Bispecific antibody generated with sortase and click chemistry has broad antiinfluenza virus activity

作者：Wagner Koen; Kwakkenbos Mark J; Claassen Yvonne B; Maijoor Kelly; Bohne Martino; van der Sluijs Koenraad F; Witte Martin D; van Zoelen Diana J; Cornelissen Lisette A; Beaumont Tim; Bakker Arjen Q; Ploegh Hidde L; Spits Hergen^*

来源：Proceedings of the National Academy of Sciences, 2014, 111(47): 16820-16825.

DOI：10.1073/pnas.1408605111

• antibody engineering
• immunotherapy
• influenza

Bispecific antibodies have therapeutic potential by expanding the functions of conventional antibodies. Many different formats of bispecific antibodies have meanwhile been developed. Most are genetic modifications of the antibody backbone to facilitate incorporation of two different variable domains into a single molecule. Here, we present a bispecific format where we have fused two full-sized IgG antibodies via their C termini using sortase transpeptidation and click chemistry to create a covalently linked IgG antibody heterodimer. By linking two potent anti-influenza A antibodies together, we have generated a full antibody dimer with bispecific activity that retains the activity and stability of the two fusion partners.

• 出版日期2014-11-25