派尔集合淋巴结嗜酸性粒细胞:黏膜变应原暴露、白细胞介素-5和嗜酸性粒细胞趋化因子对其的识别、表征及调控
Peyer's patch eosinophils: identification, characterization, and regulation by mucosal allergen exposure, interleukin-5, and eotaxin.
作者信息
Mishra A, Hogan S P, Brandt E B, Rothenberg M E
机构信息
Division of Pulmonary Medicine, Allergy and Clinical Immunology, Department of Pediatrics, Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
出版信息
Blood. 2000 Aug 15;96(4):1538-44.
The gastrointestinal immune system is traditionally thought to be composed of lymphocytes located within Peyer's patches and the lamina propria. We have recently reported that eosinophils also reside in the gastrointestinal tract during healthy states, in particular, within the lamina propria, and that these cells substantially increase after oral allergen exposure. We now demonstrate the presence of eosinophils in Peyer's patches and characterize the signals that regulate the accumulation of eosinophils in Peyer's patches. In contrast to the lamina propria, intestinal Peyer's patches have very low levels of eosinophils under healthy states. However, elevated levels of interleukin-5 (IL-5), generated by transgenic or pharmacologic approaches, result in a dramatic increase in eosinophil levels in Peyer's patches. Most eosinophils are located in the outer cortex and interfollicular regions of the Peyer's patches. To dissect the mechanism of eosinophil trafficking to Peyer's patches, the role of eotaxin was examined. Mice transgenic for IL-5 and genetically deficient in eotaxin were found to have reduced levels of eosinophils in Peyer's patches compared with IL-5-transgenic mice. To prove that eosinophils also traffic to Peyer's patches in wild-type mice, allergic hypersensitivity was induced and Peyer's patches were examined. Exposure to mucosal allergen promoted marked accumulation of eosinophils in Peyer's patches and this process was attenuated in eotaxin-deficient mice. In summary, these data demonstrate that elevated levels of IL-5 and mucosal allergen exposure promote eotaxin-dependent eosinophil trafficking to Peyer's patches. These studies suggest that eosinophils may cooperate with lymphocytes in the development of mucosal immune responses in the gastrointestinal tract. (Blood. 2000;96:1538-1544)
传统观点认为,胃肠道免疫系统由派尔集合淋巴结和固有层中的淋巴细胞组成。我们最近报道,在健康状态下,嗜酸性粒细胞也存在于胃肠道中,尤其是固有层内,并且在口服过敏原暴露后这些细胞会大量增加。我们现在证明派尔集合淋巴结中存在嗜酸性粒细胞,并对调节嗜酸性粒细胞在派尔集合淋巴结中聚集的信号进行了表征。与固有层不同,在健康状态下,肠道派尔集合淋巴结中的嗜酸性粒细胞水平非常低。然而,通过转基因或药理学方法产生的白细胞介素-5(IL-5)水平升高,会导致派尔集合淋巴结中嗜酸性粒细胞水平急剧增加。大多数嗜酸性粒细胞位于派尔集合淋巴结的外层皮质和滤泡间区域。为了剖析嗜酸性粒细胞向派尔集合淋巴结迁移的机制,我们研究了嗜酸性粒细胞趋化因子的作用。发现IL-5转基因且嗜酸性粒细胞趋化因子基因缺陷的小鼠与IL-5转基因小鼠相比,派尔集合淋巴结中的嗜酸性粒细胞水平降低。为了证明野生型小鼠中的嗜酸性粒细胞也会迁移到派尔集合淋巴结,我们诱导了过敏性超敏反应并检查了派尔集合淋巴结。暴露于黏膜过敏原会促进派尔集合淋巴结中嗜酸性粒细胞的显著聚集,而在嗜酸性粒细胞趋化因子缺陷的小鼠中,这一过程会减弱。总之,这些数据表明,IL-5水平升高和黏膜过敏原暴露会促进嗜酸性粒细胞趋化因子依赖性嗜酸性粒细胞向派尔集合淋巴结的迁移。这些研究表明,嗜酸性粒细胞可能在胃肠道黏膜免疫反应的发展中与淋巴细胞协同作用。(《血液》。2000年;96:1538 - 1544)