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作 者:贺联印[1] 王京华[1] 王申五[1] 杨铁生[1] 杜绍财[1] 樊春红[1]
机构地区:[1]北京医科大学人民医院
出 处:《中华医学杂志》1994年第2期97-99,T013,共4页National Medical Journal of China
摘 要:为了进一步证实EB病毒与干燥综合征发病的关系,作者设计了EB病毒BamW片段特异的引物和寡核苷酸探针,利用PCR体外基因扩增方法和核酸分子杂交技术检测出干燥综合征患者外周血白细胞及唇腺组织中存在有高频率的EB病毒DNA,而对照组的阳性率相对很低。用原位杂交方法检测干燥综合征患者唇腺组织中EB病毒DNA,共28例中有16例为阳性。结果说明干燥综合征患者EB病毒感染率较正常人明显增高,且EB病毒感染与靶器官的损害有关,提示靶器官控制EB病毒细胞内复制的免疫机制出现异常。e designed a specific primer of EB virus Bam Wfragment and EBV DNA sequence by using thepolymerase chain reaction (PCR) to amplify the EBVDNA sequences and then performing thehybndization analysis (dot blot and Southern transfer)with a end-labelled internal oligonucleotideprobe. There was significantly higher positive rate of24% (7/29) for the labial glands of SJbgren'ssyndrome patients than 68% (20/29) for p Bam Wprobe. In situ DNA hybridization, with (a35S) DCTPlabelled EBV DNA probe, the EBV genomes weredemonstrated in the labial glands of the Suogren'ssyndrome patients (l6/28). Moreover. the elevatedcontent of EBV DNA was identified in those withmore severe destruction of labial glands. We concludethat EBV has a normal site of latency at saliveryglands in a nonpathogenic state, and may be reactivat-ed in SJtigren's syndrome patients and play a role inthe pathogenesis on this disease. The great sensitivityof PCR and the ability to analyze very small tissuebiopsies (fresh or paraffin embedded) make this tech-nique applicable to clinical diagnosis.
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