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Abstract
Recombinant human (rhu) protein therapeutics are powerful tools to treat several severe
diseases such as multiple sclerosis and diabetes mellitus, among others. A major drawback
of these proteins is the production of anti-drug antibodies (ADAs). In some cases,
these ADAs have neutralizing capacity and can interfere with the efficacy and safety
of the drug. Little is known about the immunological mechanisms underlying the unwanted
immune response against human homolog protein therapeutics. This article aims to provide
current insights into recent immunological developments and to link this with regard
to production of ADAs. A particular focus is given to aggregates being present in
a rhu protein formulation and their impact on the immune system, subsequently leading
to breakage of tolerance and formation of ADAs. Aggregation is one of the key factors
in immunogenicity and by reducing aggregation one can reduce immunogenicity and make
drugs safer and more efficient.
Copyright 2009 Elsevier Ltd. All rights reserved.