Fischer Nicolas, Elson Greg, Magistrelli Giovanni, Dheilly Elie, Fouque Nicolas, Laurendon Amélie, Gueneau Franck, Ravn Ulla, Depoisier Jean-François, Moine Valery, Raimondi Sylvain, Malinge Pauline, Di Grazia Laura, Rousseau François, Poitevin Yves, Calloud Sébastien, Cayatte Pierre-Alexis, Alcoz Mathias, Pontini Guillemette, Fagète Séverine, Broyer Lucile, Corbier Marie, Schrag Delphine, Didelot Gérard, Bosson Nicolas, Costes Nessie, Cons Laura, Buatois Vanessa, Johnson Zoe, Ferlin Walter, Masternak Krzysztof, Kosco-Vilbois Marie
Novimmune SA, 14 chemin des Aulx, CH-1228 Plan-les-Ouates, Switzerland.
Nat Commun. 2015 Feb 12;6:6113. doi: 10.1038/ncomms7113.
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.
双特异性抗体能够实现独特的治疗方法,但在工业规模上生产它们仍然是一项挑战,并且为实现双特异性而引入的修饰通常会对稳定性和免疫原性风险产生影响。在此,我们描述了一种完全人源的双特异性IgG,它没有任何修饰,可以通过一个平台工艺在工业规模上生产。这种形式被称为κλ体,通过共表达一条重链和两条不同的轻链(一条κ链和一条λ链)组装而成。使用十个不同的靶点,我们证明轻链在介导特异性和高亲和力方面可以发挥主导作用。κλ体支持多种作用模式,其稳定性和药代动力学特性与治疗性抗体无异。因此,κλ体代表了一种独特的、完全人源的形式,它利用轻链可变区进行抗原结合,利用轻链恒定区进行稳健的下游加工,以实现双特异性抗体的潜力。