首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >IL-10 Promoter Gene Polymorphism Associated with the Occurrence of Chronic GVHD and Its Clinical Course During Systemic Immunosuppressive Treatment for Chronic GVHD after Allogeneic Peripheral Blood Stem Cell Transplantation.
【24h】

IL-10 Promoter Gene Polymorphism Associated with the Occurrence of Chronic GVHD and Its Clinical Course During Systemic Immunosuppressive Treatment for Chronic GVHD after Allogeneic Peripheral Blood Stem Cell Transplantation.

机译:同种异体外周血干细胞移植后系统性免疫抑制治疗慢性GVHD的过程中,IL-10启动子基因多态性与慢性GVHD的发生及其临床过程有关。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND.: The current study attempted to evaluate the association between IL-10 promoter gene polymorphism and transplant outcomes including the occurrence of chronic graft-versus-host disease (GVHD) and its clinical course during systemic immunosuppressive treatment (IST) among 60 recipients of cytokine-mobilized peripheral blood stem cell (PBSC) from HLA-matched sibling donors METHODS.: We analyzed 3 single-nucleotide polymorphisms in proximal region of IL-10 promoter gene (-1082/-819/-592). RESULTS.: In the current study, only two haplotypes (1082*A/819*T/592*A [ATA] and 1082*A/819*C/592*C [ACC]) were found. An increased occurrence of chronic GVHD was noted dependent on the IL-10 haplotypes (43% vs. 68% vs. 96% in ACC/ACC vs. ATA/ACC vs. ATA/ATA haplotype, P=0.003). In a logistic regression based on multinomial model, ATA/ATA homozygote had 7-fold increasing risk of the development of chronic GVHD compared with ACC/ACC homozygote. The incidence of chronic GVHD at 1 year was 46%+/-20%, 64%+/-10%, and 82%+/-5% in ACC/ACC, ATA/ACC and ATA/ATA group, respectively (P=0.0266). Plus, the duration of systemic IST was significantly shorter in recipients without ATA-haplotype comparing with those with ATA haplotype (339 days vs. 1,146 days, P=0.0091). CONCLUSION.: IL-10 promoter gene polymorphism was found to be apparently associated with chronic GVHD after allogeneic peripheral blood stem cell transplantation from HLA-matched sibling donors.
机译:背景:目前的研究试图评估IL-10启动子基因多态性与移植结局之间的关联,包括在系统性免疫抑制治疗(IST)期间接受免疫治疗的60位接受者中的慢性移植物抗宿主病(GVHD)的发生及其临床过程。方法:我们分析了IL-10启动子基因(-1082 / -819 / -592)近端区域中的3个单核苷酸多态性。结果:在当前研究中,仅发现了两种单体型(1082 * A / 819 * T / 592 * A [ATA]和1082 * A / 819 * C / 592 * C [ACC])。注意到慢性GVHD发生率的增加取决于IL-10单倍型(ACC / ACC vs. ATA / ACC vs. ATA / ATA单倍型分别为43%vs. 68%vs. 96%,P = 0.003)。在基于多项模型的逻辑回归中,与ACC / ACC纯合子相比,ATA / ATA纯合子患慢性GVHD的风险增加了7倍。 ACC / ACC,ATA / ACC和ATA / ATA组在1年时慢性GVHD的发生率分别为46%+ /-20%,64%+ /-10%和82%+ /-5%(P = 0.0266)。另外,与没有ATA单倍型的受者相比,全身IST的持续时间明显短于没有ATA单倍型的受者(339天vs. 1,146天,P = 0.0091)。结论:从HLA匹配的同胞供体同种异体外周血干细胞移植后,发现IL-10启动子基因多态性与慢性GVHD明显相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号