亚急性坏死性淋巴结炎的髓过氧化物酶阳性组织细胞表达CD11c和CD163

Seon Jung Jang, Hyae Min Jeon, Dowhan Kim, Woo-Ick Yang
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引用次数: 2

摘要

背景和目的:亚急性坏死性淋巴结炎(SNL)的病变组织细胞免疫表型分析揭示了一些意想不到的发现。组织细胞表达髓过氧化物酶(MPO),未成熟树突状细胞占SNL病变细胞的很大比例。然而,表达mpo的SNL病变组织细胞是否也表达未成熟树突状细胞的免疫表型标志物尚未确定。方法:采用树突状细胞和巨噬细胞标记物对26例SNL患者石蜡包埋组织切片中病变组织细胞的免疫表型进行分析。双免疫组化染色也证实了几种标记物的共表达。结果:表达cd11c的组织细胞占病变细胞的主要组成部分(平均占病变面积的50.1%),超过cd163阳性的组织细胞(平均占病变面积的32.0%)。双重免疫组化染色证实,大量表达cd11c的组织细胞也共表达MPO和CD163。cd123阳性浆细胞样树突状细胞(平均占病变面积的3.2%)为次要病变细胞,而筋膜蛋白阳性的成熟树突状细胞在病变中不存在。结论:我们的研究结果表明,SNL的主要病变细胞是表达骨髓树突状细胞和巨噬细胞标记物以及MPO的组织细胞,表明组织细胞谱系细胞具有表型可塑性和功能多功能性。
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Myeloperoxidase positive histiocytes in subacute necrotizing lymphadenitis express both CD11c and CD163

Background and aim: Immunophenotype analysis of lesional histiocytes in subacute necrotizing lymphadenitis (SNL) has revealed several unexpected findings. Histiocytes express myeloperoxidase (MPO), and immature dendritic cells occupy a significant proportion of the lesional cells in SNL. However, whether MPO-expressing lesional histiocytes of SNL also express immunophenotypic markers of immature dendritic cells has not been determined. Methods: The immunophenotypes of lesional histiocytes in paraffin-embedded tissue sections from 26 patients with SNL were analyzed using a panel of dendritic cell and macrophage markers. Double immunohistochemical staining was also performed to confirm coexpression of several markers. Results: CD11c-expressing histiocytes represented a major component of lesional cells (averaging 50.1% of the lesional area), surpassing CD163-positive histiocytes (averaging 32.0% of the lesional area). Double immunohistochemical staining confirmed that a significant proportion of CD11c-expressing histiocytes also coexpressed MPO as well as CD163. CD123-positive plasmacytoid dendritic cells (averaging 3.2% of the lesional area) were minor lesional cells, and fascin-positive mature dendritic cells were not present in the lesions. Conclusions: Our results demonstrate that the main lesional cells in SNL are histiocytes expressing myeloid dendritic cell and macrophage markers as well as MPO, indicating phenotypic plasticity and functional versatility of histiocyte lineage cells.

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