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首页> 外文期刊>BMC Gastroenterology >Treatment of children and adolescents with ulcerative colitis by adsorptive depletion of myeloid lineage leucocytes as monotherapy or in combination with low dose prednisolone after failure of first-line medications
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Treatment of children and adolescents with ulcerative colitis by adsorptive depletion of myeloid lineage leucocytes as monotherapy or in combination with low dose prednisolone after failure of first-line medications

机译:一线药物治疗失败后,通过单核或与小剂量泼尼松龙联用,吸收性吸收髓系谱系白细胞治疗溃疡性结肠炎儿童和青少年

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Background Currently available drugs for the treatment of ulcerative colitis (UC) include salicylates, thiopurines, corticosteroids and new anti-tumour necrosis factor (TNF)-α biologics. Among these medications, corticosteroids in children and adolescents may adversely affect the patients’ growth and development. Further, UC patients have elevated and activated myeloid lineage leucocytes including the CD14?+?CD16+ monocytes, which release TNF-α as a significant exacerbating factor. Accordingly, depletion of these cells by granulocyte/monocyte adsorption (GMA) should alleviate inflammation and promote UC remission. The objective of this study was to evaluate the efficacy of GMA in children and adolescents in whom conventional first-line medications had failed to induce remission. Methods In a single centre setting, between 2007 and 2012, a total of 24 consecutive children and adolescents, age 11–19 years were given mesalazine or sulphasalazine as a first-line medication. Seventeen patients relapsed or did not respond to the first-line medications, and received GMA with the Adacolumn, 2 sessions in the first week, and then weekly, up to 11 sessions. Patients who achieved a decrease of ≥5 in the clinical activity index (CAI) were to continue with GMA, while non-responders were to receive 0.5 to 1.0 mg/kg/day prednisolone (PSL) plus additional GMA sessions similar to GMA responder cases. At entry and week 12, patients were clinically and endoscopically evaluated, allowing each patient to serve as her/his own control. Results Seven patients achieved remission with the first-line medications and did not receive GMA. Five patients did not respond to the first 5 GMA sessions and received PSL plus GMA, while 12 patients responded to the first 5 GMA sessions and received additional sessions. At entry, the average CAI was 12.7?±?2.5, range 8–17, and the average endoscopic index was 8.5?±?1.5, range 7–11. The corresponding values at week 12 were 2.1?±?0.2, range 1–4 (P? Conclusions With the strategy we applied in this study, all 24 consecutive patients achieved remission. In growing patients with active UC refractory to first-line medications, GMA was associated with clinical remission and mucosal healing, while in non-responders to GMA monotherapy, addition of a low dose PSL enhanced the efficacy of GMA and tapering of the PSL dose soon after remission was not associated with UC relapse. Therefore, the majority of young corticosteroid naive UC patients in whom first-line salicylates have failed may respond to GMA and be spared from additional drug therapy. Avoiding corticosteroids at an early stage of UC should ensure better long-term clinical course.
机译:背景技术当前可用于治疗溃疡性结肠炎(UC)的药物包括水杨酸盐,硫代嘌呤,皮质类固醇和新型抗肿瘤坏死因子(TNF)-α生物制剂。在这些药物中,儿童和青少年的皮质类固醇可能会对患者的生长发育产生不利影响。此外,UC患者的髓系谱系白细胞升高并被激活,包括CD14β+βCD16+单核细胞,它们释放出TNF-α作为重要的恶化因素。因此,粒细胞/单核细胞吸附(GMA)消耗这些细胞应减轻炎症并促进UC缓解。这项研究的目的是评估GMA在常规一线药物未能诱导缓解的儿童和青少年中的疗效。方法在2007年至2012年的单一中心环境中,连续对24名11-19岁的儿童和青少年连续给予美沙拉嗪或柳氮磺吡啶作为一线药物。 17名患者复发或对一线药物没有反应,并与Adacolumn一起接受GMA治疗,第一周共2次,然后每周一次,共11次。临床活动指数(CAI)下降≥5的患者将继续接受GMA治疗,而无反应者应接受0.5至1.0 mg / kg /天的泼尼松龙(PSL)以及与GMA反应者相似的其他GMA疗程。在入院和第12周时,对患者进行了临床和内窥镜评估,使每位患者都可以作为自己的对照。结果7例患者通过一线药物获得缓解,未接受GMA治疗。五名患者对前5个GMA疗程无反应,接受了PSL加GMA,而12例患者对前5个GMA疗程有反应,并接受了其他疗程。进入时,平均CAI为12.7±2.5,范围为8-17,平均内窥镜指数为8.5±1.5,范围为7-11。在第12周时的相应值为2.1±0.2,范围为1-4(P?结论)采用本研究策略后,连续24例患者均获得了缓解。在成长中的一线药物难以治疗的活动性UC患者中, GMA与临床缓解和粘膜愈合相关,而在对GMA单药无效的患者中,添加低剂量PSL可以增强GMA的疗效,并且缓解后不久逐渐减少PSL剂量与UC复发无关。一线水杨酸盐治疗失败的年轻皮质类固醇初治UC患者可能对GMA有反应,可以避免其他药物治疗,在UC早期避免使用皮质类固醇应确保更好的长期临床过程。

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