首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Soluble MICA as an independent prognostic factor for the overall survival and progression-free survival of multiple myeloma patients.
【24h】

Soluble MICA as an independent prognostic factor for the overall survival and progression-free survival of multiple myeloma patients.

机译:可溶性MICA是多发性骨髓瘤患者总体生存和无进展生存的独立预后因素。

获取原文
获取原文并翻译 | 示例
       

摘要

Major histocompatibility complex class I-related chain A (MICA) molecules are frequently expressed in lymphoproliferative malignancies including multiple myeloma (MM). MICA activates NK cells and co-stimulates T cells by interaction with its immunoreceptor NKG2D. In contrast, soluble MICA (sMICA) molecules impair the functions of NKG2D(+) T and NK cells, which may facilitate tumor cell escape from immunosurveillance. Here, we analyzed the clinical relevance of sMICA in 97 MM patients. sMICA (mean+/-SEM pg/ml) was significantly increased (p<0.0001) in patients (429+/-20) compared to controls (230+/-20; N=43). Serial determination showed a strong correlation between increments of sMICA and paraprotein levels (r=0.543, p<0.0001, N=49). sMICA levels >305 pg/ml are associated with a poor overall (p=0.004) and progression-free survival (p=0.002). Multivariate analysis revealed sMICA as an independent predictive factor for overall (p=0.007) and progression-free survival (p=0.002). Thus, our results suggest sMICA as a potent prognostic marker in MM, which may be useful to identify risk patients.
机译:主要的组织相容性复杂的I类相关链A(MICA)分子经常在包括多发性骨髓瘤(MM)在内的淋巴增生性恶性肿瘤中表达。 MICA通过与其免疫受体NKG2D的相互作用激活NK细胞并共同刺激T细胞。相比之下,可溶性MICA(sMICA)分子会损害NKG2D(+)T和NK细胞的功能,这可能有助于肿瘤细胞逃避免疫监视。在这里,我们分析了sMICA在97 MM患者中的临床相关性。与对照组(230 +/- 20; N = 43)相比,患者(429 +/- 20)的sMICA(平均值+/- SEM pg / ml)显着增加(p <0.0001)。连续测定显示sMICA的增加与副蛋白水平之间有很强的相关性(r = 0.543,p <0.0001,N = 49)。 sMICA水平> 305 pg / ml与总体不良(p = 0.004)和无进展生存期(p = 0.002)相关。多变量分析显示,sMICA是总体(p = 0.007)和无进展生存期(p = 0.002)的独立预测因子。因此,我们的研究结果提示sMICA作为MM的有效预后标志物,对识别危险患者可能有用。

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