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本文引用的文献

1
Interstitial near-infrared photoimmunotherapy: effective treatment areas and light doses needed for use with fiber optic diffusers.间质近红外光免疫疗法:使用光纤扩散器所需的有效治疗区域和光剂量。
Oncotarget. 2018 Jan 27;9(13):11159-11169. doi: 10.18632/oncotarget.24329. eCollection 2018 Feb 16.
2
Evaluation of Early Therapeutic Effects after Near-Infrared Photoimmunotherapy (NIR-PIT) Using Luciferase-Luciferin Photon-Counting and Fluorescence Imaging.近红外光免疫治疗(NIR-PIT)后应用荧光素酶-荧光素光子计数和荧光成像技术评估早期治疗效果。
Mol Pharm. 2017 Dec 4;14(12):4628-4635. doi: 10.1021/acs.molpharmaceut.7b00731. Epub 2017 Nov 22.
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Flexible laser endoscope for minimally invasive photodynamic diagnosis (PDD) and therapy (PDT) toward efficient tumor removal.用于微创光动力诊断(PDD)和治疗(PDT)以高效切除肿瘤的柔性激光内窥镜。
Opt Express. 2017 Jul 10;25(14):16795-16812. doi: 10.1364/OE.25.016795.
4
Immunogenic cancer cell death selectively induced by near infrared photoimmunotherapy initiates host tumor immunity.近红外光免疫疗法选择性诱导的免疫原性癌细胞死亡引发宿主肿瘤免疫。
Oncotarget. 2017 Feb 7;8(6):10425-10436. doi: 10.18632/oncotarget.14425.
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Flexible coaxial laser endoscope with arbitrarily selected spots in endoscopic view for photodynamic tumor therapy.用于光动力肿瘤治疗的柔性同轴激光内窥镜,在内窥镜视野中具有任意选择的光斑。
Appl Opt. 2016 Oct 20;55(30):8433-8440. doi: 10.1364/AO.55.008433.
6
Near infrared photoimmunotherapy with avelumab, an anti-programmed death-ligand 1 (PD-L1) antibody.使用抗程序性死亡配体1(PD-L1)抗体阿维鲁单抗进行近红外光免疫治疗。
Oncotarget. 2017 Jan 31;8(5):8807-8817. doi: 10.18632/oncotarget.12410.
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Near infrared photoimmunotherapy with an anti-mesothelin antibody.使用抗间皮素抗体的近红外光免疫疗法。
Oncotarget. 2016 Apr 26;7(17):23361-9. doi: 10.18632/oncotarget.8025.
8
MR imaging biomarkers for evaluating therapeutic effects shortly after near infrared photoimmunotherapy.用于评估近红外光免疫治疗后不久治疗效果的磁共振成像生物标志物。
Oncotarget. 2016 Mar 29;7(13):17254-64. doi: 10.18632/oncotarget.7357.
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Patient-derived orthotopic xenografts: better mimic of metastasis than subcutaneous xenografts.患者来源的原位异种移植:比皮下异种移植更能模拟转移。
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Combinatorial strategies for the induction of immunogenic cell death.诱导免疫原性细胞死亡的组合策略。
Front Immunol. 2015 Apr 24;6:187. doi: 10.3389/fimmu.2015.00187. eCollection 2015.

近红外光免疫治疗联合应用外部和间质光源照射。

Near Infrared Photoimmunotherapy with Combined Exposure of External and Interstitial Light Sources.

机构信息

Molecular Imaging Program, Center for Cancer Research, National Cancer Institute , National Institutes of Health , Bethesda , Maryland 20892 , United States.

出版信息

Mol Pharm. 2018 Sep 4;15(9):3634-3641. doi: 10.1021/acs.molpharmaceut.8b00002. Epub 2018 Feb 21.

DOI:10.1021/acs.molpharmaceut.8b00002
PMID:29450993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7400989/
Abstract

Near infrared photoimmunotherapy (NIR-PIT) is a new target-cell-specific cancer treatment that induces highly selective necrotic/immunogenic cell death after systemic administration of a photoabsorber antibody conjugate and subsequent NIR light exposure. However, the depth of NIR light penetration in tissue (approximately 2 cm) with external light sources limits the therapeutic effects of NIR-PIT. Interstitial light exposure using cylindrical diffusing optical fibers can overcome this limitation. The purpose in this study was to compare three NIR light delivery methods for treating tumors with NIR-PIT using a NIR laser system at an identical light energy; external exposure alone, interstitial exposure alone, and the combination. Panitumumab conjugated with the photoabsorber IRDye-700DX (pan-IR700) was intravenously administered to mice with A431-luc xenografts which are epithelial growth factor receptor (EGFR) positive. One and 2 days later, NIR light was administered to the tumors using one of three methods. Interstitial exposure alone and in combination with external sources showed the greatest decrease in bioluminescence signal intensity. Additionally, the combination of external and interstitial NIR light exposure showed significantly greater tumor size reduction and prolonged survival after NIR-PIT compared to external exposure alone. This result suggested that the combination of external and interstitial NIR light exposure was more effective than externally applied light alone. Although external exposure is the least invasive means of delivering light, the combination of external and interstitial exposures produces superior therapeutic efficacy in tumors greater than 2 cm in depth from the tissue surface.

摘要

近红外光免疫治疗(NIR-PIT)是一种新的靶向细胞特异性癌症治疗方法,它在全身给予光吸收抗体缀合物并随后进行近红外光照射后,诱导高度选择性的坏死/免疫原性细胞死亡。然而,外部光源在组织中的近红外光穿透深度(约 2 厘米)限制了 NIR-PIT 的治疗效果。使用圆柱形漫射光纤进行间质光暴露可以克服这一限制。本研究的目的是使用近红外激光系统在相同的光能量下,比较三种 NIR 光传递方法治疗 NIR-PIT 肿瘤:单独外部暴露、单独间质暴露和联合治疗。将与光吸收剂 IRDye-700DX 偶联的 panitumumab(pan-IR700)静脉注射到 A431-luc 异种移植瘤的 EGFR 阳性小鼠中。1 天和 2 天后,使用三种方法中的一种对肿瘤进行近红外光照射。单独和联合使用间质暴露显示出最大的生物发光信号强度降低。此外,与单独外部照射相比,外部和间质近红外光联合照射显示出显著更大的肿瘤体积减小和 NIR-PIT 后生存延长。这一结果表明,外部和间质近红外光联合照射比单独外部照射更有效。虽然外部照射是输送光的最微创手段,但在距组织表面大于 2 厘米深度的肿瘤中,外部和间质照射的联合应用可产生更好的治疗效果。