| Literature DB >> 30856290 |
Huitong Ruan1,2,3,4, Quanyin Hu1,3,4, Di Wen1,3,4, Qian Chen1,3,4, Guojun Chen1,3,4, Yifei Lu1,3,4, Jinqiang Wang1,3,4, Hao Cheng5, Weiyue Lu2, Zhen Gu1,3,4.
Abstract
Patients with advanced melanoma that is of low tumor-associated antigen (TAA) expression often respond poorly to PD-1/PD-L1 blockade therapy. Epigenetic modulators, such as hypomethylation agents (HMAs), can enhance the antitumor immune response by inducing TAA expression. Here, a dual bioresponsive gel depot that can respond to the acidic pH and reactive oxygen species (ROS) within the tumor microenvironment (TME) for codelivery of anti-PD1 antibody (aPD1) and Zebularine (Zeb), an HMA, is engineered. aPD1 is first loaded into pH-sensitive calcium carbonate nanoparticles (CaCO3 NPs), which are then encapsulated in the ROS-responsive hydrogel together with Zeb (Zeb-aPD1-NPs-Gel). It is demonstrated that this combination therapy increases the immunogenicity of cancer cells, and also plays roles in reversing immunosuppressive TME, which contributes to inhibiting the tumor growth and prolonging the survival time of B16F10-melanoma-bearing mice.Entities:
Keywords: bioresponsive materials; drug delivery; epigenetic modulation; immune checkpoint blockade; immunotherapy
Mesh:
Substances:
Year: 2019 PMID: 30856290 DOI: 10.1002/adma.201806957
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849