O'Brien-Simpson N M, Black C L, Bhogal P S, Cleal S M, Slakeski N, Higgins T J, Reynolds E C
Oral Health Sciences Unit, School of Dental Science, The University of Melbourne, Melbourne, Victoria 3000, Australia.
Infect Immun. 2000 May;68(5):2704-12. doi: 10.1128/IAI.68.5.2704-2712.2000.
Serum immunoglobulin G (IgG), IgM, and IgG subclass responses to the RgpA-Kgp proteinase-adhesin complex of Porphyromonas gingivalis were examined by enzyme-linked immunosorbent assay using adult periodontitis patients and age- and sex-matched controls. Twenty-five sera from subjects with adult periodontitis (diseased group) and 25 sera from healthy subjects (control group) were used for the study. Sera and subgingival plaque samples from 10 sites were collected from each patient at the time of clinical examination. The level of P. gingivalis in the plaque samples was determined using a DNA probe. Highly significant positive associations between the percentage of sites positive for P. gingivalis and measures of disease severity (mean pocket depth, mean attachment loss, and percentage of sites that bled on probing) were found. The diseased group had significantly higher specific IgG responses to the RgpA-Kgp complex than did the control group, and the responses were significantly associated with mean probing depths and percentage of sites positive for P. gingivalis. Analysis of the IgG subclass responses to the RgpA-Kgp complex revealed that the subclass distribution for both the diseased and control groups was IgG4 > IgG2 > IgG3 = IgG1. The IgG2 response to the complex was positively correlated with mean probing depth, whereas the IgG4 response was negatively correlated with this measure of disease severity. Immunoblot analysis of the RgpA-Kgp complex showed that sera from healthy subjects and those with low levels of disease, with high IgG4 and low IgG2 responses, reacted with the RgpA27, Kgp39, and RgpA44 adhesins; however, sera from diseased subjects with low IgG4 and high IgG2 responses reacted only with the RgpA44 and/or Kgp44 adhesins. Epitope mapping of the RgpA27 adhesin localized a major epitope recognized by IgG4 antibodies in sera from subjects with high IgG4 and low IgG2 responses to the RgpA-Kgp complex which was not recognized by sera from diseased subjects with low IgG4 and high IgG2 responses.
通过酶联免疫吸附测定法,使用成年牙周炎患者以及年龄和性别匹配的对照组,检测了血清免疫球蛋白G(IgG)、IgM以及对牙龈卟啉单胞菌RgpA-Kgp蛋白酶-黏附素复合物的IgG亚类反应。本研究使用了来自成年牙周炎患者(疾病组)的25份血清和来自健康受试者(对照组)的25份血清。在临床检查时,从每位患者的10个部位采集血清和龈下菌斑样本。使用DNA探针测定菌斑样本中牙龈卟啉单胞菌的水平。发现牙龈卟啉单胞菌阳性部位的百分比与疾病严重程度指标(平均牙周袋深度、平均附着丧失以及探诊出血部位的百分比)之间存在高度显著的正相关。疾病组对RgpA-Kgp复合物的特异性IgG反应显著高于对照组,且这些反应与平均探诊深度以及牙龈卟啉单胞菌阳性部位的百分比显著相关。对RgpA-Kgp复合物的IgG亚类反应分析显示,疾病组和对照组的亚类分布均为IgG4 > IgG2 > IgG3 = IgG1。对该复合物的IgG2反应与平均探诊深度呈正相关,而IgG4反应与这种疾病严重程度指标呈负相关。RgpA-Kgp复合物的免疫印迹分析表明,来自健康受试者以及疾病程度较低、IgG4反应高且IgG2反应低的受试者的血清,与RgpA27、Kgp39和RgpA44黏附素发生反应;然而,来自疾病程度较高、IgG4反应低且IgG2反应高的受试者的血清仅与RgpA44和/或Kgp44黏附素发生反应。RgpA27黏附素的表位作图将高IgG4和低IgG2反应的受试者血清中被IgG4抗体识别的主要表位定位在RgpA-Kgp复合物上,而低IgG4和高IgG2反应的疾病受试者血清则不识别该表位。
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