Title: CSL311, a novel, potent, therapeutic monoclonal antibody for the treatment of diseases mediated by the common beta chain of the IL-3, GM-CSF and IL-5 receptors
Authors: Panousis, C
Dhagat, U
Edwards, KM
Rayzman, V
Hardy, MP
Braley, H
Gauvreau, GM
Hercus, TR
Smith, S
Sehmi, R
McMillan, L
Dottore, M
McClure, BJ
Fabri, LJ
Vairo, G
Lopez, AF
Parker, MW
Nash, AD
Wilson, NJ
Wilson, MJ
Owczarek, CM
Issue Year: 2016
Publisher TAYLOR & FRANCIS INC
Series mAbs:
Abstract The beta common-signaling cytokines interleukin (IL)-3, granulocyte-macrophage colony stimulating factor (GM-CSF) and IL-5 stimulate pro-inflammatory activities of haematopoietic cells via a receptor complex incorporating cytokine-specific alpha and shared beta common (beta(c), CD131) receptor. Evidence from animal models and recent clinical trials demonstrate that these cytokines are critical mediators of the pathogenesis of inflammatory airway disease such as asthma. However, no therapeutic agents, other than steroids, that specifically and effectively target inflammation mediated by all 3 of these cytokines exist. We employed phage display technology to identify and optimize a novel, human monoclonal antibody (CSL311) that binds to a unique epitope that is specific to the cytokine-binding site of the human beta(c) receptor. The binding epitope of CSL311 on the beta(c) receptor was defined by X-ray crystallography and site-directed mutagenesis. CSL311 has picomolar binding affinity for the human beta(c) receptor, and at therapeutic concentrations is a highly potent antagonist of the combined activities of IL-3, GM-CSF and IL-5 on primary eosinophil survival in vitro. Importantly, CSL311 inhibited the survival of inflammatory cells present in induced sputum from human allergic asthmatic subjects undergoing allergen bronchoprovocation. Due to its high potency and ability to simultaneously suppress the activity of all 3 beta common cytokines, CSL311 may provide a new strategy for the treatment of chronic inflammatory diseases where the human beta(c) receptor is central to pathogenesis. The coordinates for the beta(c)/CSL311 Fab complex structure have been deposited with the RCSB Protein Data Bank (PDB 5DWU).
URI: https://publications.svi.edu.au/publications/6694
ISSN
Other Identifiers 10.1080/19420862.2015.1119352
Publication type Article