首页> 外文期刊>Experimental and therapeutic medicine >Pediatric patients with inflammatory bowel disease exhibit increased serum levels of proinflammatory cytokines and chemokines, but decreased circulating levels of macrophage inhibitory protein-1 beta, interleukin-2 and interleukin-17
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Pediatric patients with inflammatory bowel disease exhibit increased serum levels of proinflammatory cytokines and chemokines, but decreased circulating levels of macrophage inhibitory protein-1 beta, interleukin-2 and interleukin-17

机译:小儿炎症性肠病患者的血清促炎细胞因子和趋化因子水平升高,但巨噬细胞抑制蛋白1β,白介素2和白介素17的循环水平降低

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摘要

Inflammatory bowel disease (IBD) is a chronic and progressive inflammatory condition of the gastrointestinal tract. Although the causative events that lead to the onset of IBD are yet to be fully elucidated, deregulation of immune and inflammatory mechanisms are hypothesized to significantly contribute to this disorder. Since the onset of IBD is often during infancy, in the present study, the serum values of a large panel of cytokines and chemokines in pediatric patients (<18 years; n=26) were compared with age-matched controls (n=37). While elevations in the serum level of several proinflammatory and immune regulating cytokines were confirmed, such as interleukin (IL)-1 beta, IL-5, IL-7, interferon (IFN)-gamma-inducible protein-10, IL-16, cutaneous T-cell-attracting chemokine, leukemia inhibitory factor, monokine induced by gamma-IFN, IFN-alpha 2 and IFN-gamma, notably decreased levels of IL-2, IL-17 and macrophage inhibitory protein-1 beta were also observed. Therefore, while a number of proinflammatory cytokines exhibit increased levels in IBD patients, pediatric IBD patients may also exhibit certain aspects of a reduced immunological response.
机译:炎症性肠病(IBD)是胃肠道的一种慢性和进行性炎症。尽管导致IBD发作的病因尚未完全阐明,但据推测免疫和炎性机制的失调可明显导致这种疾病。由于IBD的发作通常在婴儿期,因此在本研究中,将小儿患者(<18岁; n = 26)中一大批细胞因子和趋化因子的血清值与年龄匹配的对照组(n = 37)进行了比较。 。虽然确认了几种促炎和免疫调节细胞因子的血清水平升高,例如白介素(IL)-1 beta,IL-5,IL-7,干扰素(IFN)-γ诱导型蛋白10,IL-16,还观察到皮肤T细胞吸引趋化因子,白血病抑制因子,γ-IFN,IFN-α2和IFN-γ诱导的单因子,IL-2,IL-17和巨噬细胞抑制蛋白-1β水平显着降低。因此,尽管许多促炎细胞因子在IBD患者中表现出升高的水平,但是儿科IBD患者也可能表现出免疫应答降低的某些方面。

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