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受体 CXCL10 + 1642C>G 变异预测 HLA 全匹配无关骨髓移植后的生存结局。

The recipient CXCL10 + 1642C>G variation predicts survival outcomes after HLA fully matched unrelated bone marrow transplantation.

机构信息

Department of Hematology and Oncology, Kanazawa University Hospital, Kanazawa, Japan.

出版信息

Clin Immunol. 2013 Feb;146(2):104-11. doi: 10.1016/j.clim.2012.11.009. Epub 2012 Dec 7.

Abstract

CXCL10 is a chemoattractant for immune cells that is involved in several immune-inflammatory disorders. This study retrospectively examined the impact of a single nucleotide variation (rs3921, +1642C>G) in the CXCL10 gene on transplant outcomes in a cohort of 652 patients who underwent unrelated HLA-matched bone marrow transplantation (BMT) for hematologic malignancies. The recipient C/G or G/G genotype was found to be associated with a significantly better 5-year overall survival (OS) rate and a lower transplant-related mortality (TRM) rate than the recipient C/C genotype. The recipient C/G or G/G genotype also predicted a reduced incidence of death due to organ failure. The multivariate analysis showed the recipient C/G or G/G genotype to exhibit statistical trends toward beneficial effects on OS but not on TRM. CXCL10 genotyping could therefore be useful in predicting prognoses and creating therapeutic strategies for improving the final outcomes of patients who undergo allogeneic BMT.

摘要

趋化因子配体 10(CXCL10)是一种参与多种免疫炎症性疾病的免疫细胞趋化因子。本研究回顾性分析了 652 例接受无关 HLA 匹配骨髓移植(BMT)治疗血液系统恶性肿瘤患者中 CXCL10 基因单个核苷酸变异(rs3921,+1642C>G)对移植结果的影响。与受体 C/C 基因型相比,受体 C/G 或 G/G 基因型的患者 5 年总生存率(OS)显著提高,移植相关死亡率(TRM)降低。受体 C/G 或 G/G 基因型也降低了因器官衰竭导致的死亡发生率。多因素分析显示,受体 C/G 或 G/G 基因型对 OS 有统计学意义的有益影响,但对 TRM 无影响。因此,CXCL10 基因分型可能有助于预测预后,并制定改善接受异基因 BMT 患者最终结局的治疗策略。

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