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近红外光免疫疗法治疗癌症后急性生理反应的体内成像

In vivo imaging of acute physiological responses after treatment of cancer with near-infrared photoimmunotherapy.

作者信息

Nakajima Kohei, Sugikawa Akiyo, Yasui Hironobu, Higashikawa Kei, Suzuki Chie, Natsume Takahiro, Suzuki Motofumi, Takakura Hideo, Tomita Mayu, Takahashi Sachi, Hirata Kenji, Magata Yasuhiro, Kuge Yuji, Ogawa Mikako

机构信息

Laboratory of Bioanalysis and Molecular Imaging, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Hokkaido, 060-0812, Japan.

Global Station for Biosurfaces and Drug Discovery, Global Institution for Collaborative Research and Education (GI-CoRE), Hokkaido University, Sapporo, Hokkaido, Japan.

出版信息

Mol Imaging Biol. 2023 Aug;25(4):648-658. doi: 10.1007/s11307-023-01822-9. Epub 2023 May 16.

Abstract

PURPOSE

Near-infrared photoimmunotherapy (NIR-PIT) is a new cancer phototherapy using an antibody-photosensitizer conjugate (Ab-IR700). By NIR light irradiation, Ab-IR700 forms a water-insoluble aggregation on the plasma membrane of cancer cells, leading to lethal membrane damage of cancer cells with high selectivity. However, IR700 produces singlet oxygen, which induces non-selective inflammatory responses such as edema in normal tissues around the tumor. Understanding such treatment-emergent responses is important to minimize side effects and improve clinical outcomes. Thus, in this study, we evaluated physiological responses during NIR-PIT by magnetic resonance imaging (MRI) and positron emission tomography (PET).

PROCEDURES

Ab-IR700 was intravenously injected into tumor-bearing mice with two tumors on the right and left sides of the dorsum. At 24 h after injection, a tumor was irradiated with NIR light. Edema formation was examined by T1/T2/diffusion-weighted MRI and inflammation was investigated by PET with 2-deoxy-2-[F]fluoro-D-glucose ([F]FDG). Because inflammation can increase vascular permeability via inflammatory mediators, we evaluated changes in oxygen levels in tumors using a hypoxia imaging probe, [F]fluoromisonidazole ([F]FMISO).

RESULTS

The uptake of [F]FDG in the irradiated tumor was significantly decreased compared to the control tumor, indicating the impairment of glucose metabolism induced by NIR-PIT. MRI and [F]FDG-PET images showed that inflammatory edema with [F]FDG accumulation was present in the surrounding normal tissues of the irradiated tumor. Furthermore, [F]FMISO accumulation in the center of the irradiated tumor was relatively low, indicating the enhancement of oxygen supply due to increased vascular permeability. In contrast, high [F]FMISO accumulation was observed in the peripheral region, indicating enhancement of hypoxia in the region. This could be because inflammatory edema was formed in the surrounding normal tissues, which blocked blood flow to the tumor.

CONCLUSIONS

We successfully monitored inflammatory edema and changes in oxygen levels during NIR-PIT. Our findings on the acute physiological responses after light irradiation will help to develop effective measures to minimize the side effects in NIR-PIT.

摘要

目的

近红外光免疫疗法(NIR-PIT)是一种使用抗体-光敏剂偶联物(Ab-IR700)的新型癌症光疗法。通过近红外光照射,Ab-IR700在癌细胞的质膜上形成水不溶性聚集体,导致癌细胞的致命膜损伤,具有高度选择性。然而,IR700会产生单线态氧,诱导非选择性炎症反应,如肿瘤周围正常组织的水肿。了解这种治疗引发的反应对于最小化副作用和改善临床结果很重要。因此,在本研究中,我们通过磁共振成像(MRI)和正电子发射断层扫描(PET)评估了NIR-PIT期间的生理反应。

程序

将Ab-IR700静脉注射到背部左右两侧有两个肿瘤的荷瘤小鼠体内。注射后24小时,用近红外光照射一个肿瘤。通过T1/T2/扩散加权MRI检查水肿形成情况,并通过2-脱氧-2-[F]氟-D-葡萄糖([F]FDG)PET研究炎症情况。由于炎症可通过炎症介质增加血管通透性,我们使用缺氧成像探针[F]氟米索硝唑([F]FMISO)评估肿瘤中的氧水平变化。

结果

与对照肿瘤相比,照射肿瘤中[F]FDG的摄取显著降低,表明NIR-PIT诱导了葡萄糖代谢受损。MRI和[F]FDG-PET图像显示,照射肿瘤周围的正常组织中存在伴有[F]FDG积聚的炎性水肿。此外,照射肿瘤中心的[F]FMISO积聚相对较低,表明由于血管通透性增加导致氧供应增强。相反,在周边区域观察到高[F]FMISO积聚,表明该区域缺氧增强。这可能是因为周围正常组织中形成了炎性水肿,阻断了流向肿瘤的血流。

结论

我们成功监测了NIR-PIT期间的炎性水肿和氧水平变化。我们关于光照射后急性生理反应的研究结果将有助于制定有效措施,以最小化NIR-PIT中的副作用。

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