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抗ESAT-6单克隆抗体荧光探针在肺结核小鼠体内近红外荧光成像中的应用。

The application of anti-ESAT-6 monoclonal antibody fluorescent probe in ex vivo near-infrared fluorescence imaging in mice with pulmonary tuberculosis.

作者信息

Feng Feng, Zhang Haoling, Zhu Zhaoqin, Li Cong, Shi Yuxin, Zhang Zhiyong

机构信息

Department of Radiology, Shanghai Public Health Clinical Center Affiliated to Fudan University, Shanghai, 201508, China.

出版信息

Luminescence. 2014 Sep;29(6):614-20. doi: 10.1002/bio.2593. Epub 2013 Oct 29.

DOI:10.1002/bio.2593
PMID:24170605
Abstract

Here, we aimed to assess the feasibility of anti-ESAT-6 monoclonal antibody (mAb) coupling with IR783 and rhodamine fluorescent probe in the detection of ESAT-6 expression in tuberculosis tissue of mice using near-infrared fluorescence imaging. IR783 and rhodamine were conjugated to the anti-ESAT-6 mAb or IgG. Mice in the experimental group were injected with fluorescence-labeled mAb probe, and mice in the control group were injected with fluorescence-labeled non-specific IgG antibody. Twenty-four hours later, the lung tissue of mice was examined using ex vivo near-infrared fluorescence imaging. In addition, the contrast-to-noise ratio (CNR) was calculated by measuring the signal intensities of the pulmonary lesions, normal lung tissue and background noise. The frozen lung tissue section was examined under fluorescence microscopy and compared with hemoxylin and eosin (HE) staining. The ex vivo near-infrared fluorescence imaging showed that the fluorescence signal in the lung tuberculosis lesions in the experimental group was significantly enhanced, whereas there was only a weak fluorescence signal or even no fluorescence signal in the control group. CNR values were 64.40 ± 7.02 (n = 6) and 8.75 ± 3.87 (n = 6), respectively (t = 17.01, p < 0.001). The fluorescence accumulation distribution detected under fluorescence microscopy was consistent with HE staining of the tuberculosis region. In conclusion, anti-ESAT-6 mAb fluorescent probe could target and be applied in specific ex vivo imaging of mice tuberculosis, and may be of further use in tuberculosis in living mice.

摘要

在此,我们旨在评估抗ESAT-6单克隆抗体(mAb)与IR783及罗丹明荧光探针偶联,利用近红外荧光成像检测小鼠结核组织中ESAT-6表达的可行性。将IR783和罗丹明与抗ESAT-6 mAb或IgG偶联。实验组小鼠注射荧光标记的mAb探针,对照组小鼠注射荧光标记的非特异性IgG抗体。24小时后,使用离体近红外荧光成像检查小鼠的肺组织。此外,通过测量肺部病变、正常肺组织及背景噪声的信号强度来计算对比噪声比(CNR)。对冷冻肺组织切片进行荧光显微镜检查,并与苏木精和伊红(HE)染色结果进行比较。离体近红外荧光成像显示,实验组小鼠肺结核病变中的荧光信号显著增强,而对照组仅有微弱荧光信号甚至无荧光信号。CNR值分别为64.40±7.02(n = 6)和8.75±3.87(n = 6)(t = 17.01,p < 0.001)。荧光显微镜下检测到的荧光积聚分布与结核区域的HE染色结果一致。总之,抗ESAT-6 mAb荧光探针可靶向并应用于小鼠结核的特异性离体成像,可能在活体小鼠结核病检测中具有进一步应用价值。

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