High Avidity IgM-Based CD20xCD3 Bispecific Antibody (IGM-2323) for Enhanced T-Cell Dependent Killing with Minimal Cytokine Release

Abstract

Unlike IgG antibodies, IgM antibodies are typically composed of a pentameric disc-like structure with 10 low affinity binding sites per molecule complexed with a joining chain (J-chain) protein. We have developed a novel T cell engaging bispecific antibody platform that utilizes the high avidity of IgM antibodies, but further combines this with the high affinity and specificity of IgG antibodies. By grafting the affinity matured binding domains of IgG antibodies onto the multimeric framework of an IgM antibody and fusing a CD3 binding single chain Fv domain to the J-chain, the resultant engineered IgM T cell bispecific antibody demonstrates strong binding to specific targets while limiting over-stimulation of engaged T cells. One of our bispecific IgM antibodies, IGM-2323, binds CD20 antigen with more than 1000 fold increased avidity and mediates complement dependent cytotoxicity (CDC) of CD20-expressing cells with greater than 100 fold higher potency when compared to the corresponding IgG bispecific. IGM-2323 also shows highly potent T cell dependent cytotoxicity, even on cells with very low cell surface expression of CD20 and on rituximab-resistant variants of Ramos cells. Significantly, IGM-2323 exhibits vastly reduced cytokine release in vitro and in vivo, with at least equivalent T cell dependent killing of CD20-expressing target cells, providing a potentially safer and more effective bispecific format than IgG-based T cell bispecifics. These data indicate that IgM-based bispecifics can induce T cell engagement and very potent cytotoxicity that can be dissociated from the cytokine release unlike what has been observed with other bispecific antibodies. In vivo efficacy studies in humanized NSG mice indicated that doses as low as 3 µg/mouse cause complete B cell elimination. Similarly, bispecific IgM completely depletes circulating B cells in cynomolgus monkeys at doses of 300 mg per kg. Furthermore, in these primate studies, durable depletion of B cells in spleen and lymphoid tissues was noted without any observable adverse effects despite repeated doses at the highest dose tested, 25 mg/kg. In these safety studies, transiently increased circulating IL-6 was measured after infusion (peak concentration less than 200 pg per mL at 4 to 8 hours post dose). The levels of TNF-alpha and IFN-gamma were only minimally increased during these primate studies. These preclinical data demonstrate the potential for broad application of this novel modular IgM-based bispecific antibody format. A Phase I dose-escalation study of IGM-2323 is currently on-going in patients with relapsed/refractory Non-Hodgkin's Lymphoma. Disclosures Baliga: IGM Biosciences: Employment, Equity Ownership. Li:IGM Biosciences: Employment, Equity Ownership. Manlusoc:IGM Biosciences: Employment, Equity Ownership. Hinton:IGM Biosciences: Employment, Equity Ownership. Ng:IGM Biosciences: Employment, Equity Ownership. Tran:IGM Biosciences: Employment, Equity Ownership. Shan:IGM Biosciences: Equity Ownership. Lu:IGM Biosciences: Employment, Equity Ownership. Saini:IGM Biosciences: Employment, Equity Ownership. Rahman:IGM Biosciences: Employment, Equity Ownership. Cao:IGM Biosciences: Employment, Equity Ownership. Saraiya:IGM Biosciences: Employment, Equity Ownership. Peterson:IGM Biosciences: Employment, Equity Ownership. Carroll:IGM Biosciences: Employment, Equity Ownership. Chen:IGM Biosciences: Employment, Equity Ownership. Keyt:IGM Biosciences: Employment, Equity Ownership.