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本文引用的文献

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Eradication of spontaneous malignancy by local immunotherapy.局部免疫疗法根除自发性恶性肿瘤。
Sci Transl Med. 2018 Jan 31;10(426). doi: 10.1126/scitranslmed.aan4488.
2
Concurrent PD-1 Blockade Negates the Effects of OX40 Agonist Antibody in Combination Immunotherapy through Inducing T-cell Apoptosis.OX40 激动剂抗体联合免疫疗法中 PD-1 阻断通过诱导 T 细胞凋亡而失效。
Cancer Immunol Res. 2017 Sep;5(9):755-766. doi: 10.1158/2326-6066.CIR-17-0292.
3
Imaging B Cells in a Mouse Model of Multiple Sclerosis Using Cu-Rituximab PET.使用铜标记的利妥昔单抗PET对多发性硬化症小鼠模型中的B细胞进行成像。
J Nucl Med. 2017 Nov;58(11):1845-1851. doi: 10.2967/jnumed.117.189597. Epub 2017 Jul 7.
4
Predicting the response to CTLA-4 blockade by longitudinal noninvasive monitoring of CD8 T cells.通过对CD8 T细胞进行纵向无创监测来预测对CTLA-4阻断的反应。
J Exp Med. 2017 Aug 7;214(8):2243-2255. doi: 10.1084/jem.20161950. Epub 2017 Jun 30.
5
Development of novel avenues to overcome challenges facing CAR T cells.开发克服嵌合抗原受体T细胞所面临挑战的新途径。
Transl Res. 2017 Sep;187:22-31. doi: 10.1016/j.trsl.2017.05.009. Epub 2017 Jun 10.
6
Cellular immunotherapies for cancer.癌症的细胞免疫疗法
Oncoimmunology. 2017 May 2;6(5):e1306619. doi: 10.1080/2162402X.2017.1306619. eCollection 2017.
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A PET Imaging Strategy to Visualize Activated T Cells in Acute Graft-versus-Host Disease Elicited by Allogenic Hematopoietic Cell Transplant.一种用于可视化同种异体造血细胞移植引发的急性移植物抗宿主病中活化T细胞的正电子发射断层显像(PET)成像策略。
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9
Granzyme B PET Imaging as a Predictive Biomarker of Immunotherapy Response.颗粒酶B正电子发射断层扫描成像作为免疫治疗反应的预测生物标志物
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10
CpG oligodeoxynucleotide nanomedicines for the prophylaxis or treatment of cancers, infectious diseases, and allergies.用于预防或治疗癌症、传染病和过敏症的CpG寡脱氧核苷酸纳米药物。
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影像学激活的 T 细胞可预测癌症疫苗的反应。

Imaging activated T cells predicts response to cancer vaccines.

机构信息

Department of Radiology.

Molecular Imaging Program at Stanford.

出版信息

J Clin Invest. 2018 Jun 1;128(6):2569-2580. doi: 10.1172/JCI98509. Epub 2018 May 14.

DOI:10.1172/JCI98509
PMID:29596062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5983309/
Abstract

In situ cancer vaccines are under active clinical investigation, given their reported ability to eradicate both local and disseminated malignancies. Intratumoral vaccine administration is thought to activate a T cell-mediated immune response, which begins in the treated tumor and cascades systemically. In this study, we describe a PET tracer (64Cu-DOTA-AbOX40) that enabled noninvasive and longitudinal imaging of OX40, a cell-surface marker of T cell activation. We report the spatiotemporal dynamics of T cell activation following in situ vaccination with CpG oligodeoxynucleotide in a dual tumor-bearing mouse model. We demonstrate that OX40 imaging was able to predict tumor responses on day 9 after treatment on the basis of tumor tracer uptake on day 2, with greater accuracy than both anatomical and blood-based measurements. These studies provide key insights into global T cell activation following local CpG treatment and indicate that 64Cu-DOTA-AbOX40 is a promising candidate for monitoring clinical cancer immunotherapy strategies.

摘要

原位癌症疫苗正在进行积极的临床研究,因为它们据称能够消除局部和播散性恶性肿瘤。瘤内疫苗给药被认为可以激活 T 细胞介导的免疫反应,该反应始于治疗的肿瘤,并在系统中级联。在这项研究中,我们描述了一种 PET 示踪剂(64Cu-DOTA-AbOX40),它能够对 T 细胞激活的细胞表面标志物 OX40 进行非侵入性和纵向成像。我们报告了在双肿瘤荷瘤小鼠模型中,用 CpG 寡脱氧核苷酸进行原位疫苗接种后 T 细胞激活的时空动力学。我们证明,基于第 2 天的肿瘤示踪剂摄取,OX40 成像能够在治疗后第 9 天预测肿瘤反应,其准确性高于解剖学和基于血液的测量。这些研究为局部 CpG 治疗后全身 T 细胞激活提供了重要的见解,并表明 64Cu-DOTA-AbOX40 是监测临床癌症免疫治疗策略的有前途的候选物。