Publication | Closed Access
Engineering Au<sub>44</sub> Nanoclusters for NIR-II Luminescence Imaging-Guided Photoactivatable Cancer Immunotherapy
95
Citations
43
References
2023
Year
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<sub>44</sub>MBA<sub>26</sub>-NLG for short) is composed of atomically precise and NIR-II emitting Au<sub>44</sub>MBA<sub>26</sub> NCs (here MBA denotes water-soluble 4-mercaptobenzoic acid) conjugated with immune checkpoint inhibitor 1-cyclohexyl-2-(5H-imidazo[5,1-<i>a</i>]isoindol-5-yl)ethanol (NLG919) via a singlet oxygen (<sup>1</sup>O<sub>2</sub>)-cleavable linker. Upon NIR photoirradiation, the Au<sub>44</sub>MBA<sub>26</sub>-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 <sup>1</sup>O<sub>2</sub> for photodynamic therapy (PDT) and releasing NLG919 for cancer immunotherapy. Such a multiple effect modulated by Au<sub>44</sub>MBA<sub>26</sub>-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.
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