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鉴定出一种与环孢素依赖性再生障碍性贫血易感性密切相关的特定HLA II类单倍型。

Identification of a specific HLA class II haplotype strongly associated with susceptibility to cyclosporine-dependent aplastic anemia.

作者信息

Nakao S, Takamatsu H, Chuhjo T, Ueda M, Shiobara S, Matsuda T, Kaneshige T, Mizoguchi H

机构信息

Third Department of Medicine, Kanazawa University School of Medicine, Japan.

出版信息

Blood. 1994 Dec 15;84(12):4257-61.

PMID:7994040
Abstract

Hematopoietic function of some aplastic anemia (AA) patients is dependent on the administration of cyclosporine (CyA). To investigate whether certain HLA class II genes are associated with susceptibility to such CyA-dependent AA, we determined the HLA class II alleles of 59 AA patients treated with CyA. Among 26 patients successfully treated with CyA, 13 required a small dose of CyA to maintain stable hematopoiesis. Of these 13 AA patients, 10 shared an HLA class II haplotype of DRB11501-DQA10102-DQB10602. None of the 13 responders who obtained a sustained remission off CyA therapy possessed this haplotype. In the 10 patients who shared the HLA class II haplotype, single-strand conformation polymorphism analysis of each gene fragment of this haplotype failed to detect a polymorphism in the nucleotide sequence. When the AA patients were assessed for their likelihood to respond to CyA therapy, the response rate in patients with this haplotype (71%) was significantly higher than that of patients with another haplotype associated with HLA-DR2, DRB11502-DQA10103-DQB10601 (36%) and that of patients without HLA-DR2 (35%). These findings indicate that the CyA-dependent response of AA is closely related to an HLA class II haplotype of DRB11501-DQA10102-DQB1*0602 and suggest that, in AA patients with this haplotype, immune mechanisms play an important role in the pathogenesis of bone marrow failure.

摘要

一些再生障碍性贫血(AA)患者的造血功能依赖于环孢素(CyA)的使用。为了研究某些人类白细胞抗原(HLA)Ⅱ类基因是否与这种依赖CyA的AA易感性相关,我们测定了59例接受CyA治疗的AA患者的HLAⅡ类等位基因。在26例成功接受CyA治疗的患者中,13例需要小剂量的CyA来维持稳定的造血功能。在这13例AA患者中,10例共享DRB11501-DQA10102-DQB10602的HLAⅡ类单倍型。在13例停止CyA治疗后获得持续缓解的反应者中,没有一例拥有这种单倍型。在共享该HLAⅡ类单倍型的10例患者中,对该单倍型各基因片段进行单链构象多态性分析,未检测到核苷酸序列多态性。当评估AA患者对CyA治疗的反应可能性时,具有这种单倍型的患者的反应率(71%)显著高于与HLA-DR2相关的另一种单倍型(DRB11502-DQA10103-DQB10601)的患者(36%)以及没有HLA-DR2的患者(35%)。这些发现表明,AA对CyA的依赖性反应与DRB11501-DQA10102-DQB1*0602的HLAⅡ类单倍型密切相关,并提示在具有这种单倍型的AA患者中,免疫机制在骨髓衰竭的发病机制中起重要作用。

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