Engineering Au 44 Nanoclusters for NIR-II Luminescence Imaging-Guided Photoactivatable Cancer Immunotherapy

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...

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Veröffentlicht in:ACS nano 2023-08, Vol.17 (16), p.15605-15614
Hauptverfasser: Yang, Ge, Pan, Xinxin, Feng, Wenbi, Yao, Qiaofeng, Jiang, Fuyi, Du, Fanglin, Zhou, Xianfeng, Xie, Jianping, Yuan, Xun
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Sprache:eng
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Zusammenfassung: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 MBA -NLG for short) is composed of atomically precise and NIR-II emitting Au MBA NCs (here MBA denotes water-soluble 4-mercaptobenzoic acid) conjugated with immune checkpoint inhibitor 1-cyclohexyl-2-(5H-imidazo[5,1- ]isoindol-5-yl)ethanol (NLG919) via a singlet oxygen ( O )-cleavable linker. Upon NIR photoirradiation, the Au MBA -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 O for photodynamic therapy (PDT) and releasing NLG919 for cancer immunotherapy. Such a multiple effect modulated by Au MBA -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.
ISSN:1936-0851
1936-086X
DOI:10.1021/acsnano.3c02370