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Open AccessEditor’s ChoiceReview

Immunogenicity of Innovative and Biosimilar Monoclonal Antibodies

Department of Pharmaceutical Sciences, Utrecht University, 3512 JE Utrecht, The Netherlands
Author to whom correspondence should be addressed.
Antibodies 2019, 8(1), 21;
Received: 13 February 2019 / Accepted: 27 February 2019 / Published: 5 March 2019
(This article belongs to the Special Issue Structure and Function of Antibodies)
The development of hybridoma technology for producing monoclonal antibodies (mAbs) by Kohler and Milstein (1975) counts as one of the major medical breakthroughs, opening up endless possibilities for research, diagnosis and for treatment of a whole variety of diseases. Therapeutic mAbs were introduced three decades ago. The first generation of therapeutic mAbs of murine origin showed high immunogenicity, which limited efficacy and was associated with severe infusion reactions. Subsequently chimeric, humanized, and fully human antibodies were introduced as therapeutics, these mAbs were considerably less immunogenic. Unexpectedly humanized mAbs generally show similar immunogenicity as chimeric antibodies; based on sequence homology chimeric mAbs are sometimes more “human” than humanized mAbs. With the introduction of the regulatory concept of similar biological medicines (biosimilars) a key concern is the similarity in terms of immunogenicity of these biosimilars with their originators. This review focuses briefly on the mechanisms of induction of immunogenicity by biopharmaceuticals, mAbs in particular, in relation to the target of the immune system. View Full-Text
Keywords: biopharmaceuticals; monoclonal antibodies; biosimilars; immunogencitity; B-cell tolerance; aggregates; anti-idiotypic biopharmaceuticals; monoclonal antibodies; biosimilars; immunogencitity; B-cell tolerance; aggregates; anti-idiotypic
MDPI and ACS Style

Doevendans, E.; Schellekens, H. Immunogenicity of Innovative and Biosimilar Monoclonal Antibodies. Antibodies 2019, 8, 21.

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