Dr. Philip Leighton
Sr. Director, Molecular Biology at Ligand Pharmaceuticals Incorporated
Dr. Leighton is Senior Director of Molecular Biology at Ligand Pharmaceuticals in Emeryville, CA. He received his Ph.D in Molecular Biology from Princeton University, followed by post-doctoral studies at the University of California, San Francisco. At Ligand, he is responsible for the development and validation of the OmniChicken® portion of the OmniAb® platform for the production of human antibodies in transgenic chickens. In addition to OmniChickens expressing normal human antibodies, he has more recently developed OmniClic® chickens expressing a common light chain for bispecific antibody discovery. Currently under development are OmniDabTM chickens expressing single domain antibodies, and the OmniTaurTM platform for heavy chains with ultralong CDR-H3s. OmniChickens are currently being used in a number of programs by pharmaceutical industry partners.
Title: Heavy Chain Only Antibodies to SARS-CoV-2
Since the first monoclonal antibody therapy was approved almost forty years ago, the technologies and strategies used in the discovery and expression of immunotherapies have continued to evolve. While the first approved therapies were chimeric proteins or humanized scaffolds, today, transgenic animals dominate discovery platforms. While early therapies derived from mice, today, many different species demonstrate their unique advantages in the field. Because of its phylogenetic distance from humans, the chicken can often generate a superior immune response compared to mice when looking for antibodies to highly conserved proteins. Similarly, camelids express a single domain antibody, a so-called VHH, a heavy chain that does not require a light chain to be co-expressed. The resulting molecule is significantly smaller than an IgG and at an advantage when the targeted epitope is small or partially hidden. We have developed the OmniDAB© chicken, a chicken capable of expressing an autonomous heavy chain. These heavy chain only birds mount a robust immune response to a model antigen and display wide epitope coverage. This talk will discuss our recent work using the OmniDAB platform to generate functional, high affinity antibodies to the spike protein of SARS-CoV-2.