免疫原性
获得性免疫系统
免疫系统
免疫学
先天免疫系统
生物
免疫
医学
作者
Sivan Cohen,Shan Chung
出处
期刊:Bioanalysis
[Newlands Press Ltd]
日期:2021-06-14
卷期号:13 (13): 1071-1081
被引量:6
标识
DOI:10.4155/bio-2021-0077
摘要
Development of antidrug antibodies (ADAs) is an undesirable potential outcome of administration of biotherapeutics and involves the innate and adaptive immune systems. ADAs can have detrimental clinical consequences: they can reduce biotherapeutic efficacy or produce adverse events. Because animal models are considered poor predictors of immunogenicity in humans, in vitro assays with human innate and adaptive immune cells are commonly used alternatives that can reveal cell-mediated unwanted immune responses. Multiple methods have been developed to assess the immune cell response following exposure to biotherapeutics and estimate the potential immunogenicity of biotherapeutics. This review highlights the role of innate and adaptive immune cells as the drivers of immunogenicity and summarizes the use of these cells in assays to predict clinical ADA.
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