Can eculizumab be an option in traditional treatment-resistant ulcerative colitis?

Hakan Ozer, İsmail Baloglu, Kultigin Turkmen, Halil Zeki Tonbul, Nedim Yılmaz Selcuk
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Abstract

Atypical/complement-mediated hemolytic uremic syndrome (A-HUS/CM-HUS) is a hereditary or sporadic disease with thrombotic microangiopathy (TMA). Diarrhea is a trigger that can cause attacks of CM-HUS. Although there are opinions that complement system activation plays a role in intestinal inflammation in patients with inflammatory bowel disease, the association of TMA with inflammatory bowel disease (IBD) has rarely been reported. In our case, a CM-HUS case that developed without an additional triggering factor in the course of ulcerative colitis (UC) was successfully treated with eculizumab, and then UC remission was also achieved. In this context, we would like to point out that the irregularities in the alternative pathway of the complement system may cause clinical findings in extra-renal organs, and the complement system may also play a role in the pathogenesis of inflammatory bowel disease. In addition, we think that our case may guide further studies on the usability of anti-complement therapies in treating patients with IBD who are resistant to conventional treatments.

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依库珠单抗能否成为传统治疗耐药溃疡性结肠炎的一种选择?
非典型/补体介导的溶血性尿毒症综合征(A-HUS/CM-HUS)是一种伴有血栓性微血管病(TMA)的遗传性或散发性疾病。腹泻是导致 CM-HUS 发作的一个诱因。虽然有观点认为补体系统激活在炎症性肠病患者的肠道炎症中起作用,但 TMA 与炎症性肠病(IBD)相关的报道却很少。在我们的病例中,一例在溃疡性结肠炎(UC)病程中没有额外诱发因素的 CM-HUS 成功接受了依库珠单抗治疗,随后 UC 也得到了缓解。在此,我们想指出的是,补体系统替代途径的不规则性可能会导致肾外器官出现临床症状,补体系统也可能在炎症性肠病的发病机制中发挥作用。此外,我们认为我们的病例可能会指导进一步的研究,探讨抗补体疗法在治疗对常规疗法产生抗药性的 IBD 患者方面的可用性。
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