Antibody-dependent cellular cytotoxicity-null effector developed using mammalian and plant GlycoDelete platform

Abstract

Cancer therapy using immune checkpoint inhibitor antibodies has markedly shifted the paradigm of cancer treatment. However, methods completely eliminating the effector function of these signal-regulating antibodies is urgently required. The heterogeneity of glycan chains in antibodies limits their use as therapeutic agents due to their variability; thus, the development of uniform glycan chains is necessary. Here, we subjected the anti-programmed cell death protein (PD)-1 antibody nivolumab, a representative immune checkpoint inhibitor, to GlycoDelete (GD) engineering to remove the antibody-dependent cellular cytotoxicity (ADCC) of the antibody, leaving only one glycan in the Fc. Glyco-engineered CHO cells were prepared by overexpressing endo-β-N-acetyl-glucosaminidase (Endo T) in CHO cells, in which N-acetyl-glucosaminyl-transferase I was knocked out using Cas9. GD IgG1 nivolumab and GD IgG4 nivolumab were produced using GD CHO cells, and glycan removal was confirmed using mass spectrometry. Target binding and PD-1 inhibition was not altered; however, ADCC decreased. Furthermore, the IgG4 form, determined to be the most suitable form of GD nivolumab, was produced in a plant GD system. The plant GD nivolumab also reduced ADCC without affecting PD-1 inhibitory function. Thus, CHO and plant GD platforms can be used to improve signal-regulating antibodies by reducing their effector function.

In vivo deglycosylation of recombinant glycoproteins in tobacco BY‐2 cells

“…Expression of activation associated secretory protein 1 (ASP1) from helminth in the seeds of the GlycoDelete plant showed that the two ASP1 N ‐sites were completely trimmed to a single GlcNAc (Piron et al ., 2015 ). The GlycoDelete technology was also validated in the yeast Pichia pastoris (Wang et al ., 2020 ), the filamentous fungus Aspergillus oryzae (Li et al ., 2020 ) and CHO cells (Kang et al ., 2022 ).…”