首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Recruitment of immature plasmacytoid dendritic cells (plasmacytoid monocytes) and myeloid dendritic cells in primary cutaneous melanomas.
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Recruitment of immature plasmacytoid dendritic cells (plasmacytoid monocytes) and myeloid dendritic cells in primary cutaneous melanomas.

机译:在原发性皮肤黑素瘤中招募未成熟的浆细胞样树突状细胞(浆细胞样单核细胞)和髓样树突状细胞。

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摘要

The present study has analysed the distribution and phenotype of dendritic cells (DCs) in primary cutaneous melanomas and sentinel lymph nodes by immunohistochemistry. In primary melanomas, an increase of DCs was found in the epidermis and the peritumoural area. Intraepidermal DCs were mostly CD1a(+)/Langerin(+) Langerhans cells. Peritumoural DCs included a large population of DC-SIGN(+)/mannose-receptor(+)/CD1a(-) DCs, a small subset of CD1a(+) DCs, and, remarkably, plasmacytoid monocytes/plasmacytoid DCs (PM/PDCs). The PM/PDCs, most likely recruited by SDF-1 secreted by melanoma cells, produced type I interferon (IFN-I), but the expression of the IFN-alpha inducible protein MxA was extremely variable and very limited in the majority of cases. All DC subsets were predominantly immature. The peritumoural area also contained a minor subset of mature CD1a(+) DCs. However, the small amount of local interleukin (IL)-12 p40 mRNA and the naive phenotype of 20-50% of peritumoural T-lymphocytes are consistent with poor T-cell stimulation or erroneous recruitment. In sentinel lymph nodes, notable expansion of mature CD1a(+)/Langerin(+) DCs was observed. The paucity of intratumoural DCs and the predominant immature phenotype of peritumoural dermal DCs indicate defective maturation of primary cutaneous melanoma-associated DCs, resulting in lack of T-cell priming. These results may explain why melanoma cells grow despite the presence of infiltrating immune cells.
机译:本研究通过免疫组织化学分析了原发性皮肤黑素瘤和前哨淋巴结中树突状细胞(DC)的分布和表型。在原发性黑色素瘤中,在表皮和肿瘤周围区域发现DC升高。表皮内DCs主要是CD1a(+)/ Langerin(+)Langerhans细胞。周围性DC包括大量DC-SIGN(+)/甘露糖受体(+)/ CD1a(-)DC,一小部分CD1a(+)DC,以及明显的浆细胞样单核细胞/浆细胞样DC(PM / PDC) )。 PM / PDC最有可能是由黑色素瘤细胞分泌的SDF-1募集的,产生了I型干扰素(IFN-I),但是在大多数情况下,IFN-α诱导蛋白MxA的表达变化很大,而且非常有限。所有DC子集主要是不成熟的。肿瘤周围区域还包含少量的成熟CD1a(+)DC。然而,少量的局部白介素(IL)-12 p40 mRNA和肿瘤周围T淋巴细胞的20-50%的幼稚表型与不良的T细胞刺激或错误募集相符。在前哨淋巴结中,观察到成熟的CD1a(+)/ Langerin(+)DC的显着扩展。肿瘤内DC的缺乏和肿瘤周围皮肤DC的主要未成熟表型表明原发性皮肤黑素瘤相关DC的成熟缺陷,导致缺乏T细胞启动。这些结果可以解释为什么尽管存在浸润性免疫细胞,黑素瘤细胞仍生长。

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