| Literature DB >> 35403784 |
Juanjuan Li1,2, Qing Xia3, Haiyan Guo1, Zhenzhen Fu1, Yong Liu4, Sisi Lin1, Jinyao Liu1.
Abstract
An approach of decorating bacteria with triple immune nanoactivators is reported to develop tumor-resident living immunotherapeutics. Under cytocompatible conditions, tumor-specific antigens and checkpoint blocking antibodies are simultaneously conjugated onto bacterial surface and then polydopamine nanoparticles are formed via in situ dopamine polymerization. In addition to serving as a linker, polydopamine with its photothermal effect can repolarize tumor-associated macrophages to a pro-inflammatory phenotype. The linked antigens promote the maturation of dendritic cells and generate tumor-specific immune responses, while the anchored antibodies block immune checkpoints and activate cytotoxic T lymphocytes. Decorated bacteria show spatiotemporal tumor retention and proliferation-dependent drug release, achieving potent antitumor effects in two antigen-overexpressing tumor models. This work provides a versatile platform to prepare multimodal and long-acting therapeutics for cancer immunotherapy.Entities:
Keywords: Antitumor Agents; Bacteria; Immunotherapy; Nanoactivators; Tumor Microenvironment
Mesh:
Year: 2022 PMID: 35403784 DOI: 10.1002/anie.202202409
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336