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CXCL13, CCL21, and CXCL12 expression in salivary glands of patients with Sjogren's syndrome and MALT lymphoma: Association with reactive and malignant areas of lymphoid organization

机译:干燥综合征和MALT淋巴瘤患者唾液腺中CXCL13,CCL21和CXCL12表达:与淋巴组织反应性和恶性区域相关

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摘要

The chemokines (CKs) CXCL13, CCL21, and CXCL12 are known to play differential roles in the organization of the lymphoid tissues and the development of lymphoid malignancies. We investigated the expression of these CKs and their receptors in the salivary glands of Sjogren's syndrome patients with lymphoepithelial lesions (lymphoepithelial sialadenitis or LESA) and in MALT lymphoma to understand their involvement in salivary gland lymphomagenesis. We demonstrate that within salivary glands with LESA and MALT lymphoma the lymphoid CKs CXCL13 and CCL21 are selectively associated with areas of reactive lymphoid proliferation, whereas no significant expression of these molecules was detected in the malignant lymphoid aggregate. Conversely, CXCL12 was observed predominantly in infiltrated ducts and malignant B cells. Accordingly, CXCL13 and CCL21 transcript levels were significantly increased in LESA samples while CXCL12 levels were increased in MALT lymphoma and isolated tumor cells. Low levels of CK receptors were detected on lymphoma-extracted lymphocytes, suggesting down-regulation in the abundance of ligands. Our findings suggest that in salivary gland MALT lymphoma the lymphoid CKs CXCL13 and CCL21 are directly implicated in the organization of ectopic reactive lymphoid tissue, whereas CXCL12 is associated with the infiltrated epithelium and malignant B cell component and is possibly involved in the regulation of malignant B cell survival.
机译:已知趋化因子(CK)CXCL13,CCL21和CXCL12在淋巴组织的组织和淋巴恶性肿瘤的发展中起着不同的作用。我们调查了这些CK及其受体在患有淋巴上皮病变(淋巴管上皮性腺炎或LESA)的干燥综合征患者的唾液腺和MALT淋巴瘤中的表达,以了解它们参与唾液腺淋巴瘤的发生。我们证明在LESA和MALT淋巴瘤的唾液腺中,淋巴样CKs CXCL13和CCL21与反应性淋巴样增生区域选择性相关,而在恶性淋巴样聚集物中未检测到这些分子的显着表达。相反,CXCL12主要在浸润的导管和恶性B细胞中观察到。因此,LESA样品中的CXCL13和CCL21转录水平显着升高,而MALT淋巴瘤和分离的肿瘤细胞中CXCL12的水平升高。在淋巴瘤提取的淋巴细胞上检测到低水平的CK受体,表明配体的丰度下调。我们的发现表明,在唾液腺MALT淋巴瘤中,淋巴样CKs CXCL13和CCL21直接与异位反应性淋巴组织的组织有关,而CXCL12与浸润的上皮和恶性B细胞成分有关,可能与恶性B的调节有关。细胞存活。

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