作者
Nicolas Fischer,Greg Elson,Giovanni Magistrelli,Elie Dheilly,Nicolas Fouque,Amélie Laurendon,Franck Gueneau,Ulla Ravn,Jean-François Depoisier,Valéry Moine,Sylvain Raimondi,Pauline Malinge,Laura Di Grazia,François Rousseau,Yves Poitevin,Sébastien Calloud,Pierre-Alexis Cayatte,Mathias Alcoz,Guillemette Pontini,Séverine Fagète,Lucile Broyer,Marie Corbier,Delphine Schrag,Gérard Didelot,Nicolas Bosson,Nicolas Costes,Laura Cons,Vanessa Buatois,Zoë Johnson,Walter Ferlin,Krzysztof Masternak,Marie Kosco‐Vilbois
摘要
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.