首都医科大学学报 ›› 1997, Vol. 18 ›› Issue (2): 139-142.

• 论著 • 上一篇    下一篇

HLA-DR位点基因分型在肾移植配型中的应用研究

薛竹, 尔秀江, 张玉海, 马威然, 李哲先, 毕如玫, 武俊杰   

  1. 首都医科大学附属北京友谊医院泌尿科
  • 收稿日期:1996-07-17 修回日期:1900-01-01 出版日期:1997-04-15 发布日期:1997-04-15

Gene Typing HLA-DR for Research of Renal Transplantation

Xue Zhu, Er Xiujiang, Zhang Yuhai, Ma Weiran, Li Zhexian, Bi Rumei, Wu Junjie   

  1. Department of Urology Institute, Beijing Friendship Hospital, Affiliate of Capital University of Medical Sciences
  • Received:1996-07-17 Revised:1900-01-01 Online:1997-04-15 Published:1997-04-15

摘要: 应用聚合酶链式反应序列特异性引物(PCR-SSP)技术,对331例肾移植供受者进行HLA-DR位点基因分型,其中109例同时与血清学分型进行对比研究.显示血清学方法误差率为29.7%;而PCR-SSP法的DR位点分型,所有特异性均能显示,无假阴性及假阳性.随机抽取的20例样本进行重复实验,重复性为100%.分型结果经INNO-LIPAPCR-反向SSO实验确证,符合率为100%.此方法耗时4h,较血清学方法操作简便、快速、结果准确可靠,适合于临床器官移植HLA分型.

关键词: 聚合酶链式反应, 序列特异性引物, 基因分型

Abstract: In order to select donor and recipient,accurate typing HLAespecially typing HLA-DR is one of the most important factor for a longer survival time of the graft.Using polymerase chain reaction with sequence specific primers(PCR-SSP)technique the authors underwent HLA-DR gene typing in 331 cases of donor and recipient. Among them,109 cases were subjected to a comparative study with serological typing. The results showed that the error rate of serological assay was 29.7%, while the HLA-DRgene typing with PCR-SSP method all showed their specificities without any false negative or false positive.Replication experiments in 20 cases of random sampling showed 100% coincidence. The typing results were confirmed by INNO-LIPA PCR-Reverse SSOexperiments,and the coincidence was 100%. Only 4 hours will suffice for this assay. So, it is simple, rapid and reliable as compared with the serological method, and is suitable for HLAtyping in clinical organ transplantation.

Key words: polymerase chain reaction(PCR), sequence specific primers(SSP), gene typing

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