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Checkpoint blockade and nanosonosensitizer-augmented noninvasive sonodynamic therapy combination reduces tumour growth and metastases in mice

机译:检查点封锁和纳米超声增敏剂增强的无创声波动力疗法组合可减少小鼠的肿瘤生长和转移

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摘要

Combined checkpoint blockade (e.g., PD1/PD-L1) with traditional clinical therapies can be hampered by side effects and low tumour-therapeutic outcome, hindering broad clinical translation. Here we report a combined tumour-therapeutic modality based on integrating nanosonosensitizers-augmented noninvasive sonodynamic therapy (SDT) with checkpoint-blockade immunotherapy. All components of the nanosonosensitizers (HMME/R837@Lip) are clinically approved, wherein liposomes act as carriers to co-encapsulate sonosensitizers (hematoporphyrin monomethyl ether (HMME)) and immune adjuvant (imiquimod (R837)). Using multiple tumour models, we demonstrate that combining nanosonosensitizers-augmented SDT with anti-PD-L1 induces an anti-tumour response, which not only arrests primary tumour progression, but also prevents lung metastasis. Furthermore, the combined treatment strategy offers a long-term immunological memory function, which can protect against tumour rechallenge after elimination of the initial tumours. Therefore, this work represents a proof-of-concept combinatorial tumour therapeutics based on noninvasive tumours-therapeutic modality with immunotherapy.
机译:副作用和低肿瘤治疗结局可能会妨碍将检查点封锁(例如PD1 / PD-L1)与传统临床疗法结合使用,从而阻碍广泛的临床翻译。在这里,我们报告了基于纳米超声增敏剂增强的无创声波动力疗法(SDT)与检查点封锁免疫疗法相结合的肿瘤治疗方式。纳米超声增敏剂(HMME / R837 @ Lip)的所有成分均已临床批准,其中脂质体充当载体以共同包裹声敏剂(血卟啉单甲醚(HMME))和免疫佐剂(咪喹莫特(R837))。使用多个肿瘤模型,我们证明,将纳米超声增敏剂增强的SDT与抗PD-L1组合可诱导抗肿瘤反应,不仅阻止原发性肿瘤进展,而且还可以防止肺转移。此外,联合治疗策略可提供长期的免疫记忆功能,可在消除初始肿瘤后防止肿瘤再发。因此,这项工作代表了一种基于非侵入性肿瘤治疗方法和免疫疗法的概念验证性组合肿瘤疗法。

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