Franca Mônica, Moura-Costa Lília, Meyer Roberto J, Trindade Soraya C, Tunes Urbino da Rocha, Freire Songelí M
Bahia State Foundation for the Development of Sciences, Salvador, BA, Brazil.
J Appl Oral Sci. 2007 Jun;15(3):213-9. doi: 10.1590/s1678-77572007000300011.
Periodontitis is a chronic disease that results from an interaction of a mixed bacterial challenge and the host response.
The purposes of this study were to evaluate the IgG serum levels to Porphyromonas gingivalis antigens by ELISA in individuals with different periodontal conditions correlated with clinical parameters, and to analyze the immunoreactivity profiles by Western blotting.
Serum IgG levels against the cell sonicate antigen from P. gingivalis ATCC 33277 of 28 patients with chronic periodontitis (CP), 10 patients with gingivitis (G) and 21 periodontally healthy individuals (H) were measured by ELISA and Western immunoblotting.
In the CP group, sera reactivity by ELISA was significantly higher than in the G and H groups (Kruskal-Wallis p<0.001; Dunnet t3 p= 0.001 and Dunnet t3 p= 0.0001). There was no statistically significant difference between G and HP reactivity (Dunnett t3 p=0.617). Among individuals with chronic periodontitis, the IgG-anti-P. gingivalis serum levels were positively correlated with percentage of clinical attachment level =5mm (r s = + 0.375, p<0.05) and a negative correlation was found between IgG-anti-P. gingivalis levels and percentage of probing pocket depth 0-3mm (r s = - 0. 411, p< 0.05). The analysis of sera immunoreactivity profiles to sonicate antigen by Western blotting showed differences between the sera of CP, G and H group individuals. The serum from CP frequently reacted with high molecular weight (103 kDa, 86 kDa, 72 kDa, 60 kDa, 58 kDa, 52 kDa) protein fractions.
Serum levels of IgG anti-P. gingivalis distinguished individuals with chronic periodontitis, gingivitis and healthy periodontium. There was a correlation between clinical parameters and serum IgG levels against P. gingivalis. There was a difference in the recognition profile of protein fractions among the studied groups and some bands were more specific.
牙周炎是一种由混合细菌挑战与宿主反应相互作用导致的慢性疾病。
本研究的目的是通过酶联免疫吸附测定(ELISA)评估不同牙周状况个体中针对牙龈卟啉单胞菌抗原的血清IgG水平,并将其与临床参数相关联,同时通过蛋白质印迹法分析免疫反应谱。
采用ELISA和Western免疫印迹法检测28例慢性牙周炎(CP)患者、10例牙龈炎(G)患者和21例牙周健康个体(H)血清中针对牙龈卟啉单胞菌ATCC 33277细胞超声破碎抗原的IgG水平。
在CP组中,ELISA检测的血清反应性显著高于G组和H组(Kruskal-Wallis检验p<0.001;Dunnet t3检验p = 0.001和Dunnet t3检验p = 0.0001)。G组和H组之间的反应性无统计学显著差异(Dunnett t3检验p = 0.617)。在慢性牙周炎患者中,抗牙龈卟啉单胞菌IgG血清水平与临床附着丧失≥5mm的百分比呈正相关(rs = + 0.375,p<0.0