Califano J V, Schenkein H A, Tew J G
Clinical Research Center for Periodontal Diseases, School of Dentistry, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298.
Infect Immun. 1989 May;57(5):1582-9. doi: 10.1128/iai.57.5.1582-1589.1989.
This study was undertaken to look for characteristics of the immunodominant antigen(s) of Actinobacillus actinomycetemcomitans Y4 that might help explain the high antibody titers in periodontitis patients. Radioimmunoassays (RIA) were performed on sera from 481 patients; sera from the 32 patients with the highest anti-Y4 titers (above 128,000 RIA U/ml) were further analyzed. Y4 antigen was boiled for 45 min or treated with papain, and antibody responses were analyzed by RIA and Western blotting (immunoblotting). In addition, carbohydrate was purified from Y4 and examined by Western blotting. The results indicated that the immunodominant antigen of Y4 in high responders was stable after papain treatment or boiling for 45 min. Papain or boiling eliminated protein bands but a large diffuse band persisted on Western blots. With increasing dilutions of sera, bands on Western blots corresponding to protein antigens disappeared, while the large diffuse band resembling that of carbohydrate persisted. Partially purified Y4 carbohydrate contained the large diffuse band. Double-immunodiffusion analysis indicated that rabbit serotype b-specific antiserum and patient sera recognized the same antigen. When the carbohydrate extract was passed over a lipid A-binding column to remove lipopolysaccharide, the smear corresponding to the immunodominant antigen was still present on Western blots. The immunodominant antigen of Y4 in high-responder individuals appears to be a carbohydrate and is possibly the capsular polysaccharide.
本研究旨在寻找伴放线放线杆菌Y4免疫显性抗原的特征,这些特征可能有助于解释牙周炎患者体内的高抗体滴度。对481例患者的血清进行了放射免疫分析(RIA);对32例抗Y4滴度最高(高于128,000 RIA U/ml)患者的血清进行了进一步分析。将Y4抗原煮沸45分钟或用木瓜蛋白酶处理,然后通过RIA和蛋白质印迹法(免疫印迹法)分析抗体反应。此外,从Y4中纯化碳水化合物,并通过蛋白质印迹法进行检测。结果表明,高反应者中Y4的免疫显性抗原在木瓜蛋白酶处理或煮沸45分钟后仍稳定。木瓜蛋白酶处理或煮沸消除了蛋白条带,但蛋白质印迹上仍有一条大的弥散条带。随着血清稀释倍数增加,蛋白质印迹上与蛋白质抗原对应的条带消失,而类似于碳水化合物的大弥散条带依然存在。部分纯化的Y4碳水化合物含有这条大弥散条带。双向免疫扩散分析表明,兔b血清型特异性抗血清和患者血清识别相同抗原。当碳水化合物提取物通过脂多糖结合柱以去除脂多糖时,蛋白质印迹上对应免疫显性抗原的涂片仍然存在。高反应个体中Y4的免疫显性抗原似乎是一种碳水化合物,可能是荚膜多糖。