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Browsing by Author "Andric, M. (20435687400)"

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    Herpesviruses viral loads and levels of proinflammatory cytokines in apical periodontitis
    (2018)
    Jakovljevic, A. (56396874600)
    ;
    Knezevic, A. (22034890600)
    ;
    Nikolic, N. (55324775800)
    ;
    Soldatovic, I. (35389846900)
    ;
    Jovanovic, T. (26642921700)
    ;
    Milasin, J. (6603015594)
    ;
    Andric, M. (20435687400)
    Objectives: This study aimed to analyse Epstein–Barr virus (EBV) and human cytomegalovirus (HCMV) viral loads in symptomatic and asymptomatic apical periodontitis lesions, to determine levels of TNF-α, IL-1β and IL-6 in these lesions and to investigate a possible correlation between herpesviral copy numbers and levels of proinflammatory cytokines. Materials and Methods: A total of 100 samples of apical periodontitis were subjected to HCMV and EBV copy numbers analysis by nested polymerase chain reaction (PCR) and TaqMan real-time PCR. The concentrations of TNF-α, IL-1β and IL-6 were determined by ELISA method. SPSS software was used for statistical analysis. Results: There were no significant differences in the occurrence of EBV and HCMV between symptomatic and asymptomatic periapical lesions (p =.686, p =.879, respectively). Only 12 of 74 EBV (16.2%) and four of 54 HCMV (13.5%) nested PCR-positive samples showed increased viral copy numbers above the limit of 125 copies/ml. There was no significant correlation between the levels of analysed proinflammatory cytokines and herpesviral copy numbers in our sample. Conclusion: The observed low viral loads point to a relatively rare occurrence of active EBV and HCMV infection in our sample. Latent herpesviral infection does not enhance the production of investigated proinflammatory cytokines. © 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. All rights reserved
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    Publication
    Herpesviruses viral loads and levels of proinflammatory cytokines in apical periodontitis
    (2018)
    Jakovljevic, A. (56396874600)
    ;
    Knezevic, A. (22034890600)
    ;
    Nikolic, N. (55324775800)
    ;
    Soldatovic, I. (35389846900)
    ;
    Jovanovic, T. (26642921700)
    ;
    Milasin, J. (6603015594)
    ;
    Andric, M. (20435687400)
    Objectives: This study aimed to analyse Epstein–Barr virus (EBV) and human cytomegalovirus (HCMV) viral loads in symptomatic and asymptomatic apical periodontitis lesions, to determine levels of TNF-α, IL-1β and IL-6 in these lesions and to investigate a possible correlation between herpesviral copy numbers and levels of proinflammatory cytokines. Materials and Methods: A total of 100 samples of apical periodontitis were subjected to HCMV and EBV copy numbers analysis by nested polymerase chain reaction (PCR) and TaqMan real-time PCR. The concentrations of TNF-α, IL-1β and IL-6 were determined by ELISA method. SPSS software was used for statistical analysis. Results: There were no significant differences in the occurrence of EBV and HCMV between symptomatic and asymptomatic periapical lesions (p =.686, p =.879, respectively). Only 12 of 74 EBV (16.2%) and four of 54 HCMV (13.5%) nested PCR-positive samples showed increased viral copy numbers above the limit of 125 copies/ml. There was no significant correlation between the levels of analysed proinflammatory cytokines and herpesviral copy numbers in our sample. Conclusion: The observed low viral loads point to a relatively rare occurrence of active EBV and HCMV infection in our sample. Latent herpesviral infection does not enhance the production of investigated proinflammatory cytokines. © 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. All rights reserved
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    Human cytomegalovirus is present in odontogenic cysts
    (2007)
    Andric, M. (20435687400)
    ;
    Milasin, J. (6603015594)
    ;
    Jovanovic, T. (26642921700)
    ;
    Todorovic, L. (56715610800)
    Introduction: Recent studies suggest that some viruses, including human cytomegalovirus (CMV), may be involved in the pathogenesis of periapical lesions. Since periapical cysts (PCs) represent the next stage in the evolution of periapical granuloma, it seemed reasonable to investigate the presence of CMV in PCs and any possible relationship between its presence and the clinical features of those cysts, as well as to compare the results obtained with corresponding findings in non-inflammatory lesions, like odontogenic keratocysts (OKCs). Methods: Samples of 33 PCs and 10 OKCs, obtained at the time of surgery, were used for the detection of CMV DNA by polymerase chain reaction. Presence of the virus was correlated with clinical and radiographic features of the cysts. Results: CMV was detected in 18 PCs (54.5%) and six OKCs (60%). The presence of CMV was more frequent in cyst samples collected from patients who reported previous episodes of acute infection. The presence of sinus tract was more frequent in CMV-positive cysts and CMV presence was less frequent in a group of cysts showing signs of acute inflammation at the time of sample collection. The mean sizes of CMV-positive and CMV-negative PCs were almost the same; CMV-positive OKCs were slightly larger than CMV-negative OKCs. None of these results proved to be statistically significant. Conclusion: The presence of CMV in the cystic wall is a common feature of both inflammatory and non-inflammatory odontogenic cysts. Although this study has not proved that CMV affects pathogenesis of odontogenic cysts, such a possibility could not be ruled out. © 2007 The Authors.
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    Human cytomegalovirus is present in odontogenic cysts
    (2007)
    Andric, M. (20435687400)
    ;
    Milasin, J. (6603015594)
    ;
    Jovanovic, T. (26642921700)
    ;
    Todorovic, L. (56715610800)
    Introduction: Recent studies suggest that some viruses, including human cytomegalovirus (CMV), may be involved in the pathogenesis of periapical lesions. Since periapical cysts (PCs) represent the next stage in the evolution of periapical granuloma, it seemed reasonable to investigate the presence of CMV in PCs and any possible relationship between its presence and the clinical features of those cysts, as well as to compare the results obtained with corresponding findings in non-inflammatory lesions, like odontogenic keratocysts (OKCs). Methods: Samples of 33 PCs and 10 OKCs, obtained at the time of surgery, were used for the detection of CMV DNA by polymerase chain reaction. Presence of the virus was correlated with clinical and radiographic features of the cysts. Results: CMV was detected in 18 PCs (54.5%) and six OKCs (60%). The presence of CMV was more frequent in cyst samples collected from patients who reported previous episodes of acute infection. The presence of sinus tract was more frequent in CMV-positive cysts and CMV presence was less frequent in a group of cysts showing signs of acute inflammation at the time of sample collection. The mean sizes of CMV-positive and CMV-negative PCs were almost the same; CMV-positive OKCs were slightly larger than CMV-negative OKCs. None of these results proved to be statistically significant. Conclusion: The presence of CMV in the cystic wall is a common feature of both inflammatory and non-inflammatory odontogenic cysts. Although this study has not proved that CMV affects pathogenesis of odontogenic cysts, such a possibility could not be ruled out. © 2007 The Authors.
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    Survivin expression in odontogenic keratocysts and correlation with cytomegalovirus infection
    (2010)
    Andric, M. (20435687400)
    ;
    Dozic, B. (6507142704)
    ;
    Popovic, B. (7006225668)
    ;
    Stefanovic, D. (59428781400)
    ;
    Basta-Jovanovic, G. (6603093303)
    ;
    Djogo, N. (33367776900)
    ;
    Andjus, P. (6603805616)
    ;
    Milasin, J. (6603015594)
    Objectives: The aim of this study was to investigate the expression of survivin, an inhibitor of apoptosis, in odontogenic keratocysts and to compare it to the findings in non-neoplastic jaw cysts - periapical cysts, as well as to establish a possible relationship between survivin expression and human cytomegalovirus presence within these cysts. Materials and methods: Samples of 10 odontogenic keratocysts (five positive and five negative for the presence of cytomegalovirus, as determined by polymerase chain reaction) and 10 periapical cysts (five positive and five negative for the cytomegalovirus presence) were analysed. The expression of survivin was assessed by immunohistochemical methods, using monoclonal antibody that selectively recognizes the cytoplasmic form of survivin. Results: All 10 odontogenic keratocysts showed immunostaining for survivin, while all 10 periapical cysts were negative for its presence. There was no correlation between cytomegalovirus presence and expression of survivin within odontogenic keratocysts. Conclusion: Survivin may contribute to the aggressive behavior of odontogenic keratocysts, and thus support the emerging opinion of their neoplastic nature. © 2009 John Wiley & Sons A/S.
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    Publication
    Survivin expression in odontogenic keratocysts and correlation with cytomegalovirus infection
    (2010)
    Andric, M. (20435687400)
    ;
    Dozic, B. (6507142704)
    ;
    Popovic, B. (7006225668)
    ;
    Stefanovic, D. (59428781400)
    ;
    Basta-Jovanovic, G. (6603093303)
    ;
    Djogo, N. (33367776900)
    ;
    Andjus, P. (6603805616)
    ;
    Milasin, J. (6603015594)
    Objectives: The aim of this study was to investigate the expression of survivin, an inhibitor of apoptosis, in odontogenic keratocysts and to compare it to the findings in non-neoplastic jaw cysts - periapical cysts, as well as to establish a possible relationship between survivin expression and human cytomegalovirus presence within these cysts. Materials and methods: Samples of 10 odontogenic keratocysts (five positive and five negative for the presence of cytomegalovirus, as determined by polymerase chain reaction) and 10 periapical cysts (five positive and five negative for the cytomegalovirus presence) were analysed. The expression of survivin was assessed by immunohistochemical methods, using monoclonal antibody that selectively recognizes the cytoplasmic form of survivin. Results: All 10 odontogenic keratocysts showed immunostaining for survivin, while all 10 periapical cysts were negative for its presence. There was no correlation between cytomegalovirus presence and expression of survivin within odontogenic keratocysts. Conclusion: Survivin may contribute to the aggressive behavior of odontogenic keratocysts, and thus support the emerging opinion of their neoplastic nature. © 2009 John Wiley & Sons A/S.

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