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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Eotaxin (CCL11) and Eotaxin-2 (CCL24) Induce Recruitment of Eosinophils, Basophils, Neutrophils, and Macrophages As Well As Features of Early- and Late-Phase Allergic Reactions Following Cutaneous Injection in Human Atopic and Nonatopic Volunteers.
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Eotaxin (CCL11) and Eotaxin-2 (CCL24) Induce Recruitment of Eosinophils, Basophils, Neutrophils, and Macrophages As Well As Features of Early- and Late-Phase Allergic Reactions Following Cutaneous Injection in Human Atopic and Nonatopic Volunteers.

机译:嗜酸性粒细胞趋化因子(CCL11)和嗜酸性粒细胞趋化因子2(CCL24)诱导嗜酸性粒细胞,嗜碱性粒细胞,嗜中性粒细胞和巨噬细胞的募集,以及在人类特应性和非特应性志愿者皮肤性注射后早期和晚期过敏反应的特征。

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Eotaxin and eotaxin-2, acting through CCR3, are potent eosinophil chemoattractants both in vitro and in animal models. In this study we examined the capacity of eotaxin and eotaxin-2 to recruit eosinophils and other inflammatory cells in vivo in human atopic and nonatopic skin. Skin biopsies taken after intradermal injection of eotaxin and eotaxin-2 were examined by immunohistochemistry. Allergen- and diluent-challenged sites were used as positive and negative controls. Eotaxin and eotaxin-2 produced a dose- and time-dependent local eosinophilia of comparable intensity in both atopic and nonatopic individuals. This was associated with an acute wheal and flare response at the site of injection and development of a cutaneous late phase reaction in a proportion of subjects. There was an accompanying decrease in mast cell numbers. Both chemokines also induced the accumulation of basophils and an unexpected early infiltration of neutrophils. Macrophages were prominent at the 24-h point. Although there was surface CCR3 expression on neutrophils in whole blood, we were unable to demonstrate any functional neutrophil responses to eotaxin in vitro. Thus, intradermal injection of eotaxin and eotaxin-2 in humans induced infiltration of eosinophils and other inflammatory cells as well as changes consistent with CC chemokine-induced mast cell degranulation.
机译:通过CCR3起作用的嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2在体外和动物模型中都是有效的嗜酸性粒细胞趋化因子。在这项研究中,我们检查了嗜酸性粒细胞和嗜酸性粒细胞趋化因子2在人体特应性和非特应性皮肤中募集嗜酸性粒细胞和其他炎症细胞的能力。皮内注射eotaxin和eotaxin-2后进行的皮肤活检通过免疫组织化学检查。变应原和稀释剂攻击的位点用作阳性和阴性对照。嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2在特应性和非特应性个体中产生的剂量和时间依赖性的局部嗜酸性粒细胞增生程度相当。这与一定比例的受试者在注射部位的剧烈的皮疹和耀斑反应以及皮肤后期反应的发展有关。肥大细胞数量随之减少。两种趋化因子还诱导嗜碱性粒细胞的积累和中性粒细胞的意外早期浸润。巨噬细胞在24小时内突出。尽管全血中性粒细胞表面有CCR3表达,但我们无法在体外证明任何功能性中性粒细胞对嗜酸性粒细胞趋化因子的反应。因此,在人体内皮内注射嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2诱导嗜酸性粒细胞和其他炎性细胞的浸润以及与CC趋化因子诱导的肥大细胞脱粒相一致的变化。

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