Clinical Manifestations of an Anti-Drug Antibody Response: Autoimmune Reactions

被引:0
|
作者
Swanson, Steven J. [1 ]
机构
[1] Amgen Inc, Dept Clin Immunol, Thousand Oaks, CA 91320 USA
来源
关键词
THERAPEUTIC PROTEINS; ERYTHROPOIETIN; IMMUNOGENICITY; DISEASE; ENZYME;
D O I
10.1089/jir.2013.0027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antibodies can be generated against a therapeutic protein upon administration to human subjects. When the therapeutic protein closely mimics one of the subject's endogenous proteins, those antibodies might bind to the endogenous protein in addition to the therapeutic protein. This scenario results when tolerance to the endogenous protein is broken. The consequences of breaking tolerance include an autoimmune response where antibodies are generated against the endogenous protein. These autoantibodies could have significant clinical relevance depending on several factors, including the redundancy of action of the endogenous protein as well as the concentration, binding affinity, and neutralizing potential of the antibodies. The consequences of a therapeutic-protein-induced autoimmune reaction can be challenging to manage as the stimulus for further perpetuation of the immune response can shift from the therapeutic protein to the endogenous protein. The potential for inducing an autoimmune response is one of the reasons that the immune response to a therapeutic protein should be monitored if it persists through the end of the study.
引用
收藏
页码:953 / 957
页数:5
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