Ontology highlight
ABSTRACT: Purpose
While patients responding to checkpoint blockade often achieve remarkable clinical responses, there is still significant unmet need due to resistant or refractory tumors. A combination of checkpoint blockade with further T-cell stimulation mediated by 4-1BB agonism may increase response rates and durability of response. A bispecific molecule that blocks the programmed cell death 1 (PD-1)/programmed cell death 1 ligand 1 (PD-L1) axis and localizes 4-1BB costimulation to a PD-L1-positive (PD-L1+) tumor microenvironment (TME) or tumor draining lymph nodes could maximize antitumor immunity and increase the therapeutic window beyond what has been reported for anti-4-1BB mAbs.Experimental design
We generated and characterized the PD-L1/4-1BB bispecific molecule PRS-344/S0
SUBMITTER: Peper-Gabriel JK
PROVIDER: S-EPMC9662934 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature