Suppr超能文献

B型血友病和抗凝血因子IX抗体患者的基因缺失

Gene deletions in patients with haemophilia B and anti-factor IX antibodies.

作者信息

Giannelli F, Choo K H, Rees D J, Boyd Y, Rizza C R, Brownlee G G

出版信息

Nature. 1983;303(5913):181-2. doi: 10.1038/303181a0.

Abstract

Christmas disease, or haemophilia B, is an inherited X-linked haemorrhagic disease which at present occurs in 798 known cases in the United Kingdom, corresponding to a frequency of about 1 in 30,000 males. Patients are deficient in the intrinsic clotting factor IX and are treated by replacement of this protein prepared from pooled plasma obtained from normal individuals. Occasionally treatment is complicated by the appearance of specific anti-factor IX antibodies. It seemed to us that this might be due to the absence of 'self' factor IX causing the immune system to regard the infused normal factor IX as foreign. The absence of all or part of the factor IX gene was an obvious possible reason for this, which we have now tested using our previously isolated gene probe. We have found four patients with gross gene defects.

摘要

克里斯马斯病,即血友病B,是一种遗传性X连锁出血性疾病,目前在英国有798例已知病例,男性发病率约为三万分之一。患者体内内源性凝血因子IX缺乏,通过输注从正常个体混合血浆中制备的该蛋白质进行治疗。偶尔,治疗会因特异性抗因子IX抗体的出现而变得复杂。在我们看来,这可能是由于缺乏“自身”因子IX,导致免疫系统将输注的正常因子IX视为外来物质。因子IX基因全部或部分缺失显然是一个可能的原因,我们现在使用之前分离的基因探针对此进行了检测。我们发现了四名存在严重基因缺陷的患者。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验