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Fab抗体片段:在临床毒理学中的一些应用

Fab antibody fragments: some applications in clinical toxicology.

作者信息

Flanagan Robert J, Jones Alison L

机构信息

Medical Toxicology Unit, Guy's and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Drug Saf. 2004;27(14):1115-33. doi: 10.2165/00002018-200427140-00004.

Abstract

This review provides current information on the use of antigen-binding fragments (Fab) from cleaved antibodies to treat poisoning with digoxin and other potent, low formula mass poisons, such as colchicine and tricyclic antidepressants. Anti-digoxin Fab fragments have been used successfully for many years in the management of severe poisoning with digoxin, digitoxin, and a range of other structurally related compounds, including cardiotoxins from Nerium and Thevetia sp. (oleander) and Bufo sp. (toads). However, their main use remains treating digoxin poisoning. Equimolar doses of anti-digoxin Fab fragments completely bind digoxin in vivo. The approximate dose of Fab fragments (mg) is 80 times the digoxin body burden (mg). If neither the dose ingested nor the plasma digoxin/digitoxin concentration is known, in an adult 380 mg of anti-digoxin Fab fragments should be given. The dose for elderly patients or those with renal impairment should be similar to that for those with normal renal function. Fab fragments have a plasma half-life of 12-20 hours, but this can be prolonged in patients with renal impairment. Analysis of serum ultrafiltrate using an immunoassay shown not to have matrix bias remains the most accurate approach to measuring free digoxin in the presence of anti-digoxin Fab fragments. The antibody fragments are given intravenously over 15-30 minutes after dilution to at least 250 mL with plasma protein solution, 0.9% (w/v) sodium chloride, or deionised water, except in infants where the volume infused can be reduced. Factors limiting the efficacy of Fab fragments are the dose, the duration of the infusion and any delay in administration. Guidelines for Fab fragment administration in children include (i) dilution to a final Fab concentration of 10 g/L in either 5% (w/v) dextrose or 0.9% (w/v) sodium chloride; (ii) infusion through a 0.22 microm filter; (iii) administration of the total dose over a minimum of 30 minutes; and (iv) avoiding coadministration of other drugs and/or electrolyte solutions. Fab fragments are generally well tolerated. Adverse effects attributable to Fab treatment include hypokalaemia and exacerbation of congestive cardiac failure; renal function could be impaired in some patients. Fab fragment preparations for treating acute colchicine and tricyclic antidepressant poisoning have been developed, but are not available commercially. Colchicine poisoning is rare in Western countries, and pharmacological management together with supportive care is usually effective even in severe tricyclic antidepressant overdosage. Attempts have been made to produce anti-paraquat antibodies capable of enhancing paraquat elimination from the lung, but thus far all such attempts have proved unsuccessful.

摘要

本综述提供了有关使用经裂解抗体产生的抗原结合片段(Fab)治疗地高辛中毒以及秋水仙碱和三环类抗抑郁药等其他强效、低分子量毒物中毒的最新信息。多年来,抗地高辛Fab片段已成功用于治疗地高辛、洋地黄毒苷以及一系列其他结构相关化合物的严重中毒,包括夹竹桃属和黄花夹竹桃属植物(夹竹桃)以及蟾蜍属(蟾蜍)的心脏毒素。然而,它们的主要用途仍然是治疗地高辛中毒。等摩尔剂量的抗地高辛Fab片段可在体内完全结合地高辛。Fab片段的大致剂量(mg)是地高辛体内负荷(mg)的80倍。如果既不知道摄入剂量,也不知道血浆地高辛/洋地黄毒苷浓度,对于成年人应给予380mg抗地高辛Fab片段。老年患者或肾功能不全患者的剂量应与肾功能正常者相似。Fab片段的血浆半衰期为12 - 20小时,但在肾功能不全患者中可能会延长。使用显示无基质偏差的免疫测定法分析血清超滤液仍然是在存在抗地高辛Fab片段的情况下测量游离地高辛的最准确方法。抗体片段用血浆蛋白溶液、0.9%(w/v)氯化钠或去离子水稀释至至少250mL后,在15 - 30分钟内静脉注射,但婴儿的输注量可减少。限制Fab片段疗效的因素包括剂量、输注持续时间和给药延迟。儿童Fab片段给药指南包括:(i)在5%(w/v)葡萄糖或0.9%(w/v)氯化钠中稀释至最终Fab浓度为10g/L;(ii)通过0.22微米过滤器输注;(iii)在至少30分钟内给予总剂量;(iv)避免同时给予其他药物和/或电解质溶液。Fab片段一般耐受性良好。Fab治疗引起的不良反应包括低钾血症和充血性心力衰竭加重;一些患者的肾功能可能受损。已开发出用于治疗急性秋水仙碱和三环类抗抑郁药中毒的Fab片段制剂,但尚未商业化。秋水仙碱中毒在西方国家很少见,即使在严重的三环类抗抑郁药过量中毒情况下,药物治疗和支持性护理通常也有效。已尝试制备能够增强百草枯从肺部清除的抗百草枯抗体,但迄今为止所有此类尝试均已证明不成功。

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