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慢性淋巴细胞白血病患者 HLA-G 和 TLR-9 的总表达。

Total expression of HLA-G and TLR-9 in chronic lymphocytic leukemia patients.

机构信息

Department of Experimental Hematooncology, Medical University of Lublin, 20950 Lublin, Poland.

出版信息

Hum Immunol. 2013 Dec;74(12):1592-7. doi: 10.1016/j.humimm.2013.08.277. Epub 2013 Aug 29.

Abstract

Suppressed immune status facilitates immune escape mechanisms that allow chronic lymphocytic leukemia cells to proliferate and expand. The expression of HLA-G could effectively inhibit the immune response. In immune response inhibitory signals follow activation of immune system which might be occur during bacterial or viral infection in CLL patients. In the current study we characterized two components of immune system, inhibitory molecule HLA-G with its receptor - CD85j and Toll-like receptor 9. The material was obtained from 41 CLL patients and 41 HV with similar median age. In CLL patients expression of intracellular and surface HLA-G and soluble HLA-G levels were significantly higher than in HV. We found higher expression of CD85j compared to HV and the positive correlation between expression of HLA-G and CD85j. All the CLL cells expressed TLR-9, and the level of expression positively correlated with expression of HLA-G and CD85j. Patients with higher expression of intracellular expression of TLR-9 have significantly longer treatment-free survival than patients with low expression of TLR-9 (57 months vs. 8 months, respectively). Summarizing in CLL we characterized activatory and inhibitory components of immune system that might be connected functionally. Analysis of TLR-9 expression might have additional prognostic value for CLL patients.

摘要

受抑制的免疫状态促进了慢性淋巴细胞白血病细胞的增殖和扩增的免疫逃逸机制。HLA-G 的表达可以有效地抑制免疫反应。在免疫反应抑制信号遵循免疫系统的激活,这可能发生在慢性淋巴细胞白血病患者的细菌或病毒感染期间。在本研究中,我们研究了两个免疫系统的抑制分子 HLA-G 及其受体 CD85j 和 Toll 样受体 9。从 41 例慢性淋巴细胞白血病患者和 41 例 HV 中获得了材料,这些患者的中位年龄相似。与 HV 相比,慢性淋巴细胞白血病患者的细胞内和表面 HLA-G 表达以及可溶性 HLA-G 水平明显更高。与 HV 相比,我们发现 CD85j 的表达更高,并且 HLA-G 和 CD85j 的表达之间存在正相关。所有慢性淋巴细胞白血病细胞均表达 TLR-9,其表达水平与 HLA-G 和 CD85j 的表达呈正相关。与 TLR-9 低表达的患者相比,细胞内 TLR-9 表达较高的患者无治疗生存时间明显更长(分别为 57 个月和 8 个月)。总之,在慢性淋巴细胞白血病中,我们描述了可能具有功能联系的免疫系统的激活和抑制成分。TLR-9 表达的分析可能对慢性淋巴细胞白血病患者具有额外的预后价值。

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