Ontology highlight
ABSTRACT: Introduction
Despite significant clinical advancement with the use of immune checkpoint blockade (ICB) in non-small cell lung cancer (NSCLC) there are still a major subset of patients that develop adaptive/acquired resistance. Understanding resistance mechanisms to ICB is critical to developing new therapeutic strategies and improving patient survival. The dynamic nature of the tumor microenvironment and the mutational load driving tumor immunogenicity limit the efficacy to ICB. Recent studies indicate that myeloid cells are drivers of ICB resistance. In this study we sought to understand which immune cells were contributing to resistance and if we could modify them in a way to improve response to ICB therapy.Results
Our results show that combination anti-PD-1/CTLA-4 produc
SUBMITTER: Rodriguez BL
PROVIDER: S-EPMC10336223 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature