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在乳腺癌(MMTV-Ras)转基因小鼠模型中,MNP 和 (111)In 标记的树突状细胞的淋巴结迁移的体内成像。

In vivo imaging of lymph node migration of MNP- and (111)In-labeled dendritic cells in a transgenic mouse model of breast cancer (MMTV-Ras).

机构信息

Department of Biomedical Sciences and Technologies, Section of Radiological Sciences, University of Milan, via di Rudinì 8, 20142 Milan, Italy.

出版信息

Mol Imaging Biol. 2012 Apr;14(2):183-96. doi: 10.1007/s11307-011-0496-0.

DOI:10.1007/s11307-011-0496-0
PMID:21598093
Abstract

PURPOSE

The authors present a protocol for the in vivo evaluation, using different imaging techniques, of lymph node (LN) homing of tumor-specific dendritic cells (DCs) in a murine breast cancer model.

PROCEDURES

Bone marrow DCs were labeled with paramagnetic nanoparticles (MNPs) or (111)In-oxine. Antigen loading was performed using tumor lysate. Mature DCs were injected into the footpads of transgenic tumor-bearing mice (MMTV-Ras) and DC migration was tracked by magnetic resonance imaging (MRI) and single-photon emission computed tomography (SPECT). Ex vivo analyses were performed to validate the imaging data.

RESULTS

DC labeling, both with MNPs and with (111)In-oxine, did not affect DC phenotype or functionality. MRI and SPECT allowed the detection of iron and (111)In in both axillary and popliteal LNs. Immunohistochemistry and γ-counting revealed the presence of DCs in LNs.

CONCLUSIONS

MRI and SPECT imaging, by allowing in vivo dynamic monitoring of DC migration, could further the development and optimization of efficient anti-cancer vaccines.

摘要

目的

作者提出了一种方案,使用不同的成像技术,在一种鼠乳腺癌模型中评估肿瘤特异性树突状细胞(DC)向淋巴结(LN)归巢的体内情况。

过程

骨髓 DC 用顺磁纳米粒子(MNPs)或(111)In-oxine 标记。使用肿瘤裂解物进行抗原负载。成熟的 DC 被注射到转基因荷瘤小鼠(MMTV-Ras)的足垫中,并通过磁共振成像(MRI)和单光子发射计算机断层扫描(SPECT)跟踪 DC 迁移。进行了离体分析以验证成像数据。

结果

MNPs 和(111)In-oxine 标记的 DC 对 DC 表型或功能没有影响。MRI 和 SPECT 允许在腋窝和腘窝 LN 中检测到铁和(111)In。免疫组织化学和γ计数显示 LN 中存在 DC。

结论

MRI 和 SPECT 成像通过允许体内动态监测 DC 迁移,可进一步开发和优化有效的抗癌疫苗。

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