HLA区域的遗传标记可识别RA受试者中结核病风险的患者

G. Lugo-Zamudio, R. Barbosa-Cobos, D. Delgado-Ochoa, Rodrigo Arreola
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引用次数: 1

摘要

目的:确定RA患者在使用抗肿瘤坏死因子生物治疗前发生结核病的最高风险。方法:我们进行了两阶段的研究,分为三组,第一阶段我们在墨西哥华雷斯医院进行了病例和对照研究,第二阶段,将第一阶段的结果与庞塞病确诊患者组的结果进行了分析。我们比较了首次接受生物治疗的患者和健康对照者的HLA I类和II类。结果:我们已经确定了几个候选等位基因,这些等位基因将有助于推进RA的个性化治疗,同时考虑到发展为TB的遗传风险,特别是等位基因B27和DQB1*0301。结论:类风湿性关节炎患者发展为结核病和由此产生的严重并发症的风险增加。这种感染过程与生物制剂的使用有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic markers in HLA region to identify patients with tuberculosis risk, in RA subjects
Objetive: To identify the patients with RA at highest risk of TB, prior to the use of biological therapy antiTNF. Method: We carried out a study of two phases considered three groups, in the first we performed a case and control study in the Hospital Juarez de Mexico, in the second phase, the results of phase one were analyzed with those obtained in the group of patients identified with Poncet´s disease. We compared the classes I and II of the HLA of patients naive to biologic treatment with healthy controls. Result: We have identified several candidate alleles that will help to advance the personalized treatment of RA that takes into account the genetic risk to develop TB, particularly the alleles B27 and DQB1*0301. Conclusion: Patients with RA have an increased risk to develop TB and severe complications derived from it. This infectious process is related to the use of biologic.
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