Engineered human FcγRIIa fusion: A novel strategy to extend serum half‐life of therapeutic proteins

Abstract The immunoglobulin G (IgG) molecule has a long circulating serum half‐life (~3 weeks) through pH‐ dependent FcRn binding‐mediated recycling. To hijack the intracellular trafficking and recycling mechanism of IgG as a way to extend serum persistence of non‐antibody therapeutic proteins, we have evolved the ectodomain of a low‐affinity human FcγRIIa for enhanced binding to the lower hinge and upper CH2 region of IgG, which is very far from the FcRn binding site (CH2–CH3 interface). High‐throughput library screening enabled isolation of an FcγRIIa variant (2A45.1) with 32‐fold increased binding affinity to human IgG1 Fc (equilibrium dissociation constant: 9.04 × 10−7 M for wild type FcγRIIa and 2.82 × 10−8 M for 2A45.1) and significantly improved affinity to mouse serum IgG compared to wild type human FcγRIIa. The in vivo pharmacokinetic profile of PD‐L1 fused with engineered FcγRI…