Nature Communications · 2015 · 119 citations · 31 references
PharmacyBiotechnologyImmunologyAntibody EngineeringImmunotechnologyProtein EngineeringAntibody PharmacokineticsAntibody PurificationAntibody StabilityBispecific AntibodiesLigand BindingTherapeutic Antibody DevelopmentAntibodiesBispecific Antibody DiscoveryBispecific Antibody FormatsBispecific Antibody ManufacturingBispecific Antibody SelectionExpression Of Bispecific AntibodiesManufacturing Of Bispecific AntibodiesPurification
Bispecific antibodies enable unique therapeutic approaches but it remains a challenge to produce them at the industrial scale, and the modifications introduced to achieve bispecificity often have an impact on stability and risk of immunogenicity. Here we describe a fully human bispecific IgG devoid of any modification, which can be produced at the industrial scale, using a platform process. This format, referred to as a κλ-body, is assembled by co-expressing one heavy chain and two different light chains, one κ and one λ. Using ten different targets, we demonstrate that light chains can play a dominant role in mediating specificity and high affinity. The κλ-bodies support multiple modes of action, and their stability and pharmacokinetic properties are indistinguishable from therapeutic antibodies. Thus, the κλ-body represents a unique, fully human format that exploits light-chain variable domains for antigen binding and light-chain constant domains for robust downstream processing, to realize the potential of bispecific antibodies.
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Naturally occurring antibodies devoid of light chains
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Pharmacy, Biochemistry, Immunology +14
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Medicine, Immunology, Oncology +14
Tumor Regression in Cancer Patients by Very Low Doses of a T Cell–Engaging Antibody
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Life Sciences, Immunology, Oncology +17