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001-es BibID:BIBFORM013305
Első szerző:Radics Tünde (egyetemi adjunktus, fogszakorvos)
Cím:Interleukin-6 and granulocytemacrophage colony-stimulating factor in apical periodontitis : correlation with clinical and histologic findings of the involved teeth / T. Radics, C. Kiss, I. Tar, I. J. Márton
Dátum:2003
ISSN:0902-0055
Megjegyzések:Apical periodontitis is characterized by the presence of immunocompetent cells producing a wide variety of inflammatory mediators. Releasing cytokines with long-range action, such as interleukin-6 (IL-6) and granulocyte-macrophage colony-stimulating factor (GM-CSF), apical periodontitis may induce changes in remote organs of the host. This study quantified the levels of IL-6 and GM-CSF in symptomatic and asymptomatic human periradicular lesions. Lesions were also characterized by size and histologic findings. Tissue samples were homogenized and supernatants were assayed using an enzyme-linked immunosorbent assay (ELISA). Correlations between cytokine levels and characteristic features (as single variables) of the lesions were analysed. There was a trend for higher levels of IL-6 and GM-CSF in symptomatic than in asymptomatic lesions, but the difference was not significant. Levels also tended to be higher in large than in small lesions, in polymorphonuclear (PMN) cell-rich than in PMN cell-poor samples, and in epithelialized than in non-epithelialized lesions. Significantly higher levels of IL-6 (778.1 +/- 220.5 pg/microg) and GM-CSF (363.3 +/- 98.4 pg/microg) were found in samples coincidentally possessing symptomatic and epithelialized features than in asymptomatic, small, PMN cell-poor, non-epithelialized lesions (IL-6: 45.2 +/- 13.1 pg/microg and GM-CSF: 135.1 +/- 26.4 pg/microg). These results suggest that symptomatic lesions containing epithelial cells represent an immunologically active stage of apical periodontitis, whereas asymptomatic, small, PMN cell-poor, non-epithelialized lesions represent healing apical lesions.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
cytokines
granulocytemacrophage
colony-stimulating factor
interleukin-6
periodontitis
Megjelenés:Oral Microbiology And Immunology. - 18 : 1 (2003), p. 9-13. -
További szerzők:Kiss Csongor (1956-) (hematológus, onkológus) Tar Ildikó (1967-) (fogszakorvos) Márton Ildikó (1954-) (fogszakorvos)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
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2.

001-es BibID:BIBFORM008946
Első szerző:Szarka Krisztina (molekuláris biológus, mikrobiológus)
Cím:Progressive increase of human papillomavirus carriage rates in potentially malignant and malignant oral disorders with increasing malignant potential / Szarka Krisztina, Tar Ildikó, Fehér Enikő, Gáll Tamás, Kis Andrea, D. Tóth Etelka, Boda Róbert, Márton Ildikó, Gergely Lajos
Dátum:2009
Megjegyzések:We investigated the potential role of human papillomaviruses (HPVs) in potentially malignant oral disorders, oral leukoplakia (OL) and oral lichen planus (OLP), and in oral squamous cell cancer (OSCC) in an Eastern Hungarian population with a high incidence of OSCC. Methods: Excised tumor samples (65 OSCC patients) and exfoliated cells from potentially malignant lesions (from 44 and 119 patients with OL and OLP, respectively) as well as from healthy controls (72 individuals) were analysed. OLPs were classified based on clinical appearance, 61 patients had erosive?atrophic lesions (associated with higher malignancy risk, EA-OLP) and 58 had non-erosive non-atrophic lesions (with lower risk of becoming malignant, non-EA-OLP), respectively. Exfoliated cells collected from apparently healthy mucosa accompanied each lesion sample. HPV was detected by MY/GP polymerase chain reaction (PCR) and genotyped by restriction analysis of amplimers. Copy numbers in lesions were determined using real-time PCR. Prevalence rates, copy number distributions, and association with risk factors and diseases were analysed using chi-square test, t-test, and logistic regression, respectively. Results: We detected HPVs significantly more frequently in lesions than in controls (P ? 0.001 in all comparisons). HPV prevalence increased gradually with increasing severity of lesions (32.8, 40.9, and 47.7% in OLP, OL, and OSCC, respectively). Copy number distribution patterns roughly corresponded to prevalence rates, but OLP and OL were comparable. HPV prevalence differed significantly between EA-OLP and non-EA-OLP groups (42.6 vs. 22.4%); EA-OLP group showed a prevalence similar to that found in OL. Conclusion: HPVs may be involved in the development or progression of not only OSCC but also of potentially malignant oral lesions.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
human papillomavirus
oral carcinogenesis
Megjelenés:Oral Microbiology and Immunology 24 : 4 (2009), p. 314-318. -
További szerzők:Tar Ildikó (1967-) (fogszakorvos) Fehér Enikő (1981-) (molekuláris biológus, mikrobiológus) Gáll Tamás (1982-) (molekuláris biológus, mikrobiológus) Kis Andrea (1981-) (molekuláris biológus, mikrobiológus) D. Tóth Etelka (1975-) (fogszakorvos) Boda Róbert (1978-) (fogszakorvos) Márton Ildikó (1954-) (fogszakorvos) Gergely Lajos (1940-) (szakorvos, klinikai mikrobiológus)
Internet cím:elektronikus változat
DOI
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