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Protein A-immunoadsorption (Prosorba~R column) in the treatment of rheumatoid arthritis

机译:蛋白质A-ImmunoOcallinal(Prosorba〜R柱)治疗类风湿性关节炎

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摘要

New pathophysiological concepts are beginning to emerge for rheumatoid arthritis (RA). Studies establishing a key role for tumor necrosis factor alpha (TNFalpha) in rheumatoid synovialinflammation led to the development of anti-TNFalpha agents, which were then proved effective. However, TNFa inactivation depresses the immune system, increasing the risk of infection. This drawback, together with the recent emphasis on anti-filaggrin autoantibody production, may rekindle interest in plasma exchange as a treatment alternative in patients with RA.For many years, plasma exchange was the only technique capable of clearing the plasma of substances with possible pathogenic effects. However, plasma exchange produced partial or disappointing results in patients with RA. Plasma exchange is a nonselective method and requires the removal of several liters of plasma (60 ml/kg on average) and its replacement by an equivalent volume of plasma substitutes such as albumin. In the 1980s, immunoadsorption was suggested asan alternative to plasma exchange for removing noxious substances from the plasma of patients with autoimmune diseases refractory to conventional treatments. Candidate diseases for immunoadsorption were autoimmune conditions due to known factors that were removable by physical, chemical or immunological techniques, such as myasthe-nia, autoimmune thrombocytopenic purpura, coagulation factor inhibitor production systemic lupus erythematosus, and idiopathic dilated cardiomyopathy .Immunoadsorption is more selective than plasma exchange, as it does not remove plasma proteins such as albumin and clotting factors. In addition, immunoadsorption does not require administration of plasma substitutes and therefore does not expose patients to the potential side effects of these compounds. Albumin preparations, for instance, are obtained from human sources and may be capable of transmitting infectious agents. In 1999, the Food and Drug Administration licensed protein A-immunoadsorption on the Prosorba~R column for patients with refractory RA.
机译:新的病理生理学概念开始出现类风湿性关节炎(RA)。在类风湿滑膜炎症中建立肿瘤坏死因子α(TNFalpha)的关键作用导致抗TNFalpha剂的发育,然后证明有效。然而,TNFA失活抑制免疫系统,增加了感染的风险。这种缺点在于最近强调抗氟代林自身抗体产量,可以重新抑制血浆交换的兴趣作为RA的患者的治疗方法。多年来,血浆交换是唯一能够用可能致病的物质清除物质血浆的唯一技术效果。然而,血浆交换在RA患者中产生了部分或令人失望的结果。等离子体交换是一种非选择性方法,需要除去几种血浆(平均60ml / kg)的血浆(60ml / kg)及其替代物等同的等离子体替代品如白蛋白。在20世纪80年代,提出了asan替代血浆交换的替代,用于从自身免疫疾病令人难以忍受的常规治疗中去除来自患者的血浆的有毒物质。免疫吸附的候选疾病是由于身体,化学或免疫技术可拆卸的已知因素,例如MyAsthe-Nia,自身免疫性血小板减少紫癜,凝血因子抑制剂生产全身狼疮红斑狼疮和特发性扩张的心肌病.IMMunoadalling比等离子体交换,因为它不会去除血浆蛋白,如白蛋白和凝血因子。此外,免疫吸收不需要施用血浆替代物,因此不会将患者暴露于这些化合物的潜在副作用。例如,从人来源获得白蛋白制剂,并且可以能够传递传染性剂。 1999年,食品和药物管理局对耐火RA患者的ProSorba〜R柱上的蛋白质A-ImmunoLation。

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