A homogeneous SIRPα-CD47 cell-based, ligand-binding assay: Utility for small molecule drug development in immuno-oncology.
CD47 is an immune checkpoint protein that downregulates both the innate and adaptive anti-tumor immune response via its counter receptor SIRPα. Biologics, including humanized CD47 monoclonal antibodies and decoy SIRPα receptors, that block the SIRPα-CD47 interaction, are currently being developed as...
Main Authors: | Teresa L Burgess, Joshua D Amason, Jeffrey S Rubin, Damien Y Duveau, Laurence Lamy, David D Roberts, Catherine L Farrell, James Inglese, Craig J Thomas, Thomas W Miller |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2020-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0226661 |
Similar Items
-
Quantitative high-throughput screening assays for the discovery and development of SIRPα-CD47 interaction inhibitors.
by: Thomas W Miller, et al.
Published: (2019-01-01) -
Repositioning Azelnidipine as a Dual Inhibitor Targeting CD47/SIRPα and TIGIT/PVR Pathways for Cancer Immuno-Therapy
by: Xiuman Zhou, et al.
Published: (2021-05-01) -
Characterisation of the SIRP gene family and CD47 viral homologues
by: Cochrane, Fiona Gutiez
Published: (2005) -
Role of the CD47/SIRPα-interaction in regulation of macrophage phagocytosis
by: Olsson, Mattias
Published: (2008) -
CD47–SIRPα : an interaction of importance for bone cell differentiation
by: Koskinen, Cecilia
Published: (2014)