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部分浆细胞分化是弥漫性大 B 细胞淋巴瘤中主要组织相容性复合体 II 类表达丢失的机制。

Partial plasma cell differentiation as a mechanism of lost major histocompatibility complex class II expression in diffuse large B-cell lymphoma.

机构信息

Department of Pathology, University of Arizona, 1501 N Campbell Avenue, Tucson, AZ 85724-5043, USA.

出版信息

Blood. 2012 Feb 9;119(6):1459-67. doi: 10.1182/blood-2011-07-363820. Epub 2011 Dec 13.

Abstract

Loss of major histocompatibility complex class II (MHC II) expression is associated with poor patient outcome in diffuse large B-cell lymphoma (DLBCL). As MHC II molecules are lost with plasmacytic differentiation in normal cells, we asked whether MHC II loss in DLBCL is associated with an altered differentiation state. We used gene expression profiling, quantum dots, and immunohistochemistry to study the relationship between MHC II and plasma cell markers in DLBCL and plasmablastic lymphoma (PBL). Results demonstrate that MHC II(-) DLBCL immunophenotypically overlap with PBL and demonstrate an inverse correlation between MHC II and plasma cell markers MUM1, PRDM1/Blimp1, and XBP1s. In addition, MHC II expression is significantly higher in germinal center-DLBCL than activated B cell-DLBCL. A minor subset of cases with an unusual pattern of mislocalized punctate MHC II staining and intermediate levels of mRNA is also described. Finally, we show that PBL is negative for MHC II. The results imply a spectrum of MHC II expression that is more frequently diminished in tumors derived from B cells at the later stages of differentiation (with complete loss in PBL). Our observations provide a possible unifying concept that may contribute to the poor outcome reported in all MHC II(-) B-cell tumors.

摘要

主要组织相容性复合体 II 类(MHC II)表达缺失与弥漫性大 B 细胞淋巴瘤(DLBCL)患者预后不良相关。由于 MHC II 分子在正常细胞的浆细胞分化过程中丢失,我们想知道在 DLBCL 中 MHC II 的丢失是否与分化状态的改变有关。我们使用基因表达谱分析、量子点和免疫组织化学来研究 DLBCL 和浆母细胞淋巴瘤(PBL)中 MHC II 与浆细胞标志物之间的关系。结果表明,MHC II(-)DLBCL 的免疫表型与 PBL 重叠,并显示 MHC II 与浆细胞标志物 MUM1、PRDM1/Blimp1 和 XBP1s 之间呈负相关。此外,MHC II 在生发中心-DLBCL 中的表达显著高于活化 B 细胞-DLBCL。还描述了一种具有异常点状 MHC II 染色和中等水平 mRNA 的罕见模式的亚组病例。最后,我们显示 PBL 对 MHC II 呈阴性。这些结果暗示存在 MHC II 表达谱,在源自分化后期 B 细胞的肿瘤中更为常见(在 PBL 中完全丢失)。我们的观察结果提供了一个可能的统一概念,这可能有助于解释所有 MHC II(-)B 细胞肿瘤报告的不良预后。

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