How to predict and prevent the immunogenicity of therapeutic proteins.

Huub Schellekens
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引用次数: 94

Abstract

Therapeutic proteins in general induce an immune response, especially when administered as multiple doses over prolonged periods. Non-human therapeutic proteins such as asparaginase and streptokinase induce antibodies by the classical immune reaction and their primary immunogenic factor is the degree of non-self. Human therapeutic proteins such as the interferons and GM-CSF breakdown immune tolerance and protein aggregation is their main factor inducing antibodies. Many other factors influence the level of immunogenicity of proteins, such as storage conditions,contaminants or impurities in the preparation, downstream processing, dose and length of treatment, as well as route of administration, appropriate formulation and disease status and concomitant treatment of patients. Clinical manifestations of antibodies directed against the protein include loss of efficacy, cross neutralization of endogenous proteins and general immune system effects, such as anaphylaxis or serum sickness.

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如何预测和预防治疗性蛋白的免疫原性。
治疗性蛋白质通常会引起免疫反应,特别是在长时间多次给药的情况下。非人类治疗性蛋白如天冬酰胺酶和链激酶通过经典的免疫反应诱导抗体,其主要的免疫原性因子是非自体程度。人治疗性蛋白如干扰素和GM-CSF分解免疫耐受和蛋白聚集是其诱导抗体的主要因素。许多其他因素影响蛋白质的免疫原性水平,如储存条件、制备中的污染物或杂质、下游加工、剂量和治疗时间,以及给药途径、适当的配方和疾病状况以及患者的伴随治疗。针对该蛋白的抗体的临床表现包括药效丧失、内源性蛋白交叉中和和一般免疫系统效应,如过敏反应或血清病。
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