| Literature DB >> 31294571 |
Qian Chen1,2, Guojun Chen, Jiawen Chen1, Jingjing Shen1, Xudong Zhang, Jinqiang Wang2, Amanda Chan, Zhen Gu2.
Abstract
Despite the promising efficacy of immune checkpoint blockade (ICB) in treating many types of cancers, the clinical benefits have often been restricted by the low objective response rates and systemic immune-related adverse events. Here, a bioresponsive ICB treatment is developed based on the reactive oxygen species (ROS)-sensitive protein complex for controlled sequential release of anti- "don't eat me" signal antibody (aCD47) and antiprogrammed cell death protein 1 (aPD1), by leveraging the abundant ROS in the tumor microenvironment (TME). These protein complexes can also act as scavengers of ROS in the TME to reverse the immunosuppressive responses, thereby enhancing antitumor efficacy in vivo. In a melanoma cancer model, the synergistic antitumor efficacy was achieved, which was accompanied by enhanced T cell immune responses together with reduced immunosuppressive responses.Entities:
Keywords: Drug delivery; bioresponsive; immune checkpoint blockade; immunotherapy; nanomedicine
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Year: 2019 PMID: 31294571 DOI: 10.1021/acs.nanolett.9b00584
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189