Engineering Au 44 Nanoclusters for NIR-II Luminescence Imaging-Guided Photoactivatable Cancer Immunotherapy.
Ge YangXinxin PanWenbi FengQiaofeng YaoFuyi JiangFanglin DuXianfeng ZhouJianping XieXun YuanPublished in: ACS nano (2023)
Immunotherapy is an advanced therapeutic strategy of cancer treatment but suffers from the issues of off-target adverse effects, lack of real-time monitoring techniques, and unsustainable response. Herein, an ultrasmall Au nanocluster (NC)-based theranostic probe is designed for second near-infrared window (NIR-II) photoluminescence (PL) imaging-guided phototherapies and photoactivatable cancer immunotherapy. The probe (Au 44 MBA 26 -NLG for short) is composed of atomically precise and NIR-II emitting Au 44 MBA 26 NCs (here MBA denotes water-soluble 4-mercaptobenzoic acid) conjugated with immune checkpoint inhibitor 1-cyclohexyl-2-(5H-imidazo[5,1- a ]isoindol-5-yl)ethanol (NLG919) via a singlet oxygen ( 1 O 2 )-cleavable linker. Upon NIR photoirradiation, the Au 44 MBA 26 -NLG not only enables NIR-II PL imaging of tumors in deep tissues for guiding tumor therapy but also allows the leverage of photothermal property for cancer photothermal therapy (PTT) and the photogenerated 1 O 2 for photodynamic therapy (PDT) and releasing NLG919 for cancer immunotherapy. Such a multiple effect modulated by Au 44 MBA 26 -NLG prompts the proliferation and activation of effector T cells, upshifts systemic antitumor T-lymphocyte (T cell) immunity, and finally suppresses the growth of both primary and distant tumors in living mice. Overall, this study may provide a promising theranostic nanoplatform toward NIR-II PL imaging-guided phototherapies and photoactivatable cancer immunotherapy.
Keyphrases
- photodynamic therapy
- fluorescence imaging
- sensitive detection
- quantum dots
- high resolution
- reduced graphene oxide
- drug release
- fluorescent probe
- energy transfer
- water soluble
- signaling pathway
- type diabetes
- lymph node
- metabolic syndrome
- gold nanoparticles
- insulin resistance
- bone marrow
- dendritic cells
- stem cells
- skeletal muscle
- cell therapy
- immune response
- high fat diet induced