McAtee C P, Lim M Y, Fung K, Velligan M, Fry K, Chow T, Berg D E
Genelabs Technologies, Inc., Redwood City, California 94063, USA.
Clin Diagn Lab Immunol. 1998 Jul;5(4):537-42. doi: 10.1128/CDLI.5.4.537-542.1998.
There is great interest in characterizing the proteins of the gastric pathogen Helicobacter pylori, especially those to which humans respond immunologically, because of the potential importance of such proteins in diagnosis and vaccine development. Two-dimensional gel electrophoresis was used to separate and identify potential antigens of H. pylori ATCC 43504. Over 30 proteins were reactive in Western blots with pooled sera from 14 infected patients. These proteins were analyzed by N-terminal sequence analysis. Fourteen proteins were determined to be distinct from any proteins previously described from H. pylori; the others were previously isolated and characterized proteins. Analysis of eight distinct H. pylori strains showed that most of these antigens were produced by all of the strains. We propose that collection of new antigens such as those recognized here will be useful in serologic tests for detecting and monitoring H. pylori infection and may also serve as potential targets for antimicrobial agent or vaccine development.
由于胃病原体幽门螺旋杆菌的蛋白质在诊断和疫苗开发中具有潜在重要性,因此人们对其进行表征,尤其是对那些能引起人体免疫反应的蛋白质,有着浓厚的兴趣。二维凝胶电泳被用于分离和鉴定幽门螺旋杆菌ATCC 43504的潜在抗原。超过30种蛋白质在Western印迹中与14名感染患者的混合血清发生反应。这些蛋白质通过N端序列分析进行了分析。确定有14种蛋白质与先前描述的幽门螺旋杆菌的任何蛋白质都不同;其他的是先前分离和表征过的蛋白质。对8种不同的幽门螺旋杆菌菌株的分析表明,这些抗原中的大多数由所有菌株产生。我们认为,收集诸如这里所识别的新抗原,将有助于用于检测和监测幽门螺旋杆菌感染的血清学检测,并且也可能作为抗菌剂或疫苗开发的潜在靶点。