Rothenberg M E, Mishra A, Brandt E B, Hogan S P
Department of Pediatrics, Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA.
Immunol Rev. 2001 Feb;179:139-55. doi: 10.1034/j.1600-065x.2001.790114.x.
The gut-associated lymphoid tissue (GALT) is composed of lymphocytes residing in Peyer's patches, lamina propria, and intraepithelial compartments. In addition to these features which distinguish GALT from other peripheral sites of the immune system, the gastrointestinal immune system is also composed of resident eosinophils. Eosinophils are generally considered to be peripheral blood leukocytes that have an important pro-inflammatory role in various immune disorders. Although most research concerning this cell has focused on understanding its trafficking and function in the blood and lung, recent studies have also started to elucidate its regulation and function in the gastrointestinal tract. Interestingly, eosinophil numbers in the gastrointestinal tract are substantially higher than in other tissues. At baseline (healthy conditions), most eosinophils reside in the lamina propria in the stomach and intestine. Eosinophil homing to these sites occurs during embryonic development and their levels in perinatal mice are comparable to those in adults, indicating that their homing is not dependent upon the presence of intestinal flora. Furthermore, eosinophil localization to the lamina propria at baseline is critically regulated by eotaxin, a chemokine constitutively expressed throughout the gastrointestinal tract. Although eotaxin is required for eosinophil homing, its expression in the esophagus is not sufficient for eosinophil accumulation, since this organ is devoid of eosinophils at baseline. During Th2-associated inflammatory conditions (e.g. interleukin (IL)-5 overexpression or oral allergen challenge), marked increases of eosinophils occur not only in the lamina propria but also in Peyer's patches. The accumulation of Peyer's patch eosinophils, which mainly occurs in the outer cortex and interfollicular regions, is critically regulated by IL-5 and less significantly by eotaxin, suggesting the involvement of other eosinophil chemokines in this lymphoid compartment. Preliminary investigations have shown that gastrointestinal eosinophils express the alpha4beta7 integrin and that this molecule is responsible, in part, for eosinophil homing. In summary, eosinophils are resident cells of the gastrointestinal immune system whose levels can be induced by antigen exposure under Th2 conditions, in a manner that is critically regulated by eotaxin and IL-5. We propose that eosinophils are integral members of the gastrointestinal immune system and are likely to be important in innate, regulatory and inflammatory immune responses.
肠道相关淋巴组织(GALT)由位于派尔集合淋巴结、固有层和上皮内区室的淋巴细胞组成。除了这些将GALT与免疫系统其他外周部位区分开来的特征外,胃肠道免疫系统还由驻留的嗜酸性粒细胞组成。嗜酸性粒细胞通常被认为是外周血白细胞,在各种免疫紊乱中具有重要的促炎作用。尽管关于这种细胞的大多数研究都集中在了解其在血液和肺部的运输及功能,但最近的研究也开始阐明其在胃肠道中的调节和功能。有趣的是,胃肠道中的嗜酸性粒细胞数量明显高于其他组织。在基线状态(健康状况)下,大多数嗜酸性粒细胞驻留在胃和肠道的固有层中。嗜酸性粒细胞归巢到这些部位发生在胚胎发育期间,围产期小鼠体内的嗜酸性粒细胞水平与成年小鼠相当,这表明它们的归巢不依赖于肠道菌群的存在。此外,嗜酸性粒细胞在基线时定位于固有层受到嗜酸性粒细胞趋化因子的严格调控,嗜酸性粒细胞趋化因子是一种在整个胃肠道中组成性表达的趋化因子。尽管嗜酸性粒细胞趋化因子是嗜酸性粒细胞归巢所必需的,但其在食管中的表达不足以导致嗜酸性粒细胞积聚,因为在基线时该器官没有嗜酸性粒细胞。在与Th2相关的炎症状态下(例如白细胞介素(IL)-5过表达或口服过敏原激发),嗜酸性粒细胞不仅在固有层中显著增加,在派尔集合淋巴结中也显著增加。派尔集合淋巴结嗜酸性粒细胞的积聚主要发生在外皮质和滤泡间区域,受到IL-5的严格调控,而嗜酸性粒细胞趋化因子的调控作用较小,这表明其他嗜酸性粒细胞趋化因子参与了这个淋巴区室的调节。初步研究表明,胃肠道嗜酸性粒细胞表达α4β7整合素,并且该分子部分负责嗜酸性粒细胞的归巢。总之,嗜酸性粒细胞是胃肠道免疫系统的驻留细胞,其水平可在Th2条件下通过抗原暴露诱导,且受到嗜酸性粒细胞趋化因子和IL-5的严格调控。我们认为嗜酸性粒细胞是胃肠道免疫系统的重要组成部分,可能在固有免疫、调节性免疫和炎症免疫反应中发挥重要作用。