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Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG

Author

Listed:
  • Nicolas Fischer

    (Novimmune SA)

  • Greg Elson

    (Novimmune SA
    Present address: Glenmark Pharmaceuticals SA, 5 chemin de la Combeta, CH-2300 La Chaux de Fonds, Switzerland)

  • Giovanni Magistrelli

    (Novimmune SA)

  • Elie Dheilly

    (Novimmune SA)

  • Nicolas Fouque

    (Novimmune SA)

  • Amélie Laurendon

    (Novimmune SA
    Present address: Glenmark Pharmaceuticals SA, 5 chemin de la Combeta, CH-2300 La Chaux de Fonds, Switzerland)

  • Franck Gueneau

    (Novimmune SA)

  • Ulla Ravn

    (Novimmune SA)

  • Jean-François Depoisier

    (Novimmune SA)

  • Valery Moine

    (Novimmune SA)

  • Sylvain Raimondi

    (Novimmune SA)

  • Pauline Malinge

    (Novimmune SA)

  • Laura Di Grazia

    (Novimmune SA)

  • François Rousseau

    (Novimmune SA)

  • Yves Poitevin

    (Novimmune SA)

  • Sébastien Calloud

    (Novimmune SA)

  • Pierre-Alexis Cayatte

    (Novimmune SA)

  • Mathias Alcoz

    (Novimmune SA)

  • Guillemette Pontini

    (Novimmune SA)

  • Séverine Fagète

    (Novimmune SA
    Present address: Department of Pathology and Immunology, University of Geneva, Rue Michel-Servet 1, CH-1211 Geneva 4, Switzerland)

  • Lucile Broyer

    (Novimmune SA)

  • Marie Corbier

    (Novimmune SA)

  • Delphine Schrag

    (Novimmune SA)

  • Gérard Didelot

    (Novimmune SA)

  • Nicolas Bosson

    (Novimmune SA)

  • Nessie Costes

    (Novimmune SA)

  • Laura Cons

    (Novimmune SA)

  • Vanessa Buatois

    (Novimmune SA)

  • Zoe Johnson

    (Novimmune SA)

  • Walter Ferlin

    (Novimmune SA)

  • Krzysztof Masternak

    (Novimmune SA)

  • Marie Kosco-Vilbois

    (Novimmune SA)

Abstract

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.

Suggested Citation

  • Nicolas Fischer & Greg Elson & Giovanni Magistrelli & Elie Dheilly & Nicolas Fouque & Amélie Laurendon & Franck Gueneau & Ulla Ravn & Jean-François Depoisier & Valery Moine & Sylvain Raimondi & Paulin, 2015. "Exploiting light chains for the scalable generation and platform purification of native human bispecific IgG," Nature Communications, Nature, vol. 6(1), pages 1-12, May.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7113
    DOI: 10.1038/ncomms7113
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