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MHC class II expression by Langerhans cells and lymph node dendritic cells: possible evidence for maturation of Langerhans cells following contact sensitization.

机译:朗格汉斯细胞和淋巴结树突状细胞表达的MHC II类:接触致敏后朗格汉斯细胞成熟的可能证据。

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摘要

Following exposure of mice to contact sensitizing chemicals, dendritic cells (DC) rapidly accumulate in the draining lymph nodes. A proportion, at least, of the DC which arrive in the nodes bear significant amounts of antigen and are derived from epidermal Langerhans' cells (LC). It is of interest that although LC are relatively inefficient antigen-presenting cells, the antigen-bearing DC found within draining nodes are potent accessory cells and induce immune responses both in vitro and in vivo. Previous in vitro studies have shown that during culture in the presence of granulocyte/macrophage colony-stimulating factor (GM-CSF), LC are subject to a functional and phenotypic maturation characterized by the development of effective accessory cell function and elevated membrane Ia antigen expression. We have hypothesized previously that LC may undergo a similar maturation in vivo as they move to the draining lymph nodes following receipt of the stimulus to migrate. As maturation in vitro is accompanied by increased Ia, we have examined the expression of this molecule on epidermal LC and lymph node DC during the induction phase of contact sensitization. The data reported provide evidence that peripheral lymph node DC, irrespective of whether they are derived from draining or resting nodes, and irrespective of whether or not they bear antigen, express comparable high levels of Ia antigen. In contrast, compared with DC, freshly isolated LC have considerably less (on average five times less) Ia antigen. These results indicate that during migration from the skin to lymphoid tissue LC are subject to a phenotypic maturation, comparable with that observed in vitro, and consistent with the acquisition of active antigen-presenting cell function.
机译:小鼠接触致敏化学物质后,树突状细胞(DC)迅速积聚在引流的淋巴结中。至少有一部分到达淋巴结的DC带有大量抗原,这些抗原来自表皮朗格汉斯细胞(LC)。令人感兴趣的是,尽管LC是相对低效率的抗原呈递细胞,但在引流节点内发现的带有抗原的DC是有效的辅助细胞,并在体外和体内诱导免疫应答。先前的体外研究表明,在存在粒细胞/巨噬细胞集落刺激因子(GM-CSF)的培养过程中,LC受到功能和表型的成熟,其特征在于有效辅助细胞功能的发展和膜Ia抗原表达的提高。先前我们假设,LC在接受刺激迁移后移至引流淋巴结时可能会在体内经历类似的成熟。由于体外成熟伴随着Ia的增加,因此我们已经研究了在接触致敏诱导阶段该分子在表皮LC和淋巴结DC上的表达。报道的数据提供了证据,即外周淋巴结DC,无论它们是来自引流还是静息淋巴结,无论它们是否携带抗原,都表达相当高水平的Ia抗原。相反,与DC相比,新鲜分离的LC的Ia抗原要少得多(平均少5倍)。这些结果表明,在从皮肤向淋巴组织的迁移过程中,LC发生了表型成熟,与体外观察到的情况相当,并且与活性抗原呈递细胞功能的获得相一致。

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