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Calcineurin Inhibitor in Autoimmune Enteropathy Management

机译:钙碱抑制剂在自身免疫肠病管理中

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Autoimmune enteropathy (AIE) is an entity reported primarily in infancy, resulting in intractable diarrhoea and associated with small bowel villous atrophy and the presence of circulating anti-enterocyte antibodies. It is a multisystem disorder with a response, in many cases, to immunosuppressive therapy. However, small bowel enteropathies that are associated with an autoimmune process are often resistant to initial treatment. Cyclosporine is a well known calcineurin inhibitor and potent immunosuppressive drug mostly used in organ transplantation. Since the mid-1980s, this drug is also being used to treat patients with inflammatory bowel diseases. At this time, cyclosporine is most useful in severely ill patients with ulcerative colitis, who have not responded to corticosteroid therapy. In such patients, intravenously administered cyclosporine may be highly effective for rapid disease control, thus changing a risky emergency situation into a less urgent procedure. However, cyclosporine is lipid-bound and may be associated with an increased risk of seizures when it is administered to acutely ill, severely malnourished patients with mal lipid absorption. The drug has a significant side effect profile that includes renal insufficiency and hypertension in some individuals. Therefore, therapeutic drug monitoring (TDM) is required for dosing of the drug to optimize immunosuppressive efficacy, while minimizing its side effects. Some data also indicate a correlation between trough concentrations and area under the curve (AUC), whereas others recommend 2 hours post dose (C_2) drug concentration monitoring. The objective of the present paper is to demonstrate case model of effective outcomes of autoimmune entreopathy after therapeutic drug-monitoring guided calcineurin inhibitor, cyclosporine-A (CSA) therapy in a paediatric patient. The paper also discusses the new insights on mechanisms of action of calcineuin to control autoimmune diseases in general and autoimmune bowel diseases in particular.
机译:自身免疫肠病(AIE)是主要在婴儿期报告的实体,导致顽固性腹泻和与小肠绒毛萎缩和循环抗肠细胞抗体的存在相关。它是一种多系统障碍,在许多情况下,对免疫抑制治疗的反应。然而,与自身免疫过程相关的小肠肠病通常耐受初始治疗。环孢菌素是众所周知的煅烧酶抑制剂和有效的免疫抑制药,主要用于器官移植。自20世纪80年代中期以来,该药物也用于治疗炎症性肠病患者。此时,环孢菌素在严重生病的溃疡性结肠炎患者中最有用,患者没有反应皮质类固醇治疗。在这些患者中,静脉内给药的环孢菌素对于快速疾病控制可能是非常有效的,因此将危险的紧急情况变为较少的紧急程序。然而,环孢菌素是脂质结合的,并且当缉获到急性病,严重营养不良的患者的癫痫发芽患者的癫痫发作的风险增加时,可能与脂肪吸收的患者增加。该药物具有重要的副作用曲线,包括一些人的肾功能不全和高血压。因此,治疗药物监测(TDM)是给药药物以优化免疫抑制功效,同时最小化其副作用。一些数据还表明曲线下的槽浓度和面积之间的相关性,而其他数据则推荐2小时后剂量(C_2)药物浓度监测。本文的目的是展示治疗药物监测引导式钙蛋白抑制剂,儿科患者中的环孢菌素-A(CSA)治疗后自身免疫性疗效的有效结果的案例模型。本文还探讨了钙铝的作用机制的新见解,特别是对一般和自身免疫性肠道疾病进行自身免疫疾病。

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