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bhansali, Rahul S.
Yeltiwar, R. K.
Bhat, K. G.
Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title_full Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title_fullStr Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title_full_unstemmed Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title_short Assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the Indian population
title_sort assessment of peripheral neutrophil functions in patients with localized aggressive periodontitis in the indian population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917201/
https://www.ncbi.nlm.nih.gov/pubmed/24554881
http://dx.doi.org/10.4103/0972-124X.124485
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