Nepom G T, Gersuk V, Nepom B S
Virginia Mason Research Center and the University of Washington School of Medicine, Seattle, WA, USA.
J Rheumatol Suppl. 1996 Mar;44:5-9.
Current methods and approaches for the use of HLA markers in the assessment of rheumatoid arthritis (RA) are not optimal. Improved strategies for application of HLA susceptibility genetic typing in patients were evaluated and a new system for rapid determination of these RA susceptibility alleles was developed. Retrospective data summarizing the prevalence of HLA susceptibility alleles in patients with distinct clinical outcomes was analyzed to estimate the sensitivity and specificity of HLA genetic testing as a prognostic marker for erosive disease. A rapid allele specific DNA hybridization assay was performed on an automated instrument using a solid phase nonradioactive hybridization and detection system. Depending on the patient population being tested, from 70-80 percent of patients with progressive erosive disease carry one or more of the DR4 cluster of RA susceptibility genes (DRB1*0401, 0404, 0405). Sensitivity is increased by including other shared epitope positive alleles, but at the expense of specificity. The rapid automated genetic testing system correctly identified each of more than 200 samples tested, with no false positives. HLA genetic testing for RA susceptibility alleles can be performed rapidly and accurately. Prognosis for erosive disease can be facilitated in the patient with early pre-erosive RA using HLA testing in combination with other clinical assessment variables.
目前在类风湿关节炎(RA)评估中使用HLA标记物的方法和途径并不理想。对改善HLA易感性基因分型在患者中的应用策略进行了评估,并开发了一种快速确定这些RA易感性等位基因的新系统。分析了总结不同临床结局患者中HLA易感性等位基因流行情况的回顾性数据,以评估HLA基因检测作为侵蚀性疾病预后标志物的敏感性和特异性。使用固相非放射性杂交和检测系统在自动化仪器上进行快速等位基因特异性DNA杂交检测。根据所检测的患者群体,70%至80%的进行性侵蚀性疾病患者携带一个或多个RA易感性基因的DR4簇(DRB1*0401、0404、0405)。纳入其他共享表位阳性等位基因可提高敏感性,但会牺牲特异性。快速自动化基因检测系统正确识别了所检测的200多个样本中的每一个,无假阳性。RA易感性等位基因的HLA基因检测可快速、准确地进行。对于早期侵蚀前RA患者,结合其他临床评估变量进行HLA检测有助于预测侵蚀性疾病的预后。