体积纳米微滴增强超声手术联合免疫检查点抑制作为癌症治疗平台

IF 12.1 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2025-03-10 DOI:10.1002/smll.202411474
Bar Glickstein, Mike Bismuth, Roni Gattegno, Tiran Bercovici, Oz Shaul, Ramona Aronovich, Galit Horn, Anat Globerson Levin, Yi Feng, Tali Ilovitsh
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引用次数: 0

摘要

免疫检查点抑制剂很有前景,但其在实体肿瘤中的疗效受到复杂的肿瘤微环境和缺乏免疫细胞浸润的限制。本研究旨在通过结合抗PD-1检查点抑制疗法和纳米微滴介导的组织切片法来增强免疫治疗。提出的方法包括全身注射纳米液滴,这些纳米液滴会在肿瘤内积聚。然后使用旋转成像探针将这些纳米液滴激活为空化气泡,然后使用低频超声应用。这一过程诱导肿瘤分化,促进肿瘤微环境由冷向热的转变。肿瘤消融结果显示癌组织内有广泛病变,证明了消融治疗的有效性。与对照组相比,纳米液滴、超声和抗PD-1联合使用的方法显著降低了肿瘤的生长。免疫组化分析显示,肿瘤治疗组F4/80+巨噬细胞和CD8+ T细胞增加,表明免疫应答增强。F4/80+巨噬细胞募集率为21.36%±3.4%,CD8+ t细胞募集率为6.76%±4.5%,分别是对照组的6.8倍和5.5倍。这种方法通过结合精确的机械破坏和全身免疫激活,证明了克服实体瘤治疗关键障碍的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Volumetric Nanodroplet-Enhanced Ultrasound Surgery Combined with Immune Checkpoint Inhibition as a Cancer Therapy Platform

Volumetric Nanodroplet-Enhanced Ultrasound Surgery Combined with Immune Checkpoint Inhibition as a Cancer Therapy Platform

Volumetric Nanodroplet-Enhanced Ultrasound Surgery Combined with Immune Checkpoint Inhibition as a Cancer Therapy Platform

Immune checkpoint inhibitors hold promise, yet their efficacy in solid tumors is limited by the complex tumor microenvironment and the lack of immune cell infiltration. This study aims to enhance immunotherapy by combining anti PD-1 checkpoint inhibition therapy with nanodroplet-mediated histotripsy. The proposed method involves systemic injection of nanodroplets, which accumulate within tumors. These nanodroplets are then activated into cavitating gas bubbles using a rotating imaging probe, followed by low-frequency ultrasound application. This process induces tumor fractionation, facilitating the shift of the tumor microenvironment from cold to hot. Tumor ablation results show extensive lesions within the cancerous tissues, demonstrating the effectiveness of the ablation treatment. The combined approach of nanodroplets, ultrasound and anti PD-1 yielded a significant reduction in tumor growth compared to control groups. Immunohistochemistry analysis reveals an increase in F4/80+ macrophages and CD8+ T cells in the treated tumor group, indicating an enhanced immune response. F4/80+ macrophages reached 21.36% ± 3.4%, while CD8+ T-cell recruitment achieved 6.76% ± 4.5%, representing a 6.8- and a 5.5-fold increase compared to the control group, respectively. This approach demonstrates the potential to overcome key barriers in solid tumor treatment by combining precise mechanical disruption with systemic immune activation.

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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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