Journal Of Clinical Periodontology · 1986 · 35 citations · 25 references
DentistryPathobiologyPeriodonticsInflammationPeriodontal BiologyPeriodontal MedicineHost Immune ResponsePeriodontal DiseasePeriodontal ImmunologyPeriodontal InflammationAssayImmunopathogenesis Of PeriodontitisPeriodontitis PathogenesisPlasma ComponentsPlasma Protein AnalysisPro-inflammatory Mediators In PeriodontitisReference Sera
The generation rate of free oxygen radicals as measured by maximal light intensity of luminol-enhanced chemiluminescence from peripheral blood granulocytes (PMN) stimulated with differently opsonized Staphylococcus aureus was studied in 13 patients with juvenile periodontitis (JP) and pair-matched, healthy controls. Plasma proteins related to inflammation were also assayed. When stimulated with bacteria opsonized with autologous serum, the PMN from the JP patients showed a more intensive chemiluminescence than did their pair-matched controls (p less than or equal to 0.0005). The difference was consistent but slightly reduced when using heat-treated serum (p less than or equal to 0.006) or heterologous gammaglobulin (p less than or equal to 0.19) for opsonization. When testing freeze preserved sera from 11 of the compared pairs, the sera from JP patients induced a slightly higher chemiluminescence in PMN from a healthy donor (p less than or equal to 0.031). Protein analysis of the patient sera revealed a slightly higher concentration of complement 4 (p less than or equal to 0.032) and IgM (p less than or equal to 0.030) when compared with their respective pair-matched healthy controls. The influence of other blood components contaminating our assay system was checked on healthy PMN cells. Lymphocytes, platelets, relevant amounts of ADP and serum had no effect on the chemiluminescence. In conclusion, the increased chemiluminescence of peripheral blood granulocytes from patients with juvenile periodontitis seems to be related mainly to the cells. The association with free oxygen radicals and their tissue-damaging potency might be a contributing factor in the pathogenesis of periodontal disease.
25
Oxygen-Dependent Microbial Killing by Phagocytes
Bernard Babior · New England Journal of Medicine · 1978 · 2.5K citations
Neutrophil Chemotaxis Dysfunction in Human Periodontitis
Thomas E. Van Dyke, H. U. Horoszewicz, L. J. Cianciola et al. · Infection and Immunity · 1980 · 298 citations · Full text
Defective neutrophil chemotaxis in juvenile periodontitis
Robert A. Clark, Roy C. Page, Greggory Wilde · Infection and Immunity · 1977 · 267 citations · Full text
Dentistry, Pediatrics, Periodontics +16