Selection of a Full Agonist Combinatorial Antibody that Rescues Leptin Deficiency In Vivo

• Main Authors: Pingdong Tao, Yuanyuan Kuang, Yu Li, Wenping Li, Zibei Gao, Lili Liu, Min Qiang, Zhao Zha, Kun Fan, Peixiang Ma, Jeffrey M. Friedman, Guang Yang, Richard A. Lerner
• Format: Article
• Language: English
• Published: Wiley 2020-08-01
• Series: Advanced Science
• Subjects: combinatorial antibody library; full agonists; function‐guided selection; leptin receptors; replacement therapy
• Online Access: https://doi.org/10.1002/advs.202000818

Abstract Growth factor deficiency in adulthood constitutes a distinct clinical syndrome with significant morbidities including abnormal body composition, reduced energy, affective disturbances, dyslipidemia, and increased cardiovascular risk. Protein replacement therapies using recombinant proteins or enzymes represent the only approved treatment. Combinatorial antibodies have shown great promise as a new class of therapeutic molecules because they act as “mechanism‐based antibodies” with both agonist and antagonist activities. Using leptin, a key hormone in energy metabolism, as an example, a function‐guided approach is developed to select combinatorial antibodies with high potency and full agonist activity that substitute natural growth factors in vivo. The identified antibody shows identical biochemical properties and cellular profiles as leptin, and rescues leptin‐deficiency in ob/ob mice. Remarkably, the antibody activates leptin receptors that are otherwise nonfunctional because of mutations (L372A and A409E). Combinatorial antibodies have significant advantages over recombinant proteins for chronical usage in terms of immunological tolerance and biological stability.