Davenport Mark
Department of Paediatric Surgery, King's College Hospital, London, SE5 9RS, UK.
Pediatr Surg Int. 2017 Dec;33(12):1263-1273. doi: 10.1007/s00383-017-4157-5. Epub 2017 Sep 22.
Given that the aetiology of biliary atresia (BA) is complex and that there is a multiplicity of possible pathogenic mechanisms then it is perhaps not surprising that the evidence for effect of a number of different agents is contradictory. Post-operative cholangitis for instance is common, bacterial in origin and various antibiotic regimens have been tested (although none in a randomized trial) but continuation beyond the early post-operative period does not appear to offer any greater protection. There is an inflammatory reaction in about 25-35% of cases of BA illustrated by abnormal expression of class II antigen and upregulation of ICAM, VCAM and E-selectin with an infiltrate of immune-activated T cells (predominantly CD4 + Th1 and Th17) and NK cells and a systemic surge in inflammatory cytokines (e.g. TNF-α, IL-2, IL-12). This has potential as a therapeutic target and is the main hypothesis behind the rationale use of steroids. The first report of steroids was published in 1985 by Karrer and Lilly as "blast" therapy to treat recalcitrant cholangitis, followed by a multiplicity of small-scale uncontrolled studies suggesting benefit. To date there has been one randomized placebo-controlled study with a low-dose (prednisolone 2 mg/kg/day) regimen (2007); one with a high-dose (IV prednisolone 4 mg/kg/day regimen) (2014); two prospective high-dose open-label studies (2013); a prospective comparison of low- and high-dose regimen and a large (380 infants) retrospective comparison. The most recent meta-analysis (2016) identified a significant difference in clearance of jaundice at 6 months (OR 1.59, 95% CI 1.03-2.45, P = 0.04), in patients treated with high-dose steroids, particularly if < 70 days at surgery. Ursodeoxycholic acid (UDCA) may increase choleresis or change the ratio of endogenous bile acids to a less hydrophobic and, therefore, less toxic millieu. UDCA may protect cholangiocyte membranes against damage and perhaps reduce the tendency to fibrogenesis. Biochemical benefit has been shown in a single crossover trial in older BA children who had cleared their jaundice. Other potential adjuvant therapies include immunoglobulin therapy, anti-viral agents and Chinese herbs although real evidence of benefit is lacking.
鉴于胆道闭锁(BA)的病因复杂,且存在多种可能的致病机制,那么许多不同因素作用的证据相互矛盾或许就不足为奇了。例如,术后胆管炎很常见,其源于细菌感染,人们已对各种抗生素治疗方案进行了测试(尽管均未进行随机试验),但术后早期之后继续使用抗生素似乎并不能提供更大的保护。约25% - 35%的BA病例存在炎症反应,表现为II类抗原异常表达、细胞间黏附分子(ICAM)、血管细胞黏附分子(VCAM)和E - 选择素上调,伴有免疫激活的T细胞(主要是CD4 + Th1和Th17)和NK细胞浸润以及炎症细胞因子(如肿瘤坏死因子 - α、白细胞介素 - 2、白细胞介素 - 12)的全身激增。这具有作为治疗靶点的潜力,也是合理使用类固醇的主要假设依据。1985年,卡勒和利利首次发表了关于类固醇作为“冲击”疗法治疗顽固性胆管炎的报告,随后有多项小规模非对照研究表明其有益。迄今为止,有一项关于低剂量(泼尼松龙2毫克/千克/天)方案的随机安慰剂对照研究(2007年);一项关于高剂量(静脉注射泼尼松龙4毫克/千克/天方案)的研究(2014年);两项前瞻性高剂量开放标签研究(2013年);一项低剂量和高剂量方案的前瞻性比较以及一项大型(380名婴儿)回顾性比较。最近的荟萃分析(2016年)发现,接受高剂量类固醇治疗的患者在6个月时黄疸清除率存在显著差异(比值比1.59,95%置信区间1.03 - 2.45,P = 0.04),尤其是手术时年龄小于70天的患者。熊去氧胆酸(UDCA)可能会增加胆汁分泌或改变内源性胆汁酸的比例,使其变为疏水性较低、毒性也较低的环境。UDCA可能保护胆管细胞膜免受损伤,并可能降低纤维化的倾向。在一项针对已清除黄疸的大龄BA儿童的单交叉试验中已显示出生化益处。其他潜在的辅助治疗包括免疫球蛋白治疗、抗病毒药物和中药,不过目前尚缺乏实际的有益证据。